Cardiac resynchronization therapy in patients with a prior history of atrial fibrillation: Insights from four major clinical trials

Author:

Dalgaard Frederik123ORCID,Fudim Marat14,Al‐Khatib Sana M.145,Friedman Daniel J.14ORCID,Abraham William T.6,Cleland John G. F.7,Curtis Anne B.8ORCID,Gold Michael R.9ORCID,Kutyifa Valentina10ORCID,Linde Cecilia11,Young James12,Ali‐Ahmed Fatima1,Tang Anthony13,Olivas‐Martinez Antonio14,Inoue Lurdes Y. T.14,Sanders Gillian D.1451516

Affiliation:

1. Duke Clinical Research Institute Duke University School of Medicine Durham North Carolina USA

2. Department of Cardiology Herlev and Gentofte Hospital Copenhagen Denmark

3. Department of Medicine Nykøbing Falster Sygehus Nykøbing Denmark

4. Division of Cardiology Duke University School of Medicine Durham North Carolina USA

5. Department of Medicine Duke University School of Medicine Durham North Carolina USA

6. Division of Cardiovascular Medicine The Ohio State University Columbus Ohio USA

7. National Heart and Lung Institute, Royal Brompton & Harefield Hospitals Imperial College London UK

8. Department of Medicine University at Buffalo Buffalo New York USA

9. Medical University of South Carolina Charleston South Carolina USA

10. Division of Cardiology, Department of Medicine University of Rochester Medical Center Rochester Rochester New York USA

11. Department of Cardiology, Karolinska Institutet Karolinska University Hospital Stockholm Sweden

12. Cleveland Clinic, Lerner College of Medicine of Case Western Reserve University Cleveland Ohio USA

13. Department of Medicine Western University Ontario Canada

14. Department of Biostatistics University of Washington Seattle Washington USA

15. Duke‐Margolis Center for Health Policy Duke University Durham North Carolina USA

16. Evidence Synthesis Group, Duke Clinical Research Institute Duke University School of Medicine Durham North Carolina USA

Abstract

AbstractAimsTo investigate the association of cardiac resynchronization therapy (CRT) on outcomes among participants with and without a history of atrial fibrillation (AF).MethodsIndividual‐patient‐data from four randomized trials investigating CRT‐Defibrillators (COMPANION, MADIT‐CRT, REVERSE) or CRT‐Pacemakers (COMPANION, MIRACLE) were analyzed. Outcomes were time to a composite of heart failure hospitalization or all‐cause mortality or to all‐cause mortality alone. The association of CRT on outcomes for patients with and without a history of AF was assessed using a Bayesian‐Weibull survival regression model adjusting for baseline characteristics.ResultsOf 3964 patients included, 586 (14.8%) had a history of AF; 2245 (66%) were randomized to CRT. Overall, CRT reduced the risk of the primary composite endpoint (hazard ratio [HR]: 0.69, 95% credible interval [CI]: 0.56–0.81). The effect was similar (posterior probability of no interaction = 0.26) in patients with (HR: 0.78, 95% CI: 0.55–1.10) and without a history of AF (HR: 0.67, 95% CI: 0.55–0.80). In these four trials, CRT did not reduce mortality overall (HR: 0.82, 95% CI: 0.66–1.01) without evidence of interaction (posterior probability of no interaction = 0.14) for patients with (HR: 1.09, 95% CI: 0.70–1.74) or without a history of AF (HR: 0.70, 95% CI: 0.60–0.97).ConclusionThe association of CRT on the composite endpoint or mortality was not statistically different for patients with or without a history of AF, but this could reflect inadequate power. Our results call for trials to confirm the benefit of CRT recipients with a history of AF.

Publisher

Wiley

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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