Topic 13: TEG Flashcards

1
Q

Clot strength - platelet to fibrin ratio

A
  • Platelets 80%-90%

* Fibrin 10%-20%

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

Tests that are Component Measurements of clots?

A
  • PT/INR:
  • PTT:
  • Fibrinogen concentration
  • Platelet Count
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

•PT/INR: measures what?

A

measures extrinsic clotting (VIIa, Xa, IIa)

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

•PTT:

A

measures intrinsic clotting (XIIa, Xia, IXa, IIa)

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

Test that Measures component interactions

A
  • TEG

* Shows net effect “whole picture” of hemostasis

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

TEG is ?

A
  • A whole blood hemostasis analyzer

* Point of care test

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

How does TEG work?

A
Cup oscillates
•Pin is attached to torsion wire
•Clot binds pin to cup
•Degree and magnitude of pin motion are functions of the clot kinetics and mechanical properties
•System generates a hemostasis profile
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

R

A

is the time of latency from the time that the blood was placed in the TEG until the fibrin formation

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

R

likely variable?

A

Reaction time (time to clot formation)
is the time of latency from the time that the blood was placed in the TEG until the fibrin formation
(coagulation factors)

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

alpha - α

likely variable?

A

Speed of fibrin accumulation
measure the rapidity of the fibrin build up and cross linking, that is, the speed of clot strengthening
(Fibrinogen)

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

K

likely variable?

A

Time elapsed until clot reaches a fixed strength
K time is a measure of the rapidity to reach a certain level of clot strength
(Fibrinogen)

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

MA

likely variable?

A

max amplitude, is a direct function of the max dynamic properties of fibrin and platelet bonding via GPIIb/GPIIIa and represents the ultimate strength of the fibrin clot
Highest vertical amplitude of TEG tracing
(Platelets)

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

CI

A

coagulation index is a linear combination of MA, K, Alpha, R

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

LY30

likely variable?

A

measures the rate of amplitude reduction every 30 minutes after MA. gives an indication of stability of the clot
% of amplitude reduction 30 minutes after its maximum
(Fibrinolysis)

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

LY30

likely variable?

A

measures the rate of amplitude reduction every 30 minutes after MA. gives an indication of stability of the clot
% of amplitude reduction 30 minutes after its maximum
(Fibrinolysis)

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

Standard (kaolin)

A

•Uses normal parameters

uses CI, MA, LY30, K, R alpha

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

Rapid TEG

A
  • Uses tissue factor in place of kaolin to speed up the reaction
  • R-value is replaced by TEG-ACT value
  • Other parameters the same
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Heparinase

A

•Used on bypass or post bypass alongside a standard TEG

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

Platelet Mapping

A
  • Determines to what degree platelet function is inhibited due to pharmacological inhibition of either the arachidonic acid (AA) or adenosine diphosphate (ADP) pathways
  • AA: Aspirin
  • ADP: Clopidogrel
  • Run alongside a standard TEG and a TEG with added AA or ADP.
  • Calculates platelet inhibition as a percentage
20
Q

Elongated R-Thrombin Formation Abnormalities:

Possible cause of imbalance:

A

•Slow enzymatic reaction

21
Q

Elongated R-Thrombin Formation Abnormalities:

Possible Etiologies

A
  • Factor deficiency/dysfunction

* Residual heparin

22
Q

Elongated R-Thrombin Formation Abnormalities:

Common Treatments:

A
  • FFP

* Protamine

23
Q

Low alpha angle - Fibrin formation

Possible cause of imbalance

A

slow rate of fibrin formation

24
Q

Low alpha angle - Fibrin formation

possible etiologies

A

Low fibrinogen levels or function
•Insufficient rate/amount of thrombin generation
•Platelet deficiency/dysfunction

25
Q

Low alpha angle - Fibrin formation

Common treatments

A
  • FFP

* Cryoprecipitate

26
Q

Low MA - possible causes?

A

Insufficient platelet-clot formation

27
Q

Low MA - possible etiologies

A

Poor platelet function
•Low platelet count
•Low fibrinogen levels or function

28
Q

Low MA - common treatments?

A

Platlets

29
Q

High MA - possible causes?

A

Excessive platelet activity

30
Q

High MA - possible etiologies?

A

Platelet

hypercoagulability

31
Q

High MA - common treatments

A

antiplatelet agents

32
Q

Platelet mapping measures what??

A

Measures the effect of antiplatelet agents on platelet function
•Measures the pt’s maximum platelet function as a
reference point
•Measures the percentage of inhibition relative to the patient’s reference point

33
Q

Platelet mapping – what drugs are monitored?

A

Antiplatelet Drugs
•ADP receptor inhibitors
•Examples: clopidogrel, ticlopidine

  • Arachidonic acid pathway inhibitors
  • Example: aspirin
  • GPIIb/IIIa inhibitors
  • Examples: abciximab, tirofiban, eptifibatide
34
Q

Why platelet mapping?

A

Individual response to antiplatelet drugs determines clinical outcome
•Knowing percent of platelet inhibition is insufficient to determine therapeutic efficacy
•Knowledge of maximum platelet function is also required as a reference point

35
Q

Rotational Elastometry (ROTEM)

A

Stationary cup, rotating spindle
•Clot impedes rotation of the pin
•Additional tests available

36
Q

R time between 7-10 min
clinical cause?
suggested treatment?

A

decrease clotting factors

1 FFP or 4 ml/kg

37
Q

R time between 11-14 min
clinical cause?
suggested treatment?

A

decrease clotting factors x2

2 FFP or 8 ml/kg

38
Q

R time greater than 14
clinical cause?
suggested treatment?

A

decrease clotting factors x3

4 FFP or 16 ml/kg

39
Q

MA between 49 - 54mm
clinical cause?
suggested treatment?

A

decrease platelet function

.3mcg/kg DDAVP

40
Q

MA between 41-58mm
clinical cause?
suggested treatment?

A

decrease platelet function

x5 platelet units

41
Q

MA 40 mm or less
clinical cause?
suggested treatment?

A

decrease platelet function x2

x10 platelets units

42
Q

LY30 7.5% or greater, CI less than 3.0
clinical cause?
suggested treatment?

A

primary fibrinolysis

antifibrinolytic

43
Q

LY30 7.5% or greater, CI greater than 3.0
clinical cause?
suggested treatment?

A

secondary fibrinolysis

anticoagulant of choice

44
Q

LY30 less than 7.5%, CI greater than 3.0
clinical cause?
suggested treatment?

A

prothrombotic state

anticoagulant of choice

45
Q

Antiplatelet Drugs
•ADP receptor inhibitors
•Examples:

A

Clopidogrel

Ticlopidine

46
Q

Antiplatelet Drugs
•Arachidonic acid pathway inhibitors

•examples

A

Aspirin

47
Q

Antiplatelet Drugs
•GPIIb/IIIa inhibitors

•Examples:

A

abciximab, tirofiban, eptifibatide