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Sophia Antipolis, France – 29 Aug 2020: Patients with newly diagnosed atrial fibrillation benefit from early rhythm control therapy, according to results of the EAST-AFNET 4 trial presented in a Hot Line session today at ESC Congress 2020.1
Rhythm control therapy is typically delayed unless patients have persistent symptoms on otherwise effective rate control. The EAST-AFNET 4 trial investigated whether rhythm control therapy – with antiarrhythmic drugs or ablation – delivered soon after diagnosis improves outcomes.2,3
“The risk of severe cardiovascular complications and death in patients with atrial fibrillation is highest in the first year after diagnosis, suggesting that early therapy could be most beneficial,” said principal investigator Professor Paulus Kirchhof of the University Heart and Vascular Centre UKE Hamburg, Germany and University of Birmingham, UK. “Furthermore, atrial fibrillation causes atrial damage within a few weeks of disease onset. Early rhythm control therapy could reduce or prevent this damage, making it more effective.”
A total of 2,789 patients in the first year of atrial fibrillation diagnosis and with at least two cardiovascular conditions were enrolled from 135 sites in 11 countries during 2011 to 2016. Patients were randomised 1:1 to early rhythm control therapy or usual care, stratified by sites. Patients in both groups received treatment for cardiovascular conditions, anticoagulation, and rate control according to guidelines.
Patients in the early rhythm control group received antiarrhythmic drugs or catheter ablation (chosen by the local study teams). Rhythm control therapy was escalated when recurrent atrial fibrillation was documented clinically or by ECG, including monitoring with patient-operated ECG devices.
Patients in the usual care group were initially managed with rate control. Rhythm control therapy was only used to mitigate severe atrial fibrillation-related symptoms despite optimal rate control, following current guidelines.
The first primary outcome was a composite of cardiovascular death, stroke, worsening heart failure, and acute coronary syndrome. The second primary outcome was nights spent in hospital per year. The primary safety outcome was a composite of stroke, all-cause death, and serious adverse events caused by rhythm control therapy.
During a median follow-up of 5.1 years, the first primary outcome occurred in 249 patients on early therapy and in 316 patients receiving usual care. Adjusting for the group-sequential design of the trial, it occurred less often in patients on early rhythm control (hazard ratio [HR] 0.79; confidence interval [CI] 0.67–0.94; p=0.005). The absolute risk reduction with early rhythm control was 1.1% per year.
The clinical benefit of early rhythm control was consistent across subgroups, including asymptomatic patients and patients without heart failure. All components of the primary outcome occurred numerically less often in patients randomised to early therapy, and cardiovascular death and stroke were significantly reduced compared to usual care.
Regarding the second primary outcome, there was no difference in nights spent in hospital between groups (early therapy 5.8±21.9 days/year; usual care 5.1±15.5 days/year; p=0.226).
The primary safety outcome did not differ between groups (early therapy 231 events; usual care 223 events). Complications of rhythm control therapy were more common in patients on early therapy, but occurred infrequently, in line with other recent rhythm control trials.
Professor Kirchhof said: “Rhythm control therapy initiated soon after diagnosis of atrial fibrillation reduces cardiovascular complications without increasing time spent in hospital and without safety concerns. These results have the potential to completely change clinical practice towards rhythm control therapy early after the diagnosis of atrial fibrillation.”
Authors: ESC Press Office
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This press release accompanies both a presentation and an ESC press conference at ESC Congress 2020 – The Digital Experience. It does not necessarily reflect the opinion of the European Society of Cardiology.
Funding: AFNET, BMBF, DZHK, EHRA, Deutsche Herzstiftung, Abbott Laboratories, Sanofi.
Disclosures: Further support came from the European Union (grant agreement No 633196 [CATCH ME] to PK and AFNET. PK reports grants from DZHK / BMBF, Sanofi, Abbott, European Heart Rhythm Association / ESC, German Heart Foundation during the conduct of the study; PK has received research support from European Union (IMI 116074 [BigData@Heart]), British Heart Foundation (FS/13/43/30324; PG/17/30/32961; PG/20/22/35093; AA/18/2/34218), Leducq Foundation, Medical Research Council (UK), and German Centre for Heart Research, from several drug and device companies active in atrial fibrillation, and has received honoraria from several such companies, outside the submitted work. In addition, PK has a patent. PK is listed as inventor on two patents held by University of Birmingham (Atrial Fibrillation Therapy WO 2015140571, Markers for Atrial Fibrillation WO 2016012783) issued.
References and notes
1Abstract title: Early treatment of Atrial fibrillation for Stroke prevention Trial.
2The Early treatment of Atrial fibrillation for Stroke prevention Trial (EAST-AFNET 4). http://www.easttrial.org/
3Kirchhof P, Breithardt, Camm AJ, et al. Improving outcomes in patients with atrial fibrillation: rationale and design of the Early treatment of Atrial fibrillation for Stroke prevention Trial. Am Heart J. 2013;166:442–448.
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