Showing 141 - 160 results of 53,881 for search '(((( i values decrease ) OR ( ((30 days) OR (5 days)) increased ))) OR ( c large decrease ))', query time: 1.77s Refine Results
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    Table1_Oral anticoagulants increased 30-day survival in sepsis patients complicated with atrial fibrillation: a retrospective analysis from MIMIC-IV database.docx by Gaoyuan Ge (3764446)

    Published 2024
    “…Septic patients with no AF were considered as the control group (n = 5,873, sepsis and no AF group). The main outcome endpoint was the survival rate of 30 day. …”
  12. 152

    Table3_Oral anticoagulants increased 30-day survival in sepsis patients complicated with atrial fibrillation: a retrospective analysis from MIMIC-IV database.docx by Gaoyuan Ge (3764446)

    Published 2024
    “…Septic patients with no AF were considered as the control group (n = 5,873, sepsis and no AF group). The main outcome endpoint was the survival rate of 30 day. …”
  13. 153

    Table2_Oral anticoagulants increased 30-day survival in sepsis patients complicated with atrial fibrillation: a retrospective analysis from MIMIC-IV database.docx by Gaoyuan Ge (3764446)

    Published 2024
    “…Septic patients with no AF were considered as the control group (n = 5,873, sepsis and no AF group). The main outcome endpoint was the survival rate of 30 day. …”
  14. 154

    Image1_Oral anticoagulants increased 30-day survival in sepsis patients complicated with atrial fibrillation: a retrospective analysis from MIMIC-IV database.tif by Gaoyuan Ge (3764446)

    Published 2024
    “…Septic patients with no AF were considered as the control group (n = 5,873, sepsis and no AF group). The main outcome endpoint was the survival rate of 30 day. …”
  15. 155

    Image2_Oral anticoagulants increased 30-day survival in sepsis patients complicated with atrial fibrillation: a retrospective analysis from MIMIC-IV database.tif by Gaoyuan Ge (3764446)

    Published 2024
    “…Septic patients with no AF were considered as the control group (n = 5,873, sepsis and no AF group). The main outcome endpoint was the survival rate of 30 day. …”
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