Background There are two approaches to the treatment of atrialfibrillation: one is cardioversion and treatment with antiarrhythmicdrugs to maintain sinus rhythm, and the other is the use ofrate-controlling drugs, allowing atrial fibrillation to persist.In both approaches, the use of anticoagulant drugs is recommended.
Methods We conducted a randomized, multicenter comparison ofthese two treatment strategies in patients with atrial fibrillationand a high risk of stroke or death. The primary end point wasoverall mortality.
Results A total of 4060 patients (mean [±SD] age, 69.7±9.0years) were enrolled in the study; 70.8 percent had a historyof hypertension, and 38.2 percent had coronary artery disease.Of the 3311 patients with echocardiograms, the left atrium wasenlarged in 64.7 percent and left ventricular function was depressedin 26.0 percent. There were 356 deaths among the patients assignedto rhythm-control therapy and 310 deaths among those assignedto rate-control therapy (mortality at five years, 23.8 percentand 21.3 percent, respectively; hazard ratio, 1.15 [95 percentconfidence interval, 0.99 to 1.34]; P=0.08). More patients inthe rhythm-control group than in the rate-control group werehospitalized, and there were more adverse drug effects in therhythm-control group as well. In both groups, the majority ofstrokes occurred after warfarin had been stopped or when theinternational normalized ratio was subtherapeutic.
Conclusions Management of atrial fibrillation with the rhythm-controlstrategy offers no survival advantage over the rate-controlstrategy, and there are potential advantages, such as a lowerrisk of adverse drug effects, with the rate-control strategy.Anticoagulation should be continued in this group of high-riskpatients.
Source Information
The AFFIRM writing group (D.G. Wyse, A.L. Waldo, J.P. DiMarco, M.J. Domanski, Y. Rosenberg, E.B. Schron, J.C. Kellen, H.L. Greene, M.C. Mickel, J.E. Dalquist, and S.D. Corley) assumes overall responsibility for the content of the manuscript.
Address reprint requests to the AFFIRM Clinical Trial Center, Axio Research, 2601 4th Ave., Ste. 200, Seattle, WA 98121, or to leong{at}axioresearch.com.
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