Coagulation Flashcards

1
Q

3 steps of hemostasis

A

vasospasm
platelet plug fomation
coagulation

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2
Q

hemostasis

A

the ability to minimize blood loss

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3
Q

vasospasm

A

vasoconstriction

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4
Q

4 steps of platelet plug formation

A
  1. adhesion
  2. platelet activation
  3. platelet aggregation
  4. platelet plut
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5
Q

vonWillebrand factor (vWH)

A

holds platelets up to the exposed collagen

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6
Q

platelet activation

A

platelets release chemical messages to get more platelets to come (ADP, seratonin, thromboxane, A2)

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7
Q

platelet aggregation

A

a bunch of platelets come together to plug up the exposed area

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8
Q

prostacyclin

A

secreted by neighboring, healthy cells so that platelets only aggregate in the correct area

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9
Q

factor XII

A

activated when surface contact-turns into activated 12a

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10
Q

what is thrombin’s key function?

A

turn fibrinogen into fibrin (active form)

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11
Q

fibrinolysis

A

breakdown of a clot and resorbtion of the clot

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12
Q

plasmin

A

enzyme responsible for the breakdown of fibrin

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13
Q

normal platelet count

A

150,000-450,000/ uL

-not a measure of function

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14
Q

why is the patient bleeding?

A

platelet?

coagulation?

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15
Q

platelet bleeding problems may be seen with

A

petechiae, ecchymosis or purpura

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16
Q

thrombocytopenia

A

low platelet count

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17
Q

reasons why platelets may not be working

A

aspirin
uremia
genetic disorders (rare)
vWF (can’t bind without it)

18
Q

bleeding test

A

BT (higher it is, the longer you bleed)

-not used anymore

19
Q

normal range PT (prothrombin time)

A

13-17 seconds

20
Q

what does the PT measure?

A

extrinsic and common pathways
(5, 7, 10, 2 and 1)
-INR (intl normalized ratio)
-used to monitor coumadin

21
Q

increased PT time values may indicate

A

vitamin K deficiency and liver disease

22
Q

vitamin K deficiency can be caused by

A

bile duct obstruction

malabsorption

23
Q

liver disease affects coagulation in that

A

vitamin K is used by the liver to make the clotting factors and bile salts are also used and formed in the liver

24
Q

normal values for the aPPT

A

25-36 seconds

25
what does the aPPT measure?
intrinsic and common pathway (12, 11, 9, 8, 10, 5, 2, 1) -used to monitor heparin therapy
26
what conditions would cause a prolonged aPPT?
``` hemophilia A (missing factor 8) hemophilia B (missing factor 9) biliary obstruction (no vitamin K absorbed) hepatocellular diseases ```
27
normal ranges for fibrinogen
150-350 mg/dl
28
what is fibrinogen used for?
diagnose fibrinogen disorders or inhibitors of thrombin | -also to diagnose problems with fibrinolysis
29
when might fibrinogen be increased?
tissue inflammation
30
normal ranges of TT (thrombin time)
15-18 seconds | -measures common pathway
31
tissue factor pathway inhibitor
acts on the common pathway to control the clot
32
bleeding differential diagnosis
``` CALFDIPS cirrhosis and coumadin aspirin leukemia factor definciency (hemophilia) disseminated intravascular coagulopathy idopathic thrombocytopenic purpura (ITP) platelet deficiency or dysfunction scurvy-vitamin C deficiency ```
33
vonWillebrands disease
most common inherited congenital bleeding disorder | -clinical presentation is bleeding (nasal, sinus, vaginal, GI, deep tissue bleeding)
34
what other factor is related to the vWF?
factor VIII
35
how is DDAVP used?
treat VWD (stimulates release vWF)
36
hemathrosis
main symptom of hemophilia | -hematoma of the joints
37
expected lab results for hemophilia
aPPT will be high | PT will be low
38
FDP
fibrinogen degradation products
39
how does aspirin prevent clotting?
kills platelet function for the life of the platelet
40
how do NSAIDS prevent clotting?
deactivate platelet, but function returns w/in 24 hours
41
what is the main symptom of hemophilia a or b?
hemarthrosis
42
what are the causes of hypercoagulability?
too many platelets vascular injury clotting factors not working properly (anticlotting factors) stasis and surgery