4.2 - Secondary hemostasis and related disorders Flashcards

1
Q

where does the calcium required for coagulation cascade activation come from?

A

platelet dense granules

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2
Q

hemophilia A is due to a defective in factor ___ and the inheritance is ____

A

8, XR

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3
Q

hemophilia B is due to a defective factor ___ and the inheritance is ____

A

9, XR

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4
Q

if PTT does not correct upon mixing normal plasma with patient’s serum (mixing study), what should you consider?

A

coagulation factor inhibitor - acquired autoantibody against a coagulation factor (usually 8)

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5
Q

how can coagulation factor inhibitor be differentiated from hemophilia A?

A

mixing study - PTT DOES correct in hemophilia A, when mixing normal plasma with patient’s serum

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6
Q

what are the lab findings in vWF disease?

  • bleeding time
  • PTT
  • ristocetin
A
  • increased bleeding
  • increased PTT
  • abnormal ristocetin
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7
Q

what is the treatment for vWF disease? why?

A
  • desmopression, which increases vWF release from weibel palade bodies of endothelial cells (vWF helps stabilize factor 8)
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8
Q

what is the relationship of vWF to factor 8?

A

vWF helps stabilize factor 8

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9
Q

vitamin K is activated by _________ in the liver

A

epoxide reductase

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10
Q

activated vitamin K carboxylates which factors?

A

2, 7, 9, 10, C, S

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11
Q

the effect of liver failure on coagulation is followed via what test?

A

PT

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