Coagulation panel Flashcards

(33 cards)

1
Q

aterial thrombosis

A
  • platelet rich + white.
  • caused by atherosclerosis and endothelium damage
  • adheres to vessel walls
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2
Q

venous thrombosis

A
  • rbc rich + red
  • loosely attached
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3
Q

what’s added to tube when measuring coagulation factors to stop clotting

A

citrate

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4
Q

what does PT measure

A

time taken to clot in extrinsic and common pathways

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5
Q

what does APTT measure

A

time taken to clot in intrinsic and common pathways

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6
Q

what does INR measure

A

ratio of normal PT compared to patient PT therefore ideal INR is ~1.
only technically valid for warfarin.

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7
Q

what triggers intrinsic pathway

A

contact factor

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8
Q

what triggers extrinsic pathway

A

tissue factor

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9
Q

what is a DOAC

A

direct acting oral anticoagulant

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10
Q

which DOACs inhibit factor X

A

rivaroXaban, edoXaban, apiXaban

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11
Q

which DOAC inhibits factor II

A

Dabigatran (anti-thrombin)

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12
Q

How do DOACs affect coag panel tests

A

variable non-linear impact on PT and APTT

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13
Q

what are DOACs used for

A

stroke prevention, DVT, pulmonary embolism

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14
Q

what cofactor does synthesis of IX, X, II, and VII require

A

vitamin K

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15
Q

what is warfarin

A

a vitamin K antagonist therefore anticoagulant

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16
Q

what coag panel tests does warfarin affect

A

prolongs PT and APTT
PT is particularly sensitive to it.
INR used to adjust dose

17
Q

what are heparins

A

sulphated glycosaminoglycans.

18
Q

how do heparins inhibit coagulation

A
  • indirectly by increasing anticoagulant power of antithrombin
  • mainly affects factors IIa and Xa
19
Q

how is unfractionated heparin delivered

A

intravenously with loading dose before continuous infusion.
needs careful monitoring
binds to antithrombin and thrombin

20
Q

how is low molecular weight heparin delivered

A

subcut injection
only binds to antithrombin which acts on factor Xa

21
Q

how does heparin affect coag panel test

22
Q

what do thrombolytic drugs target

A

plasminogen e.g. tPA

23
Q

primary prevention using anti platelets

A

if high cardiovascular risk score

24
Q

secondary prevention using anti platelets

A

after MI, stroke, stent, PVD

25
2 examples of anti-platelets
aspirin and clopidogrel
26
Haemophilia A
makes no or little factor VIII increases APTT
27
Haemophilia B
makes no or little factor IX increases APTT
28
what does Von Willebrand factor do
- binds platelets and exposed endothelium. - carrier for FVIII
29
Quantitative Von Willebrand disease
low levels of Von Willebrand factor
30
qualitative Von Willebrand disease
abnormal function of Von Willebrand factor
31
how might VWD be detected on coag panel
prolonged APTT as less FVIII
32
symptoms of VWD
easy bruising, mucosal bleeding
33
disseminated intravascular coagulopathy (DIC)
- normal haemostasis not regulated properly - coagulation activated and fibrin deposit so thrombi form - causes clotting factors and platelets to run out so then start bleeding a lot.