Hemostasis Flashcards

1
Q

Intrinsic Path (measured): _ elements which activates…. to produce…

A

(PTT); exposed collagen +XII -> XI, IX-> X which activates thrombin to produce fibrin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Extrinsic pathway (measured): _elements -> _elements-> _product

A

(PT); tissue factor + VII -> activaed X -> fibrin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

_ is common to both extrinsic and intrinsic pathway

A

X

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

_ crosslinks _ to form ‘plug’

A

XIII crosslinks fibrin to form ‘plug’

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

… is best single test to evaluate synthetic function of the liver

A

PT

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Banked blood is low in _ which increases _

A

low in 2,3-DPG which increases Hgb affinity for o2 (left shift)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Cryo contains _ and _; used in _, _, _

A

fibrinogen and VWF-VIII; used in vWD, hemophilia A, and DIC if fibrinogen low

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Vit K inhibits:

A

II, VII, IX, X, protein C and protein S

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Protein C degrades…

A

active V and VIII; Protein S helps protein C

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

_ and _ are labile factors, low levels stored in blood

A

V and VIII

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

_ only factor no made in liver…. made by _

A

Factor VIII made by reticuloendothelial system

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Von Willebrands Disease:

PTT, BT, +/- ristocetin test?

A

Long PTT, long BT, +test

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Types of VWD with low amount:

Types of VWD with poor quality:

A

Type I and III have low amounts of vWF, these respond to ddAVP; type II is quality poor vWF

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

VwD inheritancy

A

autosomal dominant

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Rx for VWD: _, _, _

A

VIII, vWF or cryoprecipitate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

ddAVP causes _; also useful in _

A

release of VWF; useful in pts on ASA or w uremic plt

17
Q

Glanzman’s thrombasthenia:

defect. ..
effect. ..

A

plts have IIb/IIa receptor deficieny; decreases plt aggregation

18
Q

Brenard Soulier:

defect. ..
effect. ..

A

Ib deficiency; decre adherence to exposed collagen

19
Q

VII deficiency causes:

A

long PT, normal PTT

20
Q

Hemophilia A=
Inheritancy…
Preop replace…
PTT? PT? Newborn?

A

VIII deficiency; sex linked recessive, replace to 100% levels pre-op; long PTT, normal PT; newborn has VIII from mom, may not bleed at cicumcision

21
Q

Hemophilia B=
Inheritancy…
Preop replace…

A

IX deficiency= christmas disease; also sex-linked; achieve 50% levels pre-op

22
Q

Rx Hemophiliac joint

A

DO NOT ASPIRATE; ice ROM therapy, give factor VIII

23
Q

Lupus anticoagulant: pro/anti coagulant?

A

antiphospholipid antibodies; not necessarily with Luppus and generally pro-coagulant

24
Q

Dx Lupus anticoagulant:

A

long Russel viper venom time, long PTT, which does not correct by adding normal plasma

25
Q

Factor XII: activated by…. need for…

A

Hagemann factor; activated by cardiopulmonary bypass -> need for heparin

26
Q

Factor V Leiden:
Defect…
Effect…

A

Resistance to activated protein C; common cause of DVT

27
Q

Plasmin degrades _; inhibited by _

A

fibrinogen, inhibited by alpha-2-plasmin inhibitor

28
Q

Heparin binds/activates… and inactivates… PTT? How to counteract?

A

binds ATIII; inactivates factor 9-12; prolongs PTT; counteract with protamine

29
Q

Epsilon-ACA (Epsilon amino caproic acid); inhibits _; Rx for _

A

inhibits fibrinolysis; rx for overdose thrombolytics

30
Q

Best test to monitor thrombolysis

A

Thrombin

31
Q

DIC: platelets? PT? PTT? Fibrinogen? Fibrin Split products?

A

low platelets, prolonged PT/PTT, low fibrinogen, high fibrin split products

32
Q
HIT:
Defect...
Effect...
Use _ to anticoagulate
When to see?
Less often with?
A

‘white clot syndrome’; thrombocytopenia due to anti-platelet antibody causing plt aggregation; use dextran to anticoagulate; see after 5 days of heparin; less frequent with LMWH

33
Q

Prostacylcin
abv?
from?
Effect _, _, _

A

PGI2; from endothelium; decr plt aggregation, causes vasodilatation, bronchial relaxation

34
Q

Thromboxane:
from?
Effects?

A

from platelets; increase plt aggregation, VC, bronchial constriction

35
Q

Best preop test for pt on NSAIDS/ASA

A

Bleeding time