Clinical Approach to Hemostasis Flashcards
Disorders of Primary Hemostasis. Defining features
thrombocytopenia, platelet function defects, von willebrand disease, vascular disorders.
these cause disturbances in platelet plug formation.
• Defining features: – Present with mucocutaneous bleeding – Involve superficial tissues – Petechiae, purpura, epistaxis, mouth-related bleeding, menorrhagia – Immediate bleeding – May occur after minor trauma
Lab tests to order primary hemostasis
CBC
PBS
VWF studies
Bleeding time/
closure time– more sensitive than bleeding time.
Platelet aggregation studies to assess platelet function abnormalities (done through light transmission studies)
disorders of secondary hemostasis and defining features
Hemophilia A and B, coagulation factor deficiencies (could be caused by liver)
Defining features
– Hematomas, muscle bleeding, hemarthrosis, prolonged bleeding
– Involve deeper tissues : Look for significant hematomas. Look for joint DEFORMITIES which indicates previous bleeding events into joint spaces
– Bleeding is delayed and prolonged
– Bleeding is common after surgery
lab tests for secondary hemostasis
secondary hemostasis prevents fibrin clot formation. therefore, tests to assess the coagulation cascade is important
PTT/aPTT for intrinsic pathway (TENET)
PT/INR for extrinsic (factor 7-TF) pathway
- use both to assess common pathway (factor 10+ 5a+ 2(thrombin))
Thrombin time
measures conversion of fibrinogen to fibrin– final step oil clot formation
- irrespective of factor deficiencies in intrinsic/extrinsic cascade
- TT is affected by low fibrinogen levels, dysfunctional fibrinogen, or thrombin inhibitor.
T/F everyone should be screened for coagulation disorder
false. screen only if history is positive. Coagulation screening for disease state (e.g. liver
disease, malabsorption, malnutrition) – not
appropriate. No justification for routine coagulation screening on all hospital admissions.