heme externship - coag 2.3-2.4 Flashcards
the APTT is sensitive to a deficeincy of which clotting factor
A. FVII
B. FX
C. PF3
D. calcium
B. FX
which test result would be normal in a patient with dysfibrinogenemia
A. TT
B. APTT
C. PT
D. immunologic fibrinogen level
D. immunologic fibrinogen
- measures total fibrinogen
a patient with prolonged PT is given intravenous vitamin K. OT is corrected to normal after 24 hours. which clinical condition most likely caused these results
A. nectortic liver disease
B. FX deficiency
C. fibrinogen deficiency
D. obstructive jaundice
B. FX deficiency
which factor deficiency is associated with prolonged PT and APTT
A. FX
B. FVIII
C. FIX
D. FXI
A. FX
prolonged APTT is corrected with FVIII deficient plasma but not with FIX deficient plasma. which factor is deficient
A. FV
B. FVIII
C. FIX
D. FX
C. FIX
which of the following is a characteristic of classic hemophilia A
A. abnormal PLT aggregation
B. autosomal recessive inheritance
C. mild to severe bleeding episodes
D. prolonged PT
C. mild to severe bleeding episodes
- FVIII deficiency
which disorder may be indicated with the following results:
- PT: prolonged
- APTT: prolonged
- PLT count: decreased
A. FVIII deficiency
B. vWF disease
C. DIC
D. FIX deficiency
C. DIC
which of the following is a predisposing condition for the development of DIC
A. adenocarcinoma
B. ITP
C. PTP
D. HIT
A. adenocarcinoma
- releases thromboplastic substances
FXII deficiency is associated with:
A. bleeding
B. epistaxis
C. decreased risk of thrombosis
D. increased risk of thrombosis
D. increased risk of thrombosis
the following results were obtained on a patient:
- PLT count and function: normal
- PT: normal
- APTT: prolonged
which of the following disorders is most consistent with these results
A. hemophilia A
B. bernard-soulier syndrome
C. vWF disease
D. glanzmanns thrombathenia
A. hemophilia A
- FVIII deficiency
the following lab results were obtained from a 40 year old woman:
- PT: 20 seconds
- APTT: 50 seconds
- TT: 18 seconds
what is the most probably diagnosis
A. FVII deficiency
B. FVIII deficiency
C. FX deficiency
D. hypofibrinogenemia
D. hypofibrinogenemia
- PT RR: 13-16
- TT RR; 14-20 (harr says lower)
- CTT RR: 16-22
- APTT RR: 26-36
when performing a FVIII activity assay, a patients plasma is mixed with
A. normal patient plasma
B. FVIII deficient plasma
C. plasma with high concentration of FVIII
D. normal control plasma
B. FVIII deficient plasma
the most suitable product for treatment of a FVIII deficiency is
A. FFP
B. FVIII concentrate
C. prothromin complex concentrate
D. FV Leiden
B. FVIII concentrate
- if the deficiency is known it is best to treat it ith its corresponding concentrate
- if unknown then FFP is used
which of the following is associated with an abnormal PLT aggregation test result
A. FVIII deficient
B. FVIII inhibitor
C. lupus anticoagulant
D. afibrinogenemia
D. afibrinogenamia
which of the following disorders is indicated by the results:
- PT: Normal
- APTT: prolonged
- PLT count: normal
- PLT aggregation to ristocetin: abnormal
A. FVIII deficiency
B. DIC
C. vWF disease
D. FIX deficiency
C. vWF disease
- missing vWF = missing FVIII = prolonged APTT
- abnoraml ristocetin = no vWF agglutination
which results are associated with hemophilia A
A. prolonged APTT, normal PT
B. prolonged PT and PATT
C. prolonged PT and normal APTT
D. normal PT and APTT
A. prolonged APTT, normal PT
fibrin monomers are increased in which of the following conditions
A. primary fibrinolysis
B. DIC
C. FVIII deficiency
D. fibrinogen deficiency
B. DIC
- nor primary fibrinogenolysis because that would be fibrinogen monomers, fibrin monomers are formed after coagulation
which of the following is associated with multiple factor deficiencies
A. an inherited disorder of coagulation
B. severe liver disease
C. dysfinrinogenemia
D. lupus anticoagulant
B. severe liver disease
- most coag factors are made in the liver so no liver no coag factors
normal PT and APTT results in a patient with poor wound healing may be associated with
A. FVII def
B. FCIII def
C. FXII def
D. FXIII def
D. FXIII def
- normal in vitro but no clot stabilization in the body
Fletcher factor (prekallikrein) deficiency may be associated with
A. bleeding
B, thrombosis
C. thrombocytopenia
D. thromobocytosis
B. thrombosis
- part of clot degredation in plasminogen activation
one of the complications associated with severe hemophilia A is
A. hemarthrosis
B. mucous membrane bleeding
C. mild bleeding during surgery
D. immune mediated thrombocytopenia
A. hemarthrosis
- bleeding in the joints
the most common subtype of classic vWF disease is
A. type 1
B. type 2a
C. type 2b
D. type 3
A. type 1
- universal decrease of all monomers
prolonged APTT and PT are corrected when mied with normal plasma. which factor is most likely deficient
A. FVIII
B. FV
C. FXI
D. FIX
B. FV
- common pathway
which characteristic describes antithrombin (AT)
A. synthesized by megakaryocytes
B. activated by protein C
C. cofactor of heparin
D. pathological inhibitor of coagulation
C. cofactor for heparin
which lab test is affected by heparin therapy
A. thrombin time
B. fibrinogen assay
C, protein C assay
D. protein S assay
A. thrombin time
abnormal APTT caused by a pathological circulating anticoagulant is:
A. corrected with FVIII deficient plasma
B. correct with FIX deficient plasma
C. corrected with normal plasma
D. not corrected with normal plasma
D. not corrected with normal plasma