Update on Anticoagulants Monitoring Practice
The direct oral anticoagulants (DOACs) currently include one direct thrombin inhibitor (dabigatran) and three direct factor Xa inhibitors (rivaroxaban, apixaban, edoxaban) which have various approvals for treatment and prevention of thromboembolic events, As opposed to more traditional anticoagulants, DOACs do not require routine laboratory monitoring due to predictable pharmacodynamics, pharmacokinetics, and wide therapeutic windows. DOACs have variable effects on routine coagulation tests, such as PT/INR and aPTT, depending on the specific drug, drug concentration in the specimen, patient and specific indication and dose, and assay, including the specific reagent used. Understanding DOAC effects on locally available routine coagulation tests may allow qualitative use of routine tests in emergent clinical situations but these tests do not reliably determine drug concentration. Although quantitative tests for the new drugs exist, they are not widely available, usually do not have turnaround times that would allow use in urgent clinical situations, and none are FDA approved. Aside from the issues with monitoring DOACs, it is also important for physicians and laboratory professionals to know that DOACs can interfere with specialized coagulation testing, such as thrombophilia testing, and that this testing should generally be avoided when DOACs are present.
