Module 2 Flashcards
What are the 3 steps of interpretation of a TEG?
MARLy
- Assess MA in CFF and CRT
- if low CFF MA (<15) replace fibrinogen with cryo or fibrinogen
- if normal CFF MA but low CRT MA (<52) give platelets once fibrinogen corrected) - Asses R in CK and CKH
- if both prolonged, heparin effect excluded, coagulation defect present
- if CKH R normal but CK R prolonged, heparin effect - Assess Ly30 on CRT
- if >2.2%, hyperfibrinolsis present, give TXA
Differentiate between types 2A, 2B, 2N and 2M vWD
2A: selective deficiency of HMW multimers
2B: increased affinity of vWF for platelet Gp1b (selective deficiency of HMW multimers)
2N: decreased affinity of vWF for FVIII
2M: dysfunctional vWF not associated with deficiency of HMW multimers
What are the initial tests for diagnosis of vWD?
vWF:Ag
- if undetectable type 3
vWF: RCo
>0.6 type 1
<0.6 type 2
vWF: CB
>0.6 type 1
<0.6 type 2
FVIII:C
- if only low FVIII:C, likely 2N or mild haemophilia A
Differentiate between TEG/ROTEM
- number of cups
- cup fixed or oscillating?
- electronic or optical detection?
TEG
- 1 cup
- fixed pin (oscillating cups)
- electronic detection
ROTEM
- 4 cups
- fixed cups (less distortion with vibration)
- optical detection
What are the indications to monitor DOACs?
- emergent/urgent surgery
- major bleeding
- dosing compliance or oOD
- acute thrombosis
- renal/liver failure
- drug interactions
What are the useful laboratory tests to monitor
- Rivaroaxaban
- apixaban
- endoxaban
- dabigatran
- fondaparinux
- argatroban
- bivalirudin
- Riv, apix, endo: direct fXa assay for individual agent
- dabigatran: TCT
- fondaparinux : anti-fXA
- argatroban/bival: APTT
What are the clinical and laboratory criteria for antiphospholipid syndrome?
What score do you require?
CLINICAL
- thrombosis
- recurrent pregnancy loss
- thrombocytopenia
LABORATORY
- lupus anticoagulant
- anti-cardiolipin antibody
- anti-B2GP1 antibodies
Need 2 or more lab and 2 or more clinical with repeated labs at 12 weeks
What is the confirmatory testing for lupus anticoagulant?
dRVTT
- LA screen: LA- sensitive regents, low quantities of PL, prolonges Ct
- LA confirm: LA- insensitive reagents, high wantities of PL, shortens CT
Screen:confirm ratio >1.2 indicative of LA
PNT
Hexagonal
Kaolin clotting time
Tissue thromboplastin inhibition test
Describe the pathophysiology of HITTs
PF4 found on endothelial cells and monocytes detaches in presence of heparin and formsH-PF4 commplexes
Antibodies are formed to these antigen sites
Antibodies bind and activate platelets leading to platelet activation aggregation, thrombosis and a positive feedback loop generating more PF4
What are the 4 Ts used to diagnose HITTS and what scores are required?
Thrombocytopenia
Timing: 1 point for days 5-10 fall but unclear, 2 points for clear with recent exposure
Thrombosis: 1 point for progressive/recurrent or non-necrotising skin lesions, 2 for new thrombosis or skin necrosis
Other: 1 for possible, 2 for none
0-3 low
4-5 intermediate
6-8 is high
What are the key lab investigations for diagnosis of HITTS?
Screening: Rapid antibody detection or immunoassay
Diagnostic: serotonin release assay gold standard, Heparin induced platelet aggregation, electrode aggregometry, Light transmission aggregometry