Table 3.
Criteria for DOAC use | Comment(s) |
---|---|
Patient preference for and willingness to take DOAC | Patients should be presented will all therapeutic options and their respective perceived advantages and disadvantages (See Table 2) |
No contraindication to DOAC therapy | E.g. pregnancy, breastfeeding, mechanical heart valve |
Adequate organ function | Clinicians should regularly monitor renal function, particularly for DOACs with greater reliance on renal elimination (see Tables 5, 6 and 12) and, if there are other factors that may increase DOAC exposure (e.g. age, unavoidable use of concomitant p-gp/CYP3A4 inhibitors). Avoid in moderate or severe hepatic dysfunction |
No significant drug–drug interactions | See Tables 13 and 14 for detailed guidance Patients taking any anticoagulant with antiplatelet agents or NSAIDs have a significantly higher risk of bleeding. To minimize bleeding, avoid these drug combinations when possible |
No significant disease state interactions | VTE patients with a history of GI bleeding or at risk for GI bleeding may be better candidates for warfarin, apixaban, or edoxaban, as there may be a higher risk of bleeding or GI adverse effects with dabigatran and rivaroxaban |
Highly likely to be adherent with DOAC therapy and follow-up plan | See Table 4 for further details |
Confirmed ability to obtain DOAC on a longitudinal basis from a financial, insurance coverage and retail availability standpoint | The drug costs of DOACs may be prohibitive for some patients, as compared with generic warfarin plus laboratory monitoring There are patient assistance programs available via the pharmaceutical companies, and this should be arranged prior to prescribing |