Lecture 9 - Coagulation testing Flashcards

1
Q

what sample is used for most coagulation testing

A

PLASMA (use a citrate/blue tube)

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2
Q

why not use serum

A

it clots and lacks factors needed for testing

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3
Q

4 venipuncture sample tips

A
  1. use plastic syringe and tube
  2. fresh, clean stick
  3. do not collect from catheter
  4. properly fill the tube
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4
Q

__ inhibits coagulation by binding calcium

A

sodium citrate

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5
Q

ratio of citrate to blood MUST be __ why need to fill it appropriately

A

1:9

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6
Q

Analysis must be preformed ASAP or

A

plasma should be frozen within 30mins

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7
Q

After centrifugation what is present in citrated plasma

A

only coagulation factors and other blood chemicals

(NO WBC, RBC, Platelets, or Ca!)

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8
Q

7 tests for coagulation/hemostatic function

A
  1. PT
  2. PTT
  3. ACT
  4. Fibrinogen concentration and TT
  5. FDPs
  6. D-dimers
  7. thromboelastography
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9
Q

__ coagulation model is not what happens in the body but what happens in the tube, important for understanding tests

A

classic cascade

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10
Q

cats, manatees, dolphins and other exotics lack __

A

factor 12

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11
Q

__ tests the extrinsic (and common) pathway

A

PT (prothrombin time or one stage prothrombin time) measures time for clot to form when tissue thromboplastin is added = “extrinsic”

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12
Q

How does PT test the extrinsic pathway

A

measures time for fibrin clot to form in citrated plasma after adding tissue factor (thromboplastin), Ca, and substitute for platelet = “extrinsic” bc adding things

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13
Q

a __ % deficiency is required before prolognation of PT and PTT

A

70%

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14
Q

prolonged PT means there is inhibition or deficiency of

A

factor 7, tissue factor or the common pathway factors

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15
Q

what factors are vitamin K dependent coagulation factors

A

2, 7, 9, 10

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16
Q

PT can be used to monitor __ therapy

A

warfarin

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17
Q

PT is the best test for __

A

vitamin K antagonism or deficiency

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18
Q

__ and __ test the intrinsic (and common) pathway

A

PTT (activated Partial Thromboplastin Time) and ACT

19
Q

Which test does NOT have tissue factor/thromboplastin added to tube?

A

PTT (why it’s “intrinsic”). only add things already in the body like contact activator, Ca, and platelet substitute

20
Q

PTT and ACT can be used to monitor __ therapy

21
Q

artificially prolonged test times can be caused by

A
  1. delayed testing
  2. warm sample
  3. low plasma citrate ratio (inappropriate filled tube) = erythrocytosis
22
Q

__ test uses patient’s own clotting factors, Ca and platelet’s, it can be done in the clinic for this reason!

23
Q

ACT measures time for fibrin clot to form in __ sample using special tube and patient’s own factors

A

WHOLE BLOOD (PT and PTT tests are run using citrated plasma)

24
Q

ACT stands for

A

activated clotting/coagulation time

25
ACT must be __% deficient before prolongation is detected
95% (compared to 70% for PT and PTT) - Not the best test for this reason, but better than nothing
26
severe __ can prolong ACT results
thrombocytopenia
27
ACT sample needs to be ran at __ temperature
body T (37C)
28
ACT and PTT test the same thing but the __ are different
prolongation detections
29
PT stands for
prothrombin time
30
PTT stands for
activated partial thromboplastin time
31
ACT stands for
activated clotting time
32
TT stands for
thrombin time (qualitative and quantitative fibriongen defects)
33
fibrinogen estimated by heat ppt is better at detecting
elevations than decreases decrease = conversion of fibrinogen to fibrin DIC Increase = inflammation
34
Does fibrinogen increase or decrease with DIC
Decrease
35
fibrinogen estimate heat ppt test does NOT detect __ fibrinogen activity, it only estimates fibrinogen quantity
defective
36
__ is a more specific measurement of fibrinogen quantity and activity (not readily available, also don't usually need these specific measurements)
TT (thrombin time) and Thromboelastography
37
role of plasmin in fibrinolysis
breaks fibrinogen/fibrin down into FDPs and D-dimers
38
What are FDPs (or FSPs)
fibrinogen and fibrin degradation products
39
FDPs are formed from Plasmin degradation of
fibrinogen, fibrin monomers, and crosslinked fibrin
40
__ are formed by plasmin degradation of crosslinked fibrin
D-dimers (and FDPs)
41
increased concentration of __ and __ INHIBITS coagulation and promotes bleeding
FDPs and D-dimers
42
__ is increase of FDPs only (seen in envenomations, exess TPA release during shock, heatstroke, sx trauma)
fibrinogenolysis (promotes bleeding)
43
__ from DIC, sepsis/inflammation, internal hemorrhage, or thromboembolic dz will see BOTH D-dimers and FDPs
increased fibrinolysis