Coagulation Flashcards

1
Q

Method of coag

A

endothelial damage exposes procoag factors -> haemostatic response -> plt aggregation

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2
Q

What coag factors are prod by endothelial cells

A

PGI2, VWF, plasminogen activators, thrombomodulin

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3
Q

platelet adhesion

A
direct = Glp1a
indirect = Glp1b and vwf
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4
Q

how to platelets attach to each other

A

Glp2b and Glp3a (fibronogen R)

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5
Q

what does plt adhesion cause

A

release of ADP and thromboxane A2 (-> aggregation)

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6
Q

arachidonic acid -> ____ (+via)

A

-> endoperoxidases (via COX)

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7
Q

what are endoperoxidases conv to

A
  • > thromboxane A2 (stim agg)

- > PGI2 (inhib agg)

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8
Q

aspirin vs NSAIDS

A

aspirin - irrev inhib COX

NSAIDs - rev

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9
Q

actions of thrombin

A

activates F7, F8, F5, plt, F11, F13 (-> propogation)

catylises fibronogen -> fibrin

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10
Q

why is vit K important in coag

A

req as co-enz for lots of liver prod factors (2,7,9,10)

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11
Q

3 physiological anticoag

A

TFPI - stop F7-F7a (no initiation)
Prot c/Prot s - bind to thrombomodulin - stop 8->8a and 5->5a
antithrombin - stop prothrombin->thrombin and 10->10a

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12
Q

sympto of platelet disorders

A

petechiae, purpura, sml bruises, no haemoarthrosis

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13
Q

sympto of coag F disorders

A

bleeding in soft tissues (joints/muscles), large bruises

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14
Q

inheritance of haemophilia

A

X linked congen def of F8 (A) or F9 (B)

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15
Q

signs / sympto haemophilia

A

long APTT, normal PT, haemoarthrosis, soft tissue haematomas

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16
Q

inheritance of VWD

A
T1/2 = auto dom
T3 = auto rec
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17
Q

Signs sympto of VWD

A

mucocutaneous bleeding, dec plt count, inc bleeding time, inc APTT, normal PT

18
Q

types of VWD

A

T1 - patrial
T2 - qualitative
T3 - total

19
Q

causes of vit K def (5)

A
malnut
malabs
biliary obs
warfarin (most common)
antibiotics
20
Q

causes of DIC

A

activation of coag + fibrinolysis by sepsis/trauma/obstetric comp

21
Q

findings in DIC

A

long APTT/TT/PT, dec fibrinogen/platelets

22
Q

Tx for VWD

A

desmopressin

23
Q

What factors is Vit K needed for

A

2,7,9,10 (buses to south ken)

24
Q

what factor goes first in vit K def

A

7

25
Q

important DDX in vit K def

A
liver disease ( would -> dec plt count) 
scurvy ( -> corkscrew hair)
26
Q

most common prothrombotic disorder

A

F5 lieden

27
Q

signature of F5 lieden

A

thrombosis in weird places

28
Q

inheritance of prot c/s def

A

auto dom

29
Q

what is prot c/s associated with

A

warfarin induced skin necrosis

30
Q

how would you give heparin

A
unfractionated = IV 
LMWH = SC
31
Q

monitoring for heparin

A

unfrac - (variable kinetics) monitor APTT or anti-Xa

LMWH - none

32
Q

safest anticoag to use in preg

A

LMWH

33
Q

how would you give DOAC

A

oral

34
Q

monitoring for DOAC

A

none (short half life)

35
Q

DOAC in preg?

A

no - cross placenta

36
Q

3 doac that are anti X-a

A

rivaroxaban, apixaban, edoxaban

37
Q

1 doac that is anti II-a

A

dibagatran

38
Q

what falls first in warfarin

A

prot c/s - is procoag initially

39
Q

what pro-coag factor falls first in warfarin

A

7

40
Q

what factor falls lats in warfarin

A

11

41
Q

warfarin in preg?

A

never - teratogenic

42
Q

monitoring in warfarin

A

monitor INR daily (aim for 2-3)

if 5-9 - omit dose and give oral vit K