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Table 2 Indications and limitations of tests available in the hemostasis laboratory

From: Management of the thrombotic risk associated with COVID-19: guidance for the hemostasis laboratory

 

Main Limitations

Indications in COVID-19

Evaluation of the thrombotic risk

Screening of thromboembolic events

Prognosis: disease severity

Diagnosis of DIC

Detection of HIT

Monitoring of unfractionated heparin

Platelet count

Many causes of thrombocytopenia in the critically ill patient

  

X

X

X

 

APTT

Major influence of preanalytical step

    

X (*)

X

Differences of APTT reagents in their sensitivity to unfractionated heparin, lupus anticoagulant and inflammatory syndrome

Prothrombin Time

Influence of the preanalytical step

   

X

  

Influence of fibrinogen level

Fibrinogen (Clauss)

Lack of sensitivity for the diagnosis of DIC (mostly in infectious/inflammatory setting)

X

 

X

X

  

Possibility of interference of direct thrombin inhibitors with some reagents

D-dimers

Decreased analytical performances in high D-dimers values

X

X

X

X

  

Production dependent on the fibrinolytic activity

Cut-offs non commutable between reagents

Soluble fibrin complexes (AKA ‘Fibrin monomers’)

Preliminary validation only

 

X

 

X

  

Not evaluated in COVID-19

Cut-offs non commutable between the reagents

Fibrinolysis capacity tests

Fibrinolysis is assessed in non-physiological conditions

X

 

X

   

Large array of methods

Not evaluated in COVID-19

Anti-Xa activity

Inter-reagent variability

     

X

Influence of presence/absence of exogenous AT in the reagent

Expensive

Only available 24 h a day 7 days a week in a fraction centers

Viscoelastic tests

Not evaluated in COVID-19

X

 

X

  

X

Lack of standardization between instruments and centers

Expensive

Thrombin generation assays

Not evaluated in COVID-19

X

     

High sensitivity to heparins

Limited availability in clinical practice

Expensive

  1. (*) Heparin resistance can be due to HIT.
  2. Note: the assessment of the in vivo effect of (any) anticoagulant treatment could be assisted with the monitoring of fibrin-related markers (D-dimers; fibrin monomers)