Table 3.
Patient Group | Suitability for Novel OAC | Comments |
---|---|---|
Eligible for oral anticoagulation, unwilling or unable to take a VKA | Novel OAC should be considered. | May include patients with allergy or increased sensitivity to VKAs, or those not receiving VKA because of fear of bleeding (particularly ICH). |
Eligible for oral anticoagulation, naïve to VKA (newly diagnosed) | All available options, including VKAs and novel OACs, should be considered. | Factors influencing therapeutic choice should include contraindications for novel OACs (eg, creatinine clearance <15 mL/min; see Table 4) and costs (direct and indirect). |
Receiving VKA with unstable INR | Novel OAC should be considered depending on reason for INR instability. | If INR is unstable because of nonadherence, novel OAC therapy may not be an improvement over VKA therapy. If INR is unstable because of drug or food/alcohol interactions, novel OAC therapy may be beneficial. If INR is frequently higher than the therapeutic range, novel OAC therapy may be beneficial to reduce the risk of ICH. |
Receiving VKA with stable INR | Limited justification for novel OAC (in the absence of other factors). |
Benefits of VKAs are greater in patients with good INR control. Transition between anticoagulants requires careful management. Dabigatran is associated with gastrointestinal tolerability issues. |
Abbreviations: ICH, intracranial hemorrhage; INR, international normalized ratio; OAC, oral anticoagulant; VKA, vitamin K antagonist.