Bleeding disorders and risk

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Incomplete information; this section will be expanded, clarified, and with references added in the future.

Initial evaluation

  • Bleeding history (acquired or inherited disorder?)
    • Spontaneous or provoked by surgery, tooth extraction, etc.
    • Tolerance of prior surgery
    • Menses
    • Mucocutaneous bleeding, petechiae, oozing at line sites
    • Bruising, hemarthrosis
    • Family history--known hemophilia A, hemophilia B, von Willebrand disease (VWD), platelet function disorder
    • Need for transfusion or product
  • History of trauma, surgery
  • PT/INR
  • PTT
  • Platelet count
  • +/- fibrinogen (DIC), D-dimer, fibrin/fibrinogen degradation products (FDP)
  • Kidney disease (uremia)
  • Medications: anticoagulants, antiplatelet medications such as aspirin and Clopidogrel (Plavix), NSAIDS, antidepressants which cause decrease in platelet function

Abnormal PT/INR or PTT

  • 1:1 mixing study (50/50 mixing study, circulating anticoagulant)
  • Liver disease
  • Elevated PT only
    • Vitamin K deficiency
      • Warfarin
      • Dietary habits
      • Antibiotic use
      • Malnutrition
      • Increased gut motility
    • Deficiency or inhibitor of factor VII
    • Lupus anticoagulant (rarely)
  • Elevated PTT only
    • Heparin
    • Deficiencies of factor VIII, factor IX, factor XI, factor XII, or inhibitors
    • von Willebrand disease
    • Lupus anticoagulant
  • Elevated PT & PTT
    • Deficiences of prothrombin (factor II), factor V, factor X, fibrinogen
    • DIC

References