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Interacting medication use and the treatment effects of apixaban versus warfarin : results from the ARISTOTLE Trial

Washam, Jeffrey B. (författare)
Duke Univ, Sch Med, Duke Clin Res Inst, Duke Heart Ctr, Box 3943 DUMC, Durham, NC 27710 USA
Hohnloser, Stefan H. (författare)
Goethe Univ Frankfurt, Frankfurt, Germany
Lopes, Renato D. (författare)
Duke Univ, Sch Med, Duke Clin Res Inst, Duke Heart Ctr, Box 3943 DUMC, Durham, NC 27710 USA
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Wojdyla, Daniel M. (författare)
Duke Univ, Sch Med, Duke Clin Res Inst, Duke Heart Ctr, Box 3943 DUMC, Durham, NC 27710 USA
Vinereanu, Dragos (författare)
Univ & Emergency Hosp Bucharest, Bucharest, Romania
Alexander, John H. (författare)
Duke Univ, Sch Med, Duke Clin Res Inst, Duke Heart Ctr, Box 3943 DUMC, Durham, NC 27710 USA
Gersh, Bernard J. (författare)
Mayo Clin, Coll Med, Rochester, MN USA
Hanna, Michael (författare)
Bristol Myers Squibb Co, Princeton, NJ USA
Horowitz, John (författare)
Univ Adelaide, Basil Hetzel Inst, Queen Elizabeth Hosp, Adelaide, SA, Australia
Hylek, Elaine M. (författare)
Boston Univ, Sch Med, Boston, MA 02118 USA
Xavier, Denis (författare)
St Johns Res Inst, Bengaluru, India
Verheugt, Freek W. A. (författare)
Univ Med Ctr Nijmegen, Nijmegen, Netherlands
Wallentin, Lars, 1943- (författare)
Uppsala universitet,Uppsala kliniska forskningscentrum (UCR)
Granger, Christopher B. (författare)
Duke Univ, Sch Med, Duke Clin Res Inst, Duke Heart Ctr, Box 3943 DUMC, Durham, NC 27710 USA
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 (creator_code:org_t)
2019-02-21
2019
Engelska.
Ingår i: Journal of Thrombosis and Thrombolysis. - : SPRINGER. - 0929-5305 .- 1573-742X. ; 47:3, s. 345-352
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Warfarin is dependent on multiple hepatic enzymes for metabolism while apixaban is a substrate for P-glycoprotein (P-gp) transport and hepatic CYP3A4 metabolism. The aim of this analysis was to assess the impact of interacting medication use on the treatment effects of apixaban versus warfarin. Outcomes were compared between apixaban and warfarin using Cox proportional hazards modeling according to the use of interacting medications at randomization in ARISTOTLE (n=18,201). Interacting medications for apixaban were identified as combined P-gp and 3A4 inhibitors or inducers while interacting medications for warfarin were defined as those highly probable for warfarin potentiation or inhibition. At randomization, 5547 (30.5%) patients were on an interacting medication, including 2722 on apixaban and 2825 on warfarin. Patients using an interacting medication were more likely to be female, taking aspirin, and have a history of prior bleeding and were less likely to have a prior stroke or transient ischemic attack. No significant differences were observed on the treatment effect of apixaban compared with warfarin in patients on and off interacting medications for outcomes including the primary efficacy outcome of stroke or systemic embolism (P for interaction=0.79) or the primary safety outcome of major bleeding (P for interaction=0.75). Use of interacting medications with anticoagulants occurs often in patients with atrial fibrillation. Despite the potential for altered exposure, interacting medication use was not associated with a significant change in the efficacy or safety of apixaban compared with warfarin in the ARISTOTLE trial.Trial registration ClinicalTrials.gov, NCT00412984

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kardiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)

Nyckelord

Atrial fibrillation
Interacting medications
Warfarin
Apixaban

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