New-onset versus prior history of atrial fibrillation: Outcomes from the AFFIRM trial.
Autor: | Damluji AA; Cardiovascular Division, University of Miami Miller School of Medicine, Miami, FL., Al-Damluji MS; Department of Internal Medicine, Yale University School of Medicine, New Haven, CT., Marzouka GR; Cardiovascular Division, University of Miami Miller School of Medicine, Miami, FL., Coffey JO; Cardiovascular Division, University of Miami Miller School of Medicine, Miami, FL., Viles-Gonzalez JF; Cardiovascular Division, University of Miami Miller School of Medicine, Miami, FL., Cohen MG; Cardiovascular Division, University of Miami Miller School of Medicine, Miami, FL., Moscucci M; Cardiovascular Division, University of Miami Miller School of Medicine, Miami, FL., Myerburg RJ; Cardiovascular Division, University of Miami Miller School of Medicine, Miami, FL., Mitrani RD; Cardiovascular Division, University of Miami Miller School of Medicine, Miami, FL. Electronic address: RMitrani@med.miami.edu. |
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Jazyk: | angličtina |
Zdroj: | American heart journal [Am Heart J] 2015 Jul; Vol. 170 (1), pp. 156-63, 163.e1. Date of Electronic Publication: 2015 Apr 24. |
DOI: | 10.1016/j.ahj.2015.04.020 |
Abstrakt: | Background: There are limited data on prognosis and outcomes of patients with new-onset atrial fibrillation (AF) compared with those with a prior history of AF. Methods and Results: We conducted a comparison of these 2 groups in the AFFIRM trial. New-onset AF was the qualifying arrhythmia in 1,391 patients (34%). Compared with patients with prior history of AF, patients with new-onset AF were more likely to have a history of heart failure. There was no mortality difference between rate control (RaC) and rhythm control (RhC) among patients with new-onset AF (17% vs 20%, P = .152). In the univariate model, new-onset AF was associated with increased risk of mortality compared with history of prior AF (RaC unadjusted hazard ratio [HR] 1.36 [P = .010], RhC unadjusted HR 1.39 [P = .003]). However, after multivariate adjustments, new-onset AF did not carry an increased risk of mortality (RaC adjusted HR 1.14 [P = .370], RhC adjusted HR 1.16 [P = .248]). Subjects with new-onset AF randomized to the RhC arm were more likely to remain in normal sinus rhythm at follow-up (adjusted HR 0.79, P = .012) compared with patients with prior history of AF. Conclusions: In a multivariable analysis adjusting for confounders, new-onset AF was not associated with increased mortality compared with prior history of AF regardless of the treatment strategy. Patients with new-onset AF treated with the rhythm control strategy were more likely to remain in normal sinus rhythm on follow-up. (Copyright © 2015 Elsevier Inc. All rights reserved.) |
Databáze: | MEDLINE |
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