blood & Videos Flashcards

(58 cards)

1
Q

hemostasis -

A

a term means to stop bleeding -prevents exsanguination following injury, trauma and or surgery

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

zymogens

A

inactive enzymatic precursors of most coagulation factors

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

proteases

A

catalyst transforming inactive into an active state

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

extrinsic factor

A

7

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

intrinsic factor

A

9, 11, 12, (8)

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

common pathway factor

A

10, 2, 13

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

pathway for pt

A

extrinsic

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

pathway for ptt

A

intrinsic

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

what does the post op anabolic state do to coagulation factors

A

increases hemostatic factors for several days

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

factor 1

A

fibrinogen

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

factor 2

A

prothrombin

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

factor 3

A

thromboplastin /tissue factor

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

factor Iv

A

calcium

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

factor V

A

labile factor/proccelerin

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

factor VII

A

SPCA- serum prothrombin converting accelerator

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

factor VIII

A

anti hemophilic a factor

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

factor IX

A

christmas factor

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

factor X

A

stuart factor

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

factor XI

A

plasma thrombplastin antecedent

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

factor XII

A

hageman factor

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Factor XIII

A

fibrin stabilizing factor

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

because of loss of vascular endothelial function and other prohemostatis changes, venous and arterial thromboembolic events -when does this occur

A

increases with age.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

antiphospholipid syndrome is caused by

A

lupus anticoagulant (phoslipid binding antibody)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

antiphospholipid syndrome- cause by lupus anticoagulant will present with

A

prolonged prothrombin times and partial thromboplastin times

BUT-they are hyper coagulable.

25
what is the most common cause of thrombocytopenia in the perioperative setting
dilutional effect following volume resuscitation
26
treatment for DIC
antibiotics removed underlying problem instituting anticoagulation *support organs
27
at the center of hemostasis is the ability to generate
thrombin
28
thrombin plays a role in activation of additional
coagulation factors
29
What factor activates Factor 10?
factor 9a
30
the first factor in the common pathway
factor 10
31
factor 7 converts to 7a through
Tissue factor (factor 3)
32
10a acts as a protease and converts
``` factor 2 (prothrombin) to factor 2a (thrombin) ```
33
Thrombin converts
fibrinogen to fibrin (monomer)
34
Fibrin clot is eventually broken down by
fibrinolytic
35
plasminogen --> plasmin is the ultimate fibrinolytic and
breaks down the fibrin clot
36
Fibrinolytic therapy vs anticoagulation
fibrinolytics: activate plasmin to breakdown clots anticoagulation: prevent fibrin clots from forming
37
Hemophilia A hallmark lab values
normal BT | Normal PLT count
38
In Hemophilia A, factor X can't be activated as well. this results in
fibrin polymer meshwork to not form
39
Hemophilia B is a deficiency of which factor? it's also known as?
Christmas Tree disease
40
Protein C inactivates
Factors Va and VIIIa (58)
41
Coumadin binds to
vitamin K
42
Protein S makes
Protein C (breaks down 5a and 8a) *require Vit K to work
43
PT and PTT do not measure what factor?
XIII (13)
44
Heparin principally acts on
Antithrombin (AT)
45
Heparin makes AT do what?
"it's on steroids" heparin makes AT work really well
46
Heparin's impact on AT inactivates
factors II, X -- the common pathway blocks coagulation
47
LMWH are short chained
polysaccharides
48
Unfractionated Heparin need to monitor
PTT
49
Heparin Induced Thrombocytopenia
- decreased PLT count caused by heparin - hypercoagulability - IgG antibodies against heparin bind to Factor IV (calcium) - antibodies+heprin/PLT factor IV complex will activate PLT and form clots
50
PLT: decreased BT: increased PT: normal PTT: normal What is this disorder?
Thrombocytopenia
51
PLT: Normal BT: increased PT: normal PTT: increased What is this disorder?
von Willebrand Disease
52
PLT: normal BT: normal PT: normal PTT: increased What is this disorder?
Hemophilia A
53
PLT: decreased BT: increased PT: increased PTT: increased What is this disorder?
DIC
54
PLT: normal BT: increased PT: increased PTT: increased What is this disorder?
primary fibrinolysis
55
PLT: normal BT: increased PT: normal PTT: normal What is this disorder?
Aspirin or NSAIDs
56
PLT: normal BT: normal PT: increased PTT: increased What is this disorder?
Warfarin or Heparin
57
ABL =
[EBV x (Start Hct – Target Hct)] / Start Hct
58
Sponge (4x4) = | lap sponge =
Sponge (4x4) = 10ml | lap sponge = 100-150ml