Day 10 - HemOnc2 Quiz Flashcards
TTP Pentad
Thrombocytopenia, hemolytic anemia, renal failure => uremia (HUS); fever, neuro sx (AMS, seizures, coma)
Most common mutation in white pts predisposing to venous thrombosis
Factor V leiden
Drug mechanism: Streptokinase
thrombolytic (like tPA), cleaves fibrin clots
Drug mechanism: ASA
Inhibits cyclooxygenase, inhibiting platelet aggregation
Drug mechanism: Clopidogrel
ADP receptor blocker
Drug mechanism: Abciximab
GpIIbIIIa inhibitor (like Tirofaban)
Drug mechanism: Ticlopidine
ADP receptor blocker (like clopidogrel)
Drug mechanism: Enoxaparin
LMWH, inhibits factor Xa
Drug mechanism: Eptefibitide
GIIbIIIa inhibitor
Lab test(s) used to monitor: (1) warfarin (2) heparin (3) LMWH
(1) INR (2) PTT (3) Anti-Factor Xa (if needed to be monitored)
Tx vWD
Desmopressin; Severe bleeding - cryoprecipitate or Factor VIII; Menorrhagia - OCPs; Avoid ASA and other platelet inhibitors
Lab changes: HUS/TTP
Low platelet count, Elevated bleeding time, Normal PT/PTT
Lab changes: Hemophilia A/B
Elevated PTT, Normal PT, platelet count and bleeding time
Lab changes: vWD
Normal platelet count, Elevated bleeding time, Normal PT, Elevated PTT
Lab changes: DIC
Platelet count low, Bleeding time high, PT/PTT Elevated