Outcomes in anticoagulated patients with atrial fibrillation and with mitral or aortic valve disease
Language English Country England, Great Britain Media print-electronic
Document type Comparative Study, Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't
PubMed
29352007
DOI
10.1136/heartjnl-2017-312272
PII: heartjnl-2017-312272
Knihovny.cz E-resources
- Keywords
- aortic regurgitation, aortic stenosis, atrial fibrillation, mitral regurgitation, valvular heart disease,
- MeSH
- Anticoagulants therapeutic use MeSH
- Aortic Valve * MeSH
- Stroke epidemiology prevention & control MeSH
- Atrial Fibrillation complications MeSH
- Middle Aged MeSH
- Humans MeSH
- Mitral Valve * MeSH
- Heart Valve Diseases complications MeSH
- Pyrazoles therapeutic use MeSH
- Pyridones therapeutic use MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Treatment Outcome MeSH
- Warfarin therapeutic use MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Randomized Controlled Trial MeSH
- Comparative Study MeSH
- Names of Substances
- Anticoagulants MeSH
- apixaban MeSH Browser
- Pyrazoles MeSH
- Pyridones MeSH
- Warfarin MeSH
OBJECTIVE: To assess stroke/systemic embolism, major bleeding and other outcomes, and treatment effect of apixaban versus warfarin, in patients with atrial fibrillation (AF) and different types of valvular heart disease (VHD), using data from the Apixaban for Reduction in Stroke and Other Thromboembolic Events in Atrial Fibrillation trial. METHODS: There were 14 793 patients with known VHD status, categorised as having moderate or severe mitral regurgitation (MR) (n=3382), aortic regurgitation (AR) (n=842) or aortic stenosis (AS) (n=324); patients with moderate or severe mitral stenosis were excluded from the trial. Baseline characteristics, efficacy and safety outcomes were compared between each type and no significant VHD. Treatment effect was assessed using an adjusted model. RESULTS: Patients with MR or AR had similar rates of stroke/systemic embolism and bleeding compared with patients without MR or AR, respectively. Patients with AS had significantly higher event rates (presented as rate per 100 patient-years of follow-up) of stroke/systemic embolism (3.47 vs 1.36; adjusted HR (adjHR) 2.21, 95% CI 1.35 to 3.63), death (8.30 vs 3.53; adjHR 1.92, 95% CI 1.41 to 2.61), major bleeding (5.31 vs 2.53; adjHR 1.80, 95% CI 1.19 to 2.75) and intracranial bleeding (1.29 vs 0.51; adjHR 2.54, 95% CI 1.08 to 5.96) than patients without AS. The superiority of apixaban over warfarin on stroke/systemic embolism was similar in patients with versus without MR (HR 0.69, 95% CI 0.46 to 1.04 vs HR 0.79, 95% CI 0.63 to 1.00; interaction P value 0.52), with versus without AR (HR 0.57, 95% CI 0.27 to 1.20 vs HR 0.78, 95% CI 0.63 to 0.96; interaction P value 0.52), and with versus without AS (HR 0.44, 95% CI 0.17 to 1.13 vs HR 0.79, 95% CI 0.64 to 0.97; interaction P value 0.19). For each of the primary and secondary efficacy and safety outcomes, there was no evidence of a different effect of apixaban over warfarin in patients with any VHD subcategory. CONCLUSIONS: In anticoagulated patients with AF, AS is associated with a higher risk of stroke/systemic embolism, bleeding and death. The efficacy and safety benefits of apixaban compared with warfarin were consistent, regardless of presence of MR, AR or AS. CLINICAL TRIAL REGISTRATION: ARISTOTLE clinical trial number NCT00412984.
Bristol Myers Squibb Princeton New Jersey USA
Cardiology University and Emergency Hospital Bucharest Romania
Cardiology University of Medicine and Pharmacy Carol Davila Bucharest Romania
Dante Pazzanese Institute São Paulo University São Paulo Brazil
Duke Clinical Research Institute Duke University School of Medicine Durham North Carolina USA
Lady Davis Carmel Medical Center Haifa Israel
Mayo Clinic Rochester Minnesota USA
University Hospital Motol Prague Czech Republic
Uppsala Clinical Research Center Uppsala University Uppsala Sweden
References provided by Crossref.org
ClinicalTrials.gov
NCT00412984