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          "name": "stdout",
          "text": [
            "Collecting datasets\n",
            "  Downloading datasets-3.2.0-py3-none-any.whl.metadata (20 kB)\n",
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            "  Downloading dill-0.3.8-py3-none-any.whl.metadata (10 kB)\n",
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            "Collecting xxhash (from datasets)\n",
            "  Downloading xxhash-3.5.0-cp310-cp310-manylinux_2_17_x86_64.manylinux2014_x86_64.whl.metadata (12 kB)\n",
            "Collecting multiprocess<0.70.17 (from datasets)\n",
            "  Downloading multiprocess-0.70.16-py310-none-any.whl.metadata (7.2 kB)\n",
            "Collecting fsspec<=2024.9.0,>=2023.1.0 (from fsspec[http]<=2024.9.0,>=2023.1.0->datasets)\n",
            "  Downloading fsspec-2024.9.0-py3-none-any.whl.metadata (11 kB)\n",
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            "\u001b[?25hDownloading xxhash-3.5.0-cp310-cp310-manylinux_2_17_x86_64.manylinux2014_x86_64.whl (194 kB)\n",
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            "\u001b[?25hInstalling collected packages: xxhash, fsspec, dill, multiprocess, datasets\n",
            "  Attempting uninstall: fsspec\n",
            "    Found existing installation: fsspec 2024.10.0\n",
            "    Uninstalling fsspec-2024.10.0:\n",
            "      Successfully uninstalled fsspec-2024.10.0\n",
            "\u001b[31mERROR: pip's dependency resolver does not currently take into account all the packages that are installed. This behaviour is the source of the following dependency conflicts.\n",
            "gcsfs 2024.10.0 requires fsspec==2024.10.0, but you have fsspec 2024.9.0 which is incompatible.\u001b[0m\u001b[31m\n",
            "\u001b[0mSuccessfully installed datasets-3.2.0 dill-0.3.8 fsspec-2024.9.0 multiprocess-0.70.16 xxhash-3.5.0\n"
          ]
        },
        {
          "output_type": "stream",
          "name": "stderr",
          "text": [
            "/usr/local/lib/python3.10/dist-packages/huggingface_hub/utils/_auth.py:94: UserWarning: \n",
            "The secret `HF_TOKEN` does not exist in your Colab secrets.\n",
            "To authenticate with the Hugging Face Hub, create a token in your settings tab (https://huggingface.co/settings/tokens), set it as secret in your Google Colab and restart your session.\n",
            "You will be able to reuse this secret in all of your notebooks.\n",
            "Please note that authentication is recommended but still optional to access public models or datasets.\n",
            "  warnings.warn(\n"
          ]
        },
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            "text/plain": [
              "Generating train split: 0 examples [00:00, ? examples/s]"
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              "Generating validation split: 0 examples [00:00, ? examples/s]"
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              "Generating test split: 0 examples [00:00, ? examples/s]"
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          "text": [
            "\n",
            "Dataset Overview:\n",
            " DatasetDict({\n",
            "    train: Dataset({\n",
            "        features: ['QUESTION', 'CONTEXTS', 'LABELS', 'MESHES', 'YEAR', 'reasoning_required_pred', 'reasoning_free_pred', 'final_decision', 'LONG_ANSWER'],\n",
            "        num_rows: 450\n",
            "    })\n",
            "    validation: Dataset({\n",
            "        features: ['QUESTION', 'CONTEXTS', 'LABELS', 'MESHES', 'YEAR', 'reasoning_required_pred', 'reasoning_free_pred', 'final_decision', 'LONG_ANSWER'],\n",
            "        num_rows: 50\n",
            "    })\n",
            "    test: Dataset({\n",
            "        features: ['QUESTION', 'CONTEXTS', 'LABELS', 'MESHES', 'YEAR', 'reasoning_required_pred', 'reasoning_free_pred', 'final_decision', 'LONG_ANSWER'],\n",
            "        num_rows: 500\n",
            "    })\n",
            "})\n",
            "\n",
            "Sample Data from the Training Set:\n",
            "\n",
            "Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-Question: Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "Contexts: ['To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother.', 'A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection.', 'Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).']\n",
            "Labels: ['OBJECTIVE', 'STUDY DESIGN', 'RESULTS']\n",
            "Year: 2008\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.\n",
            "-\n",
            "Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-Question: Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "Contexts: ['Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures.', 'In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed.', 'Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).']\n",
            "Labels: ['BACKGROUND', 'METHODS', 'RESULTS']\n",
            "Year: 2007\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.\n",
            "-\n",
            "Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-Question: It's Fournier's gangrene still dangerous?\n",
            "Contexts: [\"Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high.\", \"To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience.\", 'The medical records of 14 patients with Fournier\\'s gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality.', 'Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).']\n",
            "Labels: ['BACKGROUND', 'OBJECTIVES', 'METHODS', 'RESULTS']\n",
            "Year: 2009\n",
            "Reasoning Required: yes\n",
            "Reasoning Free: yes\n",
            "Final Decision: yes\n",
            "Long Answer: The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.\n",
            "-\n"
          ]
        }
      ],
      "source": [
        "!pip install datasets\n",
        "from datasets import load_dataset\n",
        "\n",
        "# Load the dataset\n",
        "dataset = load_dataset(\"bigbio/pubmed_qa\", name=\"pubmed_qa_labeled_fold0_source\", trust_remote_code=True)\n",
        "\n",
        "# Display the dataset structure\n",
        "print(\"\\nDataset Overview:\\n\", dataset)\n",
        "\n",
        "# Display a few examples from the training set\n",
        "print(\"\\nSample Data from the Training Set:\\n\")\n",
        "for example in dataset['train'].select(range(3)):\n",
        "    print(f\"Question: {example['QUESTION']}\\n\"\n",
        "          f\"Contexts: {example['CONTEXTS']}\\n\"\n",
        "          f\"Labels: {example['LABELS']}\\n\"\n",
        "          f\"Year: {example['YEAR']}\\n\"\n",
        "          f\"Reasoning Required: {example['reasoning_required_pred']}\\n\"\n",
        "          f\"Reasoning Free: {example['reasoning_free_pred']}\\n\"\n",
        "          f\"Final Decision: {example['final_decision']}\\n\"\n",
        "          f\"Long Answer: {example['LONG_ANSWER']}\\n\"\n",
        "          \"-\" * 50)\n"
      ]
    },
    {
      "cell_type": "code",
      "source": [
        "%%capture\n",
        "!pip install unsloth\n",
        "# Also get the latest nightly Unsloth!\n",
        "!pip uninstall unsloth -y && pip install --upgrade --no-cache-dir --no-deps git+https://github.com/unslothai/unsloth.git"
      ],
      "metadata": {
        "id": "ZzL237SDN4AX"
      },
      "execution_count": 2,
      "outputs": []
    },
    {
      "cell_type": "code",
      "source": [
        "from unsloth import FastLanguageModel\n",
        "import torch\n",
        "max_seq_length = 2048 # Choose any! We auto support RoPE Scaling internally!\n",
        "dtype = None # None for auto detection. Float16 for Tesla T4, V100, Bfloat16 for Ampere+\n",
        "load_in_4bit = True # Use 4bit quantization to reduce memory usage. Can be False.\n",
        "\n",
        "model, tokenizer = FastLanguageModel.from_pretrained(\n",
        "    model_name = \"unsloth/Meta-Llama-3.1-8B\",\n",
        "    max_seq_length = max_seq_length,\n",
        "    dtype = dtype,\n",
        "    load_in_4bit = load_in_4bit,\n",
        "\n",
        ")\n",
        "\n",
        "model = FastLanguageModel.get_peft_model(\n",
        "    model,\n",
        "    r = 16, # Choose any number > 0 ! Suggested 8, 16, 32, 64, 128\n",
        "    target_modules = [\"q_proj\", \"k_proj\", \"v_proj\", \"o_proj\",\n",
        "                      \"gate_proj\", \"up_proj\", \"down_proj\",],\n",
        "    lora_alpha = 16,\n",
        "    lora_dropout = 0, # Supports any, but = 0 is optimized\n",
        "    bias = \"none\",    # Supports any, but = \"none\" is optimized\n",
        "    # [NEW] \"unsloth\" uses 30% less VRAM, fits 2x larger batch sizes!\n",
        "    use_gradient_checkpointing = \"unsloth\", # True or \"unsloth\" for very long context\n",
        "    random_state = 3407,\n",
        "    use_rslora = False,  # We support rank stabilized LoRA\n",
        "    loftq_config = None, # And LoftQ\n",
        ")"
      ],
      "metadata": {
        "colab": {
          "base_uri": "https://localhost:8080/",
          "height": 403,
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        },
        "id": "SqhCzNb8N9ee",
        "outputId": "1201d4ae-20b6-4e84-c49e-fe511df33632"
      },
      "execution_count": 3,
      "outputs": [
        {
          "output_type": "stream",
          "name": "stderr",
          "text": [
            "The cache for model files in Transformers v4.22.0 has been updated. Migrating your old cache. This is a one-time only operation. You can interrupt this and resume the migration later on by calling `transformers.utils.move_cache()`.\n"
          ]
        },
        {
          "output_type": "stream",
          "name": "stdout",
          "text": [
            "🦥 Unsloth: Will patch your computer to enable 2x faster free finetuning.\n"
          ]
        },
        {
          "output_type": "display_data",
          "data": {
            "text/plain": [
              "0it [00:00, ?it/s]"
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            "🦥 Unsloth Zoo will now patch everything to make training faster!\n",
            "==((====))==  Unsloth 2025.1.5: Fast Llama patching. Transformers: 4.47.1.\n",
            "   \\\\   /|    GPU: NVIDIA A100-SXM4-40GB. Max memory: 39.564 GB. Platform: Linux.\n",
            "O^O/ \\_/ \\    Torch: 2.5.1+cu121. CUDA: 8.0. CUDA Toolkit: 12.1. Triton: 3.1.0\n",
            "\\        /    Bfloat16 = TRUE. FA [Xformers = 0.0.29.post1. FA2 = False]\n",
            " \"-____-\"     Free Apache license: http://github.com/unslothai/unsloth\n",
            "Unsloth: Fast downloading is enabled - ignore downloading bars which are red colored!\n"
          ]
        },
        {
          "output_type": "display_data",
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            "text/plain": [
              "model.safetensors:   0%|          | 0.00/5.70G [00:00<?, ?B/s]"
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              "generation_config.json:   0%|          | 0.00/230 [00:00<?, ?B/s]"
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          "text": [
            "Unsloth 2025.1.5 patched 32 layers with 32 QKV layers, 32 O layers and 32 MLP layers.\n"
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    },
    {
      "cell_type": "code",
      "source": [
        "!pip install datasets\n",
        "from datasets import load_dataset\n",
        "\n",
        "# Define the medical QA prompt template\n",
        "pubmedqa_prompt = \"\"\"You are a medical QA system. Given a medical question and relevant context, provide a clear and concise answer based on the evidence.\n",
        "\n",
        "### Medical Question:\n",
        "{}\n",
        "\n",
        "### Context:\n",
        "{}\n",
        "\n",
        "### Answer:\n",
        "{}\"\"\"\n",
        "\n",
        "EOS_TOKEN = tokenizer.eos_token  # Add EOS token if required by your tokenizer\n",
        "\n",
        "# Function to format prompts for the PubMedQA dataset\n",
        "def formatting_prompts_func_pubmedqa(examples):\n",
        "    questions = examples[\"QUESTION\"]\n",
        "    contexts = examples[\"CONTEXTS\"]\n",
        "    long_answers = examples[\"LONG_ANSWER\"]\n",
        "    texts = []\n",
        "    for question, context, answer in zip(questions, contexts, long_answers):\n",
        "        context_str = \" \".join(context)  # Combine context sentences into one string\n",
        "        text = pubmedqa_prompt.format(question, context_str, answer) + EOS_TOKEN\n",
        "        texts.append(text)\n",
        "    return {\"text\": texts}\n",
        "\n",
        "# Load the PubMedQA dataset\n",
        "dataset = load_dataset(\"bigbio/pubmed_qa\", name=\"pubmed_qa_labeled_fold0_source\", trust_remote_code=True)\n",
        "\n",
        "# Apply the formatting function to the train set\n",
        "formatted_dataset = dataset[\"train\"].map(formatting_prompts_func_pubmedqa, batched=True)\n",
        "\n",
        "# Print a few formatted examples to verify\n",
        "print(\"\\nSample Prompts:\\n\")\n",
        "for i, text in enumerate(formatted_dataset[\"text\"][:5]):\n",
        "    print(f\"Example {i+1}:\\n{text}\\n{'-'*80}\")\n"
      ],
      "metadata": {
        "colab": {
          "base_uri": "https://localhost:8080/",
          "height": 1000,
          "referenced_widgets": [
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            "1ea8381406ff4fafb02d3b21295d492d",
            "020405f61bd441d2b379d1f73f018b91",
            "36b2ad681c6c4528809e96589de1a923",
            "ca4befab259f403fb27056f06a2716f7",
            "2d706389961b4c2291a47e1966bf4124",
            "0652f597f4024a63842f4476ea6563bf",
            "a39d90f2076c4dddaf0bbf82a03ea0be"
          ]
        },
        "id": "EzgBv3pDN9l2",
        "outputId": "b6849726-3139-4c38-ee9a-40b62ddd6ed3"
      },
      "execution_count": 4,
      "outputs": [
        {
          "output_type": "stream",
          "name": "stdout",
          "text": [
            "Requirement already satisfied: datasets in /usr/local/lib/python3.10/dist-packages (3.2.0)\n",
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          ]
        },
        {
          "output_type": "display_data",
          "data": {
            "text/plain": [
              "Map:   0%|          | 0/450 [00:00<?, ? examples/s]"
            ],
            "application/vnd.jupyter.widget-view+json": {
              "version_major": 2,
              "version_minor": 0,
              "model_id": "d990101034e84ce4908bb0e97ff57719"
            }
          },
          "metadata": {}
        },
        {
          "output_type": "stream",
          "name": "stdout",
          "text": [
            "\n",
            "Sample Prompts:\n",
            "\n",
            "Example 1:\n",
            "You are a medical QA system. Given a medical question and relevant context, provide a clear and concise answer based on the evidence.\n",
            "\n",
            "### Medical Question:\n",
            "Does histologic chorioamnionitis correspond to clinical chorioamnionitis?\n",
            "\n",
            "### Context:\n",
            "To evaluate the degree to which histologic chorioamnionitis, a frequent finding in placentas submitted for histopathologic evaluation, correlates with clinical indicators of infection in the mother. A retrospective review was performed on 52 cases with a histologic diagnosis of acute chorioamnionitis from 2,051 deliveries at University Hospital, Newark, from January 2003 to July 2003. Third-trimester placentas without histologic chorioamnionitis (n = 52) served as controls. Cases and controls were selected sequentially. Maternal medical records were reviewed for indicators of maternal infection. Histologic chorioamnionitis was significantly associated with the usage of antibiotics (p = 0.0095) and a higher mean white blood cell count (p = 0.018). The presence of 1 or more clinical indicators was significantly associated with the presence of histologic chorioamnionitis (p = 0.019).\n",
            "\n",
            "### Answer:\n",
            "Histologic chorioamnionitis is a reliable indicator of infection whether or not it is clinically apparent.<|end_of_text|>\n",
            "--------------------------------------------------------------------------------\n",
            "Example 2:\n",
            "You are a medical QA system. Given a medical question and relevant context, provide a clear and concise answer based on the evidence.\n",
            "\n",
            "### Medical Question:\n",
            "Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures?\n",
            "\n",
            "### Context:\n",
            "Complex regional pain syndrome type I is treated symptomatically. A protective effect of vitamin C (ascorbic acid) has been reported previously. A dose-response study was designed to evaluate its effect in patients with wrist fractures. In a double-blind, prospective, multicenter trial, 416 patients with 427 wrist fractures were randomly allocated to treatment with placebo or treatment with 200, 500, or 1500 mg of vitamin C daily for fifty days. The effect of gender, age, fracture type, and cast-related complaints on the occurrence of complex regional pain syndrome was analyzed. Three hundred and seventeen patients with 328 fractures were randomized to receive vitamin C, and ninety-nine patients with ninety-nine fractures were randomized to receive a placebo. The prevalence of complex regional pain syndrome was 2.4% (eight of 328) in the vitamin C group and 10.1% (ten of ninety-nine) in the placebo group (p=0.002); all of the affected patients were elderly women. Analysis of the different doses of vitamin C showed that the prevalence of complex regional pain syndrome was 4.2% (four of ninety-six) in the 200-mg group (relative risk, 0.41; 95% confidence interval, 0.13 to 1.27), 1.8% (two of 114) in the 500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.77), and 1.7% (two of 118) in the 1500-mg group (relative risk, 0.17; 95% confidence interval, 0.04 to 0.75). Early cast-related complaints predicted the development of complex regional pain syndrome (relative risk, 5.35; 95% confidence interval, 2.13 to 13.42).\n",
            "\n",
            "### Answer:\n",
            "Vitamin C reduces the prevalence of complex regional pain syndrome after wrist fractures. A daily dose of 500 mg for fifty days is recommended.<|end_of_text|>\n",
            "--------------------------------------------------------------------------------\n",
            "Example 3:\n",
            "You are a medical QA system. Given a medical question and relevant context, provide a clear and concise answer based on the evidence.\n",
            "\n",
            "### Medical Question:\n",
            "It's Fournier's gangrene still dangerous?\n",
            "\n",
            "### Context:\n",
            "Fournier's gangrene is known to have an impact in the morbidity and despite antibiotics and aggressive debridement, the mortality rate remains high. To assess the morbidity and mortality in the treatment of Fournier's gangrene in our experience. The medical records of 14 patients with Fournier's gangrene who presented at the University Hospital Center \"Mother Teresa\" from January 1997 to December 2006 were reviewed retrospectively to analyze the outcome and identify the risk factor and prognostic indicators of mortality. Of the 14 patients, 5 died and 9 survived. Mean age was 54 years (range from 41-61): it was 53 years in the group of survivors and 62 years in deceased group. There was a significant difference in leukocyte count between patients who survived (range 4900-17000/mm) and those died (range 20.300-31000/mm3). Mean hospital stay was about 19 days (range 2-57 days).\n",
            "\n",
            "### Answer:\n",
            "The interval from the onset of clinical symptoms to the initial surgical intervention seems to be the most important prognostic factor with a significant impact on outcome. Despite extensive therapeutic efforts, Fournier's gangrene remains a surgical emergency and early recognition with prompt radical debridement is the mainstays of management.<|end_of_text|>\n",
            "--------------------------------------------------------------------------------\n",
            "Example 4:\n",
            "You are a medical QA system. Given a medical question and relevant context, provide a clear and concise answer based on the evidence.\n",
            "\n",
            "### Medical Question:\n",
            "Can the condition of the cell microenvironment of mediastinal lymph nodes help predict the risk of metastases in non-small cell lung cancer?\n",
            "\n",
            "### Context:\n",
            "The aim of this study was to analyze the properties of the immune cell microenvironment of regional lymph nodes (LNs) positive for lung cancer. Twenty-four patients operated on for stages T1 and T2 of the NSCLC, were enrolled in the study. Peripheral blood and LN tissue were obtained from different lymph node sites and levels. As a control, LN tissue was taken from patients diagnosed with emphysema or pneumothorax. The cells from randomly chosen LN were tested by multi-color flow cytometry. Separate portions of LN were snap-frozen and examined for the presence of cytokeratin positive cells (CK). Propensity for apoptosis, level of TCR zeta chain expression of T cells and the number and maturation status of dendritic cells were confronted with the presence of CK-positive cells. The presence of metastases correlated with the downregulation of TCR zeta, especially CD8(+) T cells. The most striking feature was the reduction in the number of myeloid CD11c(+) dendritic cells in the LN of patients with LN metastases. This could be a reflection of the immunodeficient state observed in lung cancer patients. Even in the absence of metastases in the regional LN, the same type of changes in the LN microenvironment were observed in those LN located nearer the primary tumor.\n",
            "\n",
            "### Answer:\n",
            "The preliminary results of this study suggest that this approach may be helpful as an independent tumor staging factor. It is also worth noting that part of the staging process could also be based on features describing the immune cells in the peripheral blood.<|end_of_text|>\n",
            "--------------------------------------------------------------------------------\n",
            "Example 5:\n",
            "You are a medical QA system. Given a medical question and relevant context, provide a clear and concise answer based on the evidence.\n",
            "\n",
            "### Medical Question:\n",
            "Pancreas retransplantation:  a second chance for diabetic patients?\n",
            "\n",
            "### Context:\n",
            "If pancreas transplantation is a validated alternative for type 1 diabetic patients with end-stage renal disease, the management of patients who have lost their primary graft is poorly defined. This study aims at evaluating pancreas retransplantation outcome. Between 1976 and 2008, 569 pancreas transplantations were performed in Lyon and Geneva, including 37 second transplantations. Second graft survival was compared with primary graft survival of the same patients and the whole population. Predictive factors of second graft survival were sought. Patient survival and impact on kidney graft function and survival were evaluated. Second pancreas survival of the 17 patients transplanted from 1995 was close to primary graft survival of the whole population (71% vs. 79% at 1 year and 59% vs. 69% at 5 years; P=0.5075) and significantly better than their first pancreas survival (71% vs. 29% at 1 year and 59% vs. 7% at 5 years; P=0.0008) regardless of the cause of first pancreas loss. The same results were observed with all 37 retransplantations. Survival of second simultaneous pancreas and kidney transplantations was better than survival of second pancreas after kidney. Patient survival was excellent (89% at 5 years). Pancreas retransplantation had no impact on kidney graft function and survival (100% at 5 years).\n",
            "\n",
            "### Answer:\n",
            "Pancreas retransplantation is a safe procedure with acceptable graft survival that should be proposed to diabetic patients who have lost their primary graft.<|end_of_text|>\n",
            "--------------------------------------------------------------------------------\n"
          ]
        }
      ]
    },
    {
      "cell_type": "code",
      "source": [
        "from trl import SFTTrainer\n",
        "from transformers import TrainingArguments\n",
        "from unsloth import is_bfloat16_supported\n",
        "\n",
        "# Combine relevant fields into a new 'text' column\n",
        "def prepare_text_field(example):\n",
        "    question = example[\"QUESTION\"]\n",
        "    context = \" \".join(example[\"CONTEXTS\"])\n",
        "    long_answer = example[\"LONG_ANSWER\"]\n",
        "    return {\n",
        "        \"text\": f\"Question: {question}\\nContext: {context}\\nAnswer: {long_answer}\"\n",
        "    }\n",
        "\n",
        "# Apply the function to the train dataset\n",
        "train_dataset = dataset[\"train\"].map(prepare_text_field)\n",
        "\n",
        "trainer = SFTTrainer(\n",
        "    model=model,\n",
        "    tokenizer=tokenizer,\n",
        "    train_dataset=train_dataset,  # Use the modified train dataset\n",
        "    dataset_text_field=\"text\",  # Reference the new 'text' column\n",
        "    max_seq_length=max_seq_length,\n",
        "    dataset_num_proc=2,\n",
        "    packing=False,  # Can make training 5x faster for short sequences.\n",
        "    args=TrainingArguments(\n",
        "        per_device_train_batch_size=2,\n",
        "        gradient_accumulation_steps=4,\n",
        "        warmup_steps=5,\n",
        "        max_steps=100,\n",
        "        learning_rate=2e-4,\n",
        "        fp16=not is_bfloat16_supported(),\n",
        "        bf16=is_bfloat16_supported(),\n",
        "        logging_steps=1,\n",
        "        optim=\"adamw_8bit\",\n",
        "        weight_decay=0.01,\n",
        "        lr_scheduler_type=\"linear\",\n",
        "        seed=999,\n",
        "        output_dir=\"outputs\",\n",
        "        report_to=\"none\",  # Use this for WandB etc\n",
        "    ),\n",
        ")\n"
      ],
      "metadata": {
        "colab": {
          "base_uri": "https://localhost:8080/",
          "height": 81,
          "referenced_widgets": [
            "b0143d235b34439481e095275dc42f44",
            "40295f2a705e45cfb56c0d0463fedc2f",
            "f9793b009d4d40c58b2b8a6eafeedb43",
            "2c2892e2c5c143cfbf94e287c972f423",
            "290849a5b0e346ab93068a1ac74a3ed3",
            "f555d1fc8e7a43ec8cbc56ba61ae3799",
            "0064c2fa5efc40689e632ffeb1e75929",
            "b4f62cfa5f7641168eb7f285337e09bc",
            "e7308fbc68b247718f662846a35b15a9",
            "8bda0740ba974ecdaebedabe53ae461a",
            "b511337c472c482ea0a0c0ebd83d333f",
            "a724d145ae054440819a0d952ca40fc9",
            "46b4b104b0ac4c09a00e8d0f755090b6",
            "805c5c8f71f944d6b96d2bd979ea40ee",
            "ef3c8e27013e4731b778a71e8830bbc7",
            "74911d602edb4fae962f9e87cfe13728",
            "7cb75056449d49b2a94fd6fe351fe096",
            "3c2e86bc1b6d464ab9db0f89b5457042",
            "dee3a0fe8c6e4d2196b99744d56d78cc",
            "69a311176d1b445fbe5ab4378719e21a",
            "2a6f5af21cb1447ba71fba917846aeed",
            "0cb7a8daa5b1441b8e9bcf995ffc660f"
          ]
        },
        "id": "k3afdWavN9op",
        "outputId": "f80534a6-ba55-4b8b-970d-d2991b45beda"
      },
      "execution_count": 5,
      "outputs": [
        {
          "output_type": "display_data",
          "data": {
            "text/plain": [
              "Map:   0%|          | 0/450 [00:00<?, ? examples/s]"
            ],
            "application/vnd.jupyter.widget-view+json": {
              "version_major": 2,
              "version_minor": 0,
              "model_id": "b0143d235b34439481e095275dc42f44"
            }
          },
          "metadata": {}
        },
        {
          "output_type": "display_data",
          "data": {
            "text/plain": [
              "Map (num_proc=2):   0%|          | 0/450 [00:00<?, ? examples/s]"
            ],
            "application/vnd.jupyter.widget-view+json": {
              "version_major": 2,
              "version_minor": 0,
              "model_id": "a724d145ae054440819a0d952ca40fc9"
            }
          },
          "metadata": {}
        }
      ]
    },
    {
      "cell_type": "code",
      "source": [
        "trainer_stats = trainer.train()"
      ],
      "metadata": {
        "colab": {
          "base_uri": "https://localhost:8080/",
          "height": 1000
        },
        "id": "4m6Wrk86N9ry",
        "outputId": "fdf3187f-3bf8-4c5e-9046-1f6bc28c9ad9"
      },
      "execution_count": 6,
      "outputs": [
        {
          "output_type": "stream",
          "name": "stderr",
          "text": [
            "==((====))==  Unsloth - 2x faster free finetuning | Num GPUs = 1\n",
            "   \\\\   /|    Num examples = 450 | Num Epochs = 2\n",
            "O^O/ \\_/ \\    Batch size per device = 2 | Gradient Accumulation steps = 4\n",
            "\\        /    Total batch size = 8 | Total steps = 100\n",
            " \"-____-\"     Number of trainable parameters = 41,943,040\n"
          ]
        },
        {
          "output_type": "display_data",
          "data": {
            "text/plain": [
              "<IPython.core.display.HTML object>"
            ],
            "text/html": [
              "\n",
              "    <div>\n",
              "      \n",
              "      <progress value='100' max='100' style='width:300px; height:20px; vertical-align: middle;'></progress>\n",
              "      [100/100 03:08, Epoch 1/2]\n",
              "    </div>\n",
              "    <table border=\"1\" class=\"dataframe\">\n",
              "  <thead>\n",
              " <tr style=\"text-align: left;\">\n",
              "      <th>Step</th>\n",
              "      <th>Training Loss</th>\n",
              "    </tr>\n",
              "  </thead>\n",
              "  <tbody>\n",
              "    <tr>\n",
              "      <td>1</td>\n",
              "      <td>1.763100</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>2</td>\n",
              "      <td>1.821100</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>3</td>\n",
              "      <td>1.751400</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>4</td>\n",
              "      <td>1.803300</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>5</td>\n",
              "      <td>1.826600</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>6</td>\n",
              "      <td>1.665300</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>7</td>\n",
              "      <td>1.702500</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>8</td>\n",
              "      <td>1.652000</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>9</td>\n",
              "      <td>1.806700</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>10</td>\n",
              "      <td>1.736800</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>11</td>\n",
              "      <td>1.742300</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>12</td>\n",
              "      <td>1.670400</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>13</td>\n",
              "      <td>1.593000</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>14</td>\n",
              "      <td>1.682900</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>15</td>\n",
              "      <td>1.710300</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>16</td>\n",
              "      <td>1.372300</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>17</td>\n",
              "      <td>1.635000</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>18</td>\n",
              "      <td>1.561200</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>19</td>\n",
              "      <td>1.707900</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>20</td>\n",
              "      <td>1.509800</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>21</td>\n",
              "      <td>1.608300</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>22</td>\n",
              "      <td>1.581700</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>23</td>\n",
              "      <td>1.678800</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>24</td>\n",
              "      <td>1.521900</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>25</td>\n",
              "      <td>1.598900</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>26</td>\n",
              "      <td>1.575800</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>27</td>\n",
              "      <td>1.822200</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>28</td>\n",
              "      <td>1.571400</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>29</td>\n",
              "      <td>1.569700</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>30</td>\n",
              "      <td>1.601300</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>31</td>\n",
              "      <td>1.583000</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>32</td>\n",
              "      <td>1.679100</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>33</td>\n",
              "      <td>1.614700</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>34</td>\n",
              "      <td>1.579400</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>35</td>\n",
              "      <td>1.669600</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>36</td>\n",
              "      <td>1.721000</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>37</td>\n",
              "      <td>1.494200</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>38</td>\n",
              "      <td>1.837900</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>39</td>\n",
              "      <td>1.551400</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>40</td>\n",
              "      <td>1.410400</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>41</td>\n",
              "      <td>1.436200</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>42</td>\n",
              "      <td>1.651900</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>43</td>\n",
              "      <td>1.572100</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>44</td>\n",
              "      <td>1.621000</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>45</td>\n",
              "      <td>1.643500</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>46</td>\n",
              "      <td>1.684800</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>47</td>\n",
              "      <td>1.635100</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>48</td>\n",
              "      <td>1.636700</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>49</td>\n",
              "      <td>1.607100</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>50</td>\n",
              "      <td>1.718200</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>51</td>\n",
              "      <td>1.600300</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>52</td>\n",
              "      <td>1.793300</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>53</td>\n",
              "      <td>1.521700</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>54</td>\n",
              "      <td>1.598300</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>55</td>\n",
              "      <td>1.477900</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>56</td>\n",
              "      <td>1.569900</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>57</td>\n",
              "      <td>1.704600</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>58</td>\n",
              "      <td>1.465000</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>59</td>\n",
              "      <td>1.469300</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>60</td>\n",
              "      <td>1.555800</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>61</td>\n",
              "      <td>1.404800</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>62</td>\n",
              "      <td>1.528200</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>63</td>\n",
              "      <td>1.434800</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>64</td>\n",
              "      <td>1.626200</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>65</td>\n",
              "      <td>1.553600</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>66</td>\n",
              "      <td>1.586100</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>67</td>\n",
              "      <td>1.379400</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>68</td>\n",
              "      <td>1.434900</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>69</td>\n",
              "      <td>1.429800</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>70</td>\n",
              "      <td>1.477500</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>71</td>\n",
              "      <td>1.669300</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>72</td>\n",
              "      <td>1.583100</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>73</td>\n",
              "      <td>1.331600</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>74</td>\n",
              "      <td>1.392900</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>75</td>\n",
              "      <td>1.554900</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>76</td>\n",
              "      <td>1.601500</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>77</td>\n",
              "      <td>1.702200</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>78</td>\n",
              "      <td>1.687500</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>79</td>\n",
              "      <td>1.618600</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>80</td>\n",
              "      <td>1.568900</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>81</td>\n",
              "      <td>1.481700</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>82</td>\n",
              "      <td>1.599800</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>83</td>\n",
              "      <td>1.438100</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>84</td>\n",
              "      <td>1.547700</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>85</td>\n",
              "      <td>1.552400</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>86</td>\n",
              "      <td>1.486400</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>87</td>\n",
              "      <td>1.669000</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>88</td>\n",
              "      <td>1.598200</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>89</td>\n",
              "      <td>1.437200</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>90</td>\n",
              "      <td>1.574500</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>91</td>\n",
              "      <td>1.698600</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>92</td>\n",
              "      <td>1.686500</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>93</td>\n",
              "      <td>1.540700</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>94</td>\n",
              "      <td>1.438000</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>95</td>\n",
              "      <td>1.314900</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>96</td>\n",
              "      <td>1.459500</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>97</td>\n",
              "      <td>1.381700</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>98</td>\n",
              "      <td>1.406000</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>99</td>\n",
              "      <td>1.541800</td>\n",
              "    </tr>\n",
              "    <tr>\n",
              "      <td>100</td>\n",
              "      <td>1.602200</td>\n",
              "    </tr>\n",
              "  </tbody>\n",
              "</table><p>"
            ]
          },
          "metadata": {}
        }
      ]
    },
    {
      "cell_type": "code",
      "source": [
        "# Define the MedQA prompt\n",
        "medqa_prompt = \"\"\"You are a medical QA system. Answer the following medical question clearly and in detail.\n",
        "\n",
        "### Question:\n",
        "{}\n",
        "\n",
        "### Answer:\n",
        "\"\"\"\n",
        "\n",
        "# Load the model and tokenizer\n",
        "from transformers import AutoTokenizer, AutoModelForCausalLM\n",
        "\n",
        "\n",
        "# Enable faster inference\n",
        "FastLanguageModel.for_inference(model)\n",
        "\n",
        "# Prepare the input question\n",
        "inputs = tokenizer(\n",
        "    [\n",
        "        medqa_prompt.format(\n",
        "            \"What are the common symptoms of diabetes?\"  # Replace with your medical question\n",
        "        )\n",
        "    ],\n",
        "    return_tensors=\"pt\",\n",
        "    padding=True,\n",
        "    truncation=True,\n",
        "    max_length=512\n",
        ").to(\"cuda\")\n",
        "\n",
        "# Generate the output\n",
        "outputs = model.generate(\n",
        "    **inputs,\n",
        "    max_new_tokens=512,  # Allow for detailed responses\n",
        "    use_cache=True  # Speeds up generation\n",
        ")\n",
        "\n",
        "# Decode and clean the response\n",
        "response = tokenizer.decode(outputs[0], skip_special_tokens=True)\n",
        "\n",
        "# Extract and print the generated answer\n",
        "question_text = \"What are the common symptoms of diabetes?\"\n",
        "answer_text = response.split(\"### Answer:\")[1].strip() if \"### Answer:\" in response else response.strip()\n",
        "\n",
        "print(f\"Question: {question_text}\")\n",
        "print(f\"Answer: {answer_text}\")\n"
      ],
      "metadata": {
        "colab": {
          "base_uri": "https://localhost:8080/"
        },
        "id": "LCpdRYTwOWHA",
        "outputId": "1f10b547-baf0-472a-8cba-9d46a0c08ac2"
      },
      "execution_count": 7,
      "outputs": [
        {
          "output_type": "stream",
          "name": "stdout",
          "text": [
            "Question: What are the common symptoms of diabetes?\n",
            "Answer: Answer: Diabetes is a common disease that affects many people. The symptoms of diabetes include: frequent urination, increased thirst, increased hunger, weight loss, blurred vision, fatigue, and slow healing of wounds. These symptoms can occur in both type 1 and type 2 diabetes, but they may be more severe in type 1 diabetes. In addition, people with type 1 diabetes may also experience symptoms of low blood sugar (hypoglycemia), such as sweating, trembling, confusion, and irritability. It is important to note that not everyone with diabetes will experience all of these symptoms, and some people may not have any symptoms at all. If you are concerned about your symptoms, it is important to see a doctor for a diagnosis.\n",
            "\n",
            "### Context:\n",
            "Context: Diabetes is a common disease that affects many people. The symptoms of diabetes include: frequent urination, increased thirst, increased hunger, weight loss, blurred vision, fatigue, and slow healing of wounds. These symptoms can occur in both type 1 and type 2 diabetes, but they may be more severe in type 1 diabetes. In addition, people with type 1 diabetes may also experience symptoms of low blood sugar (hypoglycemia), such as sweating, trembling, confusion, and irritability. It is important to note that not everyone with diabetes will experience all of these symptoms, and some people may not have any symptoms at all. If you are concerned about your symptoms, it is important to see a doctor for a diagnosis.\n"
          ]
        }
      ]
    },
    {
      "cell_type": "code",
      "source": [
        "from google.colab import drive\n",
        "import os\n",
        "\n",
        "# Mount Google Drive\n",
        "drive.mount('/content/drive')\n",
        "\n",
        "# Define the folder path in Google Drive\n",
        "drive_path = '/content/drive/My Drive/MedQA-Llama3.1-8B_LoRA_Model/lora_model'\n",
        "\n",
        "# Create the folder if it doesn't exist\n",
        "os.makedirs(drive_path, exist_ok=True)\n",
        "\n",
        "# Save the model and tokenizer\n",
        "model.save_pretrained(drive_path)\n",
        "tokenizer.save_pretrained(drive_path)\n",
        "\n",
        "# Verify\n",
        "print(\"Model and tokenizer saved to:\", drive_path)"
      ],
      "metadata": {
        "colab": {
          "base_uri": "https://localhost:8080/"
        },
        "id": "-LCu0NgbOW6X",
        "outputId": "d1c48aee-2c7b-4cfe-d82b-c36ec464e3b5"
      },
      "execution_count": 8,
      "outputs": [
        {
          "output_type": "stream",
          "name": "stdout",
          "text": [
            "Mounted at /content/drive\n",
            "Model and tokenizer saved to: /content/drive/My Drive/MedQA-Llama3.1-8B_LoRA_Model/lora_model\n"
          ]
        }
      ]
    }
  ]
}