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 | |||||||