Table 2. Indications for laboratory measurement of direct-acting oral anticoagulants (DOACs)2,33,34,36-38.
| Clinical indication | Examples of clinical scenarios | Comment about DOAC measurement |
|---|---|---|
| Emergency scenarios requiring normal haemostasis | • To assess the utility of an anticoagulant antidote during an acute life-threatening bleeding event • To assess the safety of proceeding with an urgent surgical procedure with high bleeding risk • Pre-thrombolytic therapy assessment for acute stroke |
Drug concentration assays: For all DOACs, drug concentration assays provide a precise gauge. A concentration below 30 micrograms/L may be used for proceeding with invasive procedures. Coagulation function assays: For apixaban and rivaroxaban, coagulation function assays are not recommended because of insufficient sensitivity to anticoagulant effect. For dabigatran, the coagulation function assay TCT has excellent sensitivity, and a result within normal reference range is consistent with absence of clinically significant dabigatran concentrations. APTT and PT are not useful. |
| Scenarios suggestive of excessive DOAC exposure | • Haemorrhagic event • Suspected overdose • Severe acute kidney injury • Concomitant medicines that inhibit CYP3A enzyme or P-glycoprotein transporter |
Drug concentration assays: Measure drug concentration and consult local laboratory or an anticoagulation expert for interpretation of results. Coagulation function assays: Coagulation function assays are difficult to interpret to provide a gauge of DOAC exposure. |
| Scenarios suggestive of inadequate DOAC exposure | • Thrombotic event • Malabsorptive gastrointestinal conditions • Concomitant medicines that induce CYP3A enzyme or P-glycoprotein transporter |
As per Scenarios suggestive of excessive DOAC exposure |
APTT = activated partial thromboplastin time; CYP = cytochrome P450; PT = prothrombin time; TCT = thrombin clotting time