| Literature DB >> 32267996 |
Robyn Konicki1, Daniel Weiner1, J Herbert Patterson1, Daniel Gonzalez1, Angela Kashuba1, Yanguang Carter Cao1, Anil K Gehi2, Paul Watkins1, J Robert Powell1.
Abstract
Rivaroxaban is a direct-acting oral anticoagulant (DOAC) approved to prevent strokes in patients with atrial fibrillation (AF). Dosage recommendations are approved for all adult patients to receive either 15 mg or 20 mg once daily depending upon renal function. There are a number of reasons to believe rivaroxaban dosing could be more effective and/or safer for more patients if increased dosing precision is available. Since real world patients are more diverse than those studied in Phase III clinical trials, we evaluated the extremes of creatinine clearance (CrCl) on rivaroxaban clearance using a published population pharmacokinetic model and applying exposure variation limits (± 20%) based on published literature. The proposed dosing recommendations are 10 mg once daily (QD) (CrCl 15-29 mL/min), 15 mg QD (30-69 mL/min), 10 mg twice daily (BID) (70-159 mL/min) and 15 mg BID (160-250 mL/min). These new dosing recommendations should be prospectively tested for predictive accuracy and to assess the impact on AF patient efficacy and safety. This article is protected by copyright. All rights reserved.Entities:
Keywords: direct oral anticoagulants; population pharmacokinetics; precision dosing; precision medicine; rivaroxaban
Year: 2020 PMID: 32267996 DOI: 10.1111/cts.12766
Source DB: PubMed Journal: Clin Transl Sci ISSN: 1752-8054 Impact factor: 4.689