Early Rhythm Control Therapy in Patients With Atrial Fibrillation and Heart Failure.


Journal

Circulation
ISSN: 1524-4539
Titre abrégé: Circulation
Pays: United States
ID NLM: 0147763

Informations de publication

Date de publication:
14 09 2021
Historique:
pubmed: 31 7 2021
medline: 30 12 2021
entrez: 30 7 2021
Statut: ppublish

Résumé

Even on optimal therapy, many patients with heart failure and atrial fibrillation experience cardiovascular complications. Additional treatments are needed to reduce these events, especially in patients with heart failure and preserved left ventricular ejection fraction. This prespecified subanalysis of the randomized EAST-AFNET4 trial (Early Treatment of Atrial Fibrillation for Stroke Prevention Trial) assessed the effect of systematic, early rhythm control therapy (ERC; using antiarrhythmic drugs or catheter ablation) compared with usual care (allowing rhythm control therapy to improve symptoms) on the 2 primary outcomes of the trial and on selected secondary outcomes in patients with heart failure, defined as heart failure symptoms New York Heart Association II to III or left ventricular ejection fraction [LVEF] <50%. This analysis included 798 patients (300 [37.6%] female, median age 71.0 [64.0, 76.0] years, 785 with known LVEF). The majority of patients (n=442) had heart failure and preserved LVEF (LVEF≥50%; mean LVEF 61±6.3%), the others had heart failure with midrange ejection fraction (n=211; LVEF 40%-49%; mean LVEF 44 ± 2.9%) or heart failure with reduced ejection fraction (n=132; LVEF<40%; mean LVEF 31±5.5%). Over the 5.1-year median follow-up, the composite primary outcome of cardiovascular death, stroke, or hospitalization for worsening of heart failure or for acute coronary syndrome occurred less often in patients randomly assigned to ERC (94/396; 5.7 per 100 patient-years) compared with patients randomly assigned to usual care (130/402; 7.9 per 100 patient-years; hazard ratio, 0.74 [0.56-0.97]; Rhythm control therapy conveys clinical benefit when initiated within 1 year of diagnosing atrial fibrillation in patients with signs or symptoms of heart failure. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT01288352. URL: http://www.controlled-trials.com; Unique identifier: ISRCTN04708680. URL: https://www.clinicaltrialsregister.eu; Unique identifier: 2010-021258-20.

Sections du résumé

BACKGROUND
Even on optimal therapy, many patients with heart failure and atrial fibrillation experience cardiovascular complications. Additional treatments are needed to reduce these events, especially in patients with heart failure and preserved left ventricular ejection fraction.
METHODS
This prespecified subanalysis of the randomized EAST-AFNET4 trial (Early Treatment of Atrial Fibrillation for Stroke Prevention Trial) assessed the effect of systematic, early rhythm control therapy (ERC; using antiarrhythmic drugs or catheter ablation) compared with usual care (allowing rhythm control therapy to improve symptoms) on the 2 primary outcomes of the trial and on selected secondary outcomes in patients with heart failure, defined as heart failure symptoms New York Heart Association II to III or left ventricular ejection fraction [LVEF] <50%.
RESULTS
This analysis included 798 patients (300 [37.6%] female, median age 71.0 [64.0, 76.0] years, 785 with known LVEF). The majority of patients (n=442) had heart failure and preserved LVEF (LVEF≥50%; mean LVEF 61±6.3%), the others had heart failure with midrange ejection fraction (n=211; LVEF 40%-49%; mean LVEF 44 ± 2.9%) or heart failure with reduced ejection fraction (n=132; LVEF<40%; mean LVEF 31±5.5%). Over the 5.1-year median follow-up, the composite primary outcome of cardiovascular death, stroke, or hospitalization for worsening of heart failure or for acute coronary syndrome occurred less often in patients randomly assigned to ERC (94/396; 5.7 per 100 patient-years) compared with patients randomly assigned to usual care (130/402; 7.9 per 100 patient-years; hazard ratio, 0.74 [0.56-0.97];
CONCLUSIONS
Rhythm control therapy conveys clinical benefit when initiated within 1 year of diagnosing atrial fibrillation in patients with signs or symptoms of heart failure. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT01288352. URL: http://www.controlled-trials.com; Unique identifier: ISRCTN04708680. URL: https://www.clinicaltrialsregister.eu; Unique identifier: 2010-021258-20.

Identifiants

pubmed: 34328366
doi: 10.1161/CIRCULATIONAHA.121.056323
pmc: PMC8456351
doi:

Substances chimiques

Anti-Arrhythmia Agents 0

Banques de données

ClinicalTrials.gov
['NCT01288352']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

845-858

Subventions

Organisme : British Heart Foundation
ID : FS/13/43/30324
Pays : United Kingdom
Organisme : British Heart Foundation
ID : AA/18/2/34218
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/18/33/33780
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/20/22/35093
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/17/30/32961
Pays : United Kingdom

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Auteurs

Andreas Rillig (A)

Department of Cardiology, University Heart and Vascular Center (A.R., C.M., P.K.), University Medical Center Hamburg-Eppendorf, Germany.
German Center for Cardiovascular Research, Partner Site Hamburg/Luebeck/Kiel (A.R., C.M., K.-H.K., K.W., P.K.).

Christina Magnussen (C)

Department of Cardiology, University Heart and Vascular Center (A.R., C.M., P.K.), University Medical Center Hamburg-Eppendorf, Germany.
German Center for Cardiovascular Research, Partner Site Hamburg/Luebeck/Kiel (A.R., C.M., K.-H.K., K.W., P.K.).

Ann-Kathrin Ozga (AK)

Institute of Medical Biometry and Epidemiology (A.-K.O., A.S., K.W.), University Medical Center Hamburg-Eppendorf, Germany.

Anna Suling (A)

Institute of Medical Biometry and Epidemiology (A.-K.O., A.S., K.W.), University Medical Center Hamburg-Eppendorf, Germany.

Axel Brandes (A)

Department of Cardiology, Odense University Hospital, Denmark (A.B.).
Department of Clinical Research, University of Southern Denmark, Odense (A.B.).

Günter Breithardt (G)

Atrial Fibrillation Network (AFNET), Münster, Germany (G.B., L.E., A.G., K.-H.K., K.W., P.K.).
Department of Cardiology II (Electrophysiology), University Hospital Münster, Germany (G.B., L.E.).

A John Camm (AJ)

Cardiology Clinical Academic Group, Molecular and Clinical Sciences Research Institute, St. George's University of London, United Kingdom (A.J.C.).

Harry J G M Crijns (HJGM)

Department of Cardiology, Maastricht University Medical Center and Cardiovascular Research Institute Maastricht, Netherlands (H.J.G.M.C.).

Lars Eckardt (L)

Atrial Fibrillation Network (AFNET), Münster, Germany (G.B., L.E., A.G., K.-H.K., K.W., P.K.).
Department of Cardiology II (Electrophysiology), University Hospital Münster, Germany (G.B., L.E.).

Arif Elvan (A)

Isala Hospital and Diagram Research, Zwolle, The Netherlands (A.E.).

Andreas Goette (A)

Atrial Fibrillation Network (AFNET), Münster, Germany (G.B., L.E., A.G., K.-H.K., K.W., P.K.).
St. Vincenz Hospital, Paderborn, Germany (A.G.).
Working Group of Molecular Electrophysiology, University Hospital Magdeburg, Germany (A.G.).

Michele Gulizia (M)

Garibaldi-Nesima-Hospital, Catania, Italy (M.G.).

Laurent Haegeli (L)

University Hospital Zurich, Zurich, Switzerland (L.H.).
Division of Cardiology, Medical University Department, Kantonsspital Aarau, Switzerland (L.H.).

Hein Heidbuchel (H)

University Hospital Antwerp and Antwerp University, Belgium (H.H.).

Karl-Heinz Kuck (KH)

German Center for Cardiovascular Research, Partner Site Hamburg/Luebeck/Kiel (A.R., C.M., K.-H.K., K.W., P.K.).
Atrial Fibrillation Network (AFNET), Münster, Germany (G.B., L.E., A.G., K.-H.K., K.W., P.K.).
LANS Cardio, Hamburg, Germany (K.-H.K.).

Andre Ng (A)

Department of Cardiovascular Sciences, University of Leicester, National Institute for Health Research Leicester Biomedical Research Centre, Glenfield Hospital, United Kingdom (A.N.).

Lukasz Szumowski (L)

Arrhythmia Center of the National Institute of Cardiology; Medical Division of Cardinal Stefan Wyszynski University in Warsaw, Poland (L.S.).

Isabelle van Gelder (I)

University of Groningen, University Medical Center Groningen, Netherlands (I.v.G.).

Karl Wegscheider (K)

Institute of Medical Biometry and Epidemiology (A.-K.O., A.S., K.W.), University Medical Center Hamburg-Eppendorf, Germany.
German Center for Cardiovascular Research, Partner Site Hamburg/Luebeck/Kiel (A.R., C.M., K.-H.K., K.W., P.K.).
Atrial Fibrillation Network (AFNET), Münster, Germany (G.B., L.E., A.G., K.-H.K., K.W., P.K.).

Paulus Kirchhof (P)

Department of Cardiology, University Heart and Vascular Center (A.R., C.M., P.K.), University Medical Center Hamburg-Eppendorf, Germany.
German Center for Cardiovascular Research, Partner Site Hamburg/Luebeck/Kiel (A.R., C.M., K.-H.K., K.W., P.K.).
Atrial Fibrillation Network (AFNET), Münster, Germany (G.B., L.E., A.G., K.-H.K., K.W., P.K.).
Institute of Cardiovascular Sciences, University of Birmingham, United Kingdom (P.K.).

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