Coagulation / Bleeding Disorders Flashcards

1
Q

What type of vessels use primary hemostasis the most?

A

arteries

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2
Q

What type of vessels use secondary hemostasis the most?

A

veins

i.e: DVT

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3
Q

Platelet function assay

A

another name for closure time

measures how long for primary hemostasis to form platelet plug in test tube

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4
Q

vWF antigen vs. activity

A

antigen is more specific

low vWF antigen and activity can mean vWD

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5
Q

Ristocetin co-factor

A

another term for vWF activity

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6
Q

Type I vWD

A

reduced vWF number but it functions correctly overall

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7
Q

thrombocytopenia

A

low platelet count

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8
Q

What is common signs of thrombocytopenia?

A

purpura and petechiae

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9
Q

what is there a risk of with Thrombocytopenia?

A

spontaneous bleeding due to lack of platelets

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10
Q

high risk of bleeding thrombocytopenia values

A

<10,000

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11
Q

low risk of bleeding thrombocytopenia values

A

<20,000

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12
Q

Immune Thrombocytopenic Purpura

A

viral infection causes an immune response against platelets

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13
Q

Immune Thrombocytopenic Purpura treatment

A

platelet transfusion will not work as antibodies will just degrade them

need immunosuppression or splenectomy

problem with platelets = primary hemostasis problem

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14
Q

What conditions cause thrombocytopenia by increased consumption of platelets?

A

DIC, HUS, Heparin Induced Thrombocytopenia

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15
Q

What specifically does aspirin affect?

A

aspirin = antiplatelet

prevents step 2 of primary hemostasis (no degranulation of platelets)

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16
Q

COX1 and platelets

A

aspirin activates COX1 which releases prostaglandins

prostaglandins prevent platelet granulation release

17
Q

what type of bleeding indicates primary hemostasis?

A

mucosal

18
Q

what type of bleeding indicates secondary hemostasis?

A

deep / joint

19
Q

for secondary hemolysis, what labs are checked next?

A

PT and PTT

then mixing studies

20
Q

why are platelets seen more in the arteries?

A

platelets are more stable in that higher pressure system

21
Q

what is the primary tests for primary hemostasis?

A

vWF and ITP

*looking for a platelet problem

22
Q

what are the vitamin K dependent factors?

A

2, 7, 9, 10

23
Q

What 2 things should you think about if both PTT and PT are delayed?

A

fibrinogen or vitamin K def.

common pathway problem

24
Q

hemarthrosis

A

swollen, hot joint

common in hemophilia patients

25
Q

ITP stands for …

A

immune thrombocytopenia purpura

26
Q

difference and similaries in vWD and ITP

A

both: affect the primary hemostasis pathway

difference: ITP is more diffuse. Platelets are also normal in vWD but low in ITP

27
Q

platelet count in vWD

A

normal!

have a deficiency of vWF, not platelets

28
Q

What do you treat vWD with?

A

DDAVP

releases more vWF from endothelial cells

could also give recombinant vWF infusions

29
Q

What do you treat non-immune thromocytopenia with?

A

platelet transfusion

30
Q

What do you treat secondary hemostasis disorders with?

A

either recombinant factors or fibrinogen transfusion

31
Q

What 4 conditions can lead to an unprovoked clot?

A

Factor V Leiden

Prothrombin

Protein C/S not working

Antithrombin III not working

32
Q

What can an EKG show in setting of PE?

A

a right heart strain due to blockage of the pulmonary vein putting more pressure on the heart

32
Q

What is most definitive way to look for PE?

A

CTA of chest

33
Q

antiplatelet drugs

A

aspirin and clopidigrel

34
Q

anticoagulation drugs

A

warfarin, heparin, NOAC

35
Q

how does clopidigrel work?

A

binds to the GPIIb/GPIIIa complex through P2Y12

36
Q

why don’t we give thrombolytics, like tPA more?

A

they have high associated bleeding risk

use for acute PE

37
Q

why don’t we need to check PT/PTT for coagulation disorders?

A

those tests look at bleeding disorders

38
Q
A