Safety and Effectiveness of Pulsed Field Ablation for Atrial Fibrillation in Patients With Heart Failure.

HFpEF HFrEF atrial fibrillation heart failure pulsed field ablation

Journal

JACC. Clinical electrophysiology
ISSN: 2405-5018
Titre abrégé: JACC Clin Electrophysiol
Pays: United States
ID NLM: 101656995

Informations de publication

Date de publication:
18 May 2024
Historique:
received: 19 04 2024
revised: 01 05 2024
accepted: 01 05 2024
medline: 12 6 2024
pubmed: 12 6 2024
entrez: 12 6 2024
Statut: aheadofprint

Résumé

Atrial fibrillation (AF) and heart failure (HF) coexist, increasing morbidity and mortality. Studies have demonstrated improved outcomes following AF ablation in HF patients with reduced ejection fraction (EF). This study sought to assess the outcomes of pulsed field ablation (PFA) in HF. MANIFEST-PF (Multi-National Survey on the Methods, Efficacy, and Safety on the Post-Approval Clinical Use of Pulsed Field Ablation) is a multicenter, patient-level registry of consecutive patients undergoing PFA for paroxysmal AF or persistent AF (PerAF). In this substudy, patients were stratified as no history of HF (no-HF), HF with preserved EF (HFpEF) (left ventricular EF of ≥50%) or HF with reduced/mildly reduced EF (HFmr/rEF) (left ventricular EF of <50%). The primary effectiveness and safety endpoints were freedom from documented atrial arrhythmias lasting ≥30 seconds and major adverse events, respectively. Of the 1,381 patients, 85% (n = 1,174) were no-HF, 6.2% (n = 87) were HFpEF, and 8.6% (n = 120) were HFmr/rEF. No-HF patients had less PerAF than patients with HF (P < 0.001), with no difference between HF subtypes (P = >0.99). The 1-year freedom from atrial arrhythmia was significantly higher in no-HF patients than in those with HFpEF or HFmr/rEF (79.9%, 71.3%, and 67.5%, respectively; P < 0.001) but similar between patients with HFmr/rEF and HFpEF (P = 0.26). However, there was no significant difference in freedom from atrial arrhythmia among patients with no-HF vs HFpEF vs HFmr/rEF for those with paroxysmal AF (82.8%, 82.4%, and 71.7%, respectively; P = 0.09) and PerAF (73.3%, 64.2%, and 64.9%, respectively; P = 0.14). Major adverse event rates were similar between the no-HF, HFpEF, and HFmr/rEF groups (1.9%, 0%, and 2.5%, respectively). PFA appears to be potentially safe and effective in AF patients with HF. Freedom from atrial arrhythmia post-PFA was higher in patients without a history of HF, with no significant difference between HF subtypes.

Sections du résumé

BACKGROUND BACKGROUND
Atrial fibrillation (AF) and heart failure (HF) coexist, increasing morbidity and mortality. Studies have demonstrated improved outcomes following AF ablation in HF patients with reduced ejection fraction (EF).
OBJECTIVE OBJECTIVE
This study sought to assess the outcomes of pulsed field ablation (PFA) in HF.
METHODS METHODS
MANIFEST-PF (Multi-National Survey on the Methods, Efficacy, and Safety on the Post-Approval Clinical Use of Pulsed Field Ablation) is a multicenter, patient-level registry of consecutive patients undergoing PFA for paroxysmal AF or persistent AF (PerAF). In this substudy, patients were stratified as no history of HF (no-HF), HF with preserved EF (HFpEF) (left ventricular EF of ≥50%) or HF with reduced/mildly reduced EF (HFmr/rEF) (left ventricular EF of <50%). The primary effectiveness and safety endpoints were freedom from documented atrial arrhythmias lasting ≥30 seconds and major adverse events, respectively.
RESULTS RESULTS
Of the 1,381 patients, 85% (n = 1,174) were no-HF, 6.2% (n = 87) were HFpEF, and 8.6% (n = 120) were HFmr/rEF. No-HF patients had less PerAF than patients with HF (P < 0.001), with no difference between HF subtypes (P = >0.99). The 1-year freedom from atrial arrhythmia was significantly higher in no-HF patients than in those with HFpEF or HFmr/rEF (79.9%, 71.3%, and 67.5%, respectively; P < 0.001) but similar between patients with HFmr/rEF and HFpEF (P = 0.26). However, there was no significant difference in freedom from atrial arrhythmia among patients with no-HF vs HFpEF vs HFmr/rEF for those with paroxysmal AF (82.8%, 82.4%, and 71.7%, respectively; P = 0.09) and PerAF (73.3%, 64.2%, and 64.9%, respectively; P = 0.14). Major adverse event rates were similar between the no-HF, HFpEF, and HFmr/rEF groups (1.9%, 0%, and 2.5%, respectively).
CONCLUSIONS CONCLUSIONS
PFA appears to be potentially safe and effective in AF patients with HF. Freedom from atrial arrhythmia post-PFA was higher in patients without a history of HF, with no significant difference between HF subtypes.

Identifiants

pubmed: 38864809
pii: S2405-500X(24)00351-7
doi: 10.1016/j.jacep.2024.05.002
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Funding Support and Author Disclosures Boston Scientific provided a grant to help fund data collection but was not otherwise involved with study design or analysis and did not have access to this manuscript before submission. Dr Turagam has received consulting fees from Biosense Webster, Boston Scientific Inc, and AltaThera and speaker honoraria from Sanofi and Medtronic. Dr Neuzil has received a grant from the Ministry of Health, Czech Republic, Development of Research Organizations (DRO), Na Homolka Hospital (NHH) (0023884). Dr Schmidt has received speaker fees and research grants from Boston Scientific/Farapulse, Medtronic, Biosense Webster, and Abbott. Dr Reichlin has received research grants from the Swiss National Science Foundation, the Swiss Heart Foundation, and the sitem insel support fund; speaker/consulting honoraria or travel support from Abbott/SJM, Bayer, Biosense Webster, Biotronik, Boston Scientific, Daiichi Sankyo, Medtronic, and Pfizer-BMS; and support for his institution’s fellowship program from Abbott/SJM, Biosense Webster, Biotronik, Boston Journal Pre-proof 21 Scientific, and Medtronic. Dr Neven has received speaker fees from Farapulse, Inc. Dr Metzner has received a research grant and fees from Farapulse. Dr Hansen has received speaker fees and grant support from Biosense Webster and Medtronic. Dr Blaauw has received research grants from Medtronic and Atricure and consulting fees from Abbott, Biosense Webster, Boston Scientific. Dr Sommer has served as a member of the Advisory Board for Abbott, Biosense Webster, Boston Scientific, and Medtronic. He has received modest honoraria from Medtronic. Dr Anic has received consultant fees from Farapulse Inc, Boston Scientific Inc, Galaxy Medical Inc, and Biosense Webster and has performed contracted research for Farapulse Inc, Boston Scientific Inc, Galaxy Medical Inc, and Biosense Webster. Dr Anselme has received consulting fees from Boston Scientific, Medtronic, and Microport CRM. Dr Boveda has received consulting fees from Medtronic, Boston Scientific, Microport, Zoll, and BMS. Dr Deneke has received speaker honoraria from Galaxy Medical, Abbott, and Biotronik, has been a consultant to Farapulse, and has served on a Clinical Events Committee for Boston Scientific. Dr Willems has received grants and personal fees from Abbott, Boston Scientific, and Medtronic and personal fees from Boehringer Ingelheim, Brystol Myers Squibb, Bayer Vital, Accutus, Daiichi, and Farapulse Inc. Dr Tilz has received consulting fees from Boston Scientific, Abbott Medical, Biotronik, and Biosense Webster and speaker honoraria from Boston Scientific, Abbott Medical, Biotronik, and Biosense Webster. Dr Scherr has received an educational grant from Farapulse Inc and is a consultant for Boston Scientific Inc. Dr Wakili has received investigator-initiated funding for research projects (initiated by him) from Bristol Myers Squibb, Pfizer, and Boston Scientific and speaking honoraria from Boston Scientific, Biotronik, and Medtronic. Dr Steven has received speaker fees from Pfizer, Bayer, Abbott, Johnson & Johnson, and Medtronic; grants from Abbott, Johnson & Johnson, and Boston Scientific; and consulting fees from Boston Scientific and Johnson & Johnson. Dr Kautzner has received personal fees from Bayer, Biosense Webster, Boehringer Ingelheim, Medtronic, and Abbott for participation in Scientific Advisory Boards and speaker honoraria from Bayer, Biosense Webster, Biotronik, Boehringer Ingelheim, CathVision, Medtronic, Mylan, Pfizer, ProMed, and Abbott. Dr Jais has received partial funding from L'institut Des Maladies Du Rythme Cardiaque, LIRYC ANR-10-IAHU-04, equity from Farapulse, and consulting fees and a grant from Boston Scientific. Dr Chun has received speaker fees and research grants from Boston Scientific/Farapulse, Medtronic, Biosense Webster, and Abbott. Dr Roten has received research grants from Medtronic, the Swiss National Foundation, the Swiss Heart Foundation, the Immanuel and Ilse Straub Foundation, and the Sitem Insel Support Fund and speaker fees/honoraria from Biosense Webster, Boston Scientific, Abbott, and Medtronic. Dr Lemoine has received a research grant from Farapulse. Dr Rollin has received a research grant from Farapulse. Dr Gunawardene has received grants from Farapulse Inc and Abbott. Dr Heeger has received travel grants and research grants from Boston Scientific, Lifetech, Biosense Webster, and Cardiofocus and speaker honoraria from Boston Scientific, Lifetech. Biosense Webster, Bayer, and Cardiofocus and he has served as a consultant for Medtronic, Journal Pre-proof 22 Lifetech, Boston Scientific, Biosense Webster, and Cardiofocus. Dr Manninger has received speaker fees from Bayer, Biosense Webster, Biotronik, Amomed, AOP Orphan, Boston Scientific, Daiichi Sankyo, and BMS/Pfizer and research grants from Biosense Webster and Abbott. Dr Sultan has received lecture and consulting honoraria from Medtronic, Abbott, and Bayer. Dr Derval has received receiving consulting fees from Boston Scientific. Dr Reddy has received consulting fees (and equity—now divested) from Farapulse Inc; has served as a consultant for Boston Scientific Inc; unrelated to this manuscript, has also served as a consultant for and has equity in Ablacon, Acutus Medical, Affera-Medtronic, Anumana, Apama Medical–Boston Scientific, APN Health, Aquaheart, Atacor, Autonomix, Axon Therapies, Backbeat, BioSig, CardiaCare, Cardiofocus, CardioNXT/AFTx, Circa Scientific, CoRISMA, Corvia Medical, Dinova-Hangzhou DiNovA EP Technology, East End Medical, EPD-Philips, EP Frontiers, Epix Therapeutics–Medtronic, EpiEP, Eximo, Field Medical, Focused Therapeutics, HRT, Intershunt, Javelin, Kardium, Keystone Heart, Laminar Medical, LuxMed, Medlumics, Middlepeak, Neutrace, Nuvera–Biosense Webster, Oracle Health, Restore Medical, Sirona Medical, SoundCath, and Valcare; unrelated to this work, has served as a consultant for Abbott, Adagio Medical, Append Medical, AtriAN, Biosense Webster, BioTel Heart, Biotronik, Cairdac, Cardionomic, CoreMap, Fire1, Gore & Associates, Impulse Dynamics, Medtronic, Novartis, Novo Nordisk, Philips, Pulse Biosciences; and unrelated to this work, has equity in Atraverse, DRS Vascular, Manual Surgical Sciences, Newpace, Nyra Medical, Soundcath, Surecor, and Vizaramed. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.

Auteurs

Mohit K Turagam (MK)

Icahn School of Medicine at Mount Sinai, New York, New York, USA.

Petr Neuzil (P)

Cardiology Department, Na Homolce Hospital, Homolka Hospital, Prague, Czech Republic.

Boris Schmidt (B)

Medizinisches Versorgungszentrum CCB Frankfurt und Main-Taunus GbR, Frankfurt, Germany.

Tobias Reichlin (T)

Inselspital-Bern University Hospital, University of Bern, Bern, Switzerland.

Kars Neven (K)

Department of Medicine, Witten/Herdecke University, Witten, Germany; Department of Electrophysiology, Alfried Krupp Hospital, Essen, Germany.

Andreas Metzner (A)

University Heart and Vascular Center, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Jim Hansen (J)

Department of Cardiology, Herlev-Gentofte University Hospital, Hellerup, Denmark.

Yuri Blaauw (Y)

Department of Cardiology, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.

Philippe Maury (P)

Department of Cardiology, University Hospital Rangueil, Toulouse, France; Institute of Metabolic and Cardiovascular Diseases, INSERM UMR 1297, Toulouse, France.

Thomas Arentz (T)

Department of Cardiology and Angiology, Medical Center and Faculty of Medicine, University of Freiburg, Germany.

Philipp Sommer (P)

Clinic for Electrophysiology, Herz- und Diabeteszentrum Nordrhein-Westfalen, Ruhr-University Bochum, Bad Oeynhausen, Germany.

Ante Anic (A)

Department for Cardiovascular Diseases, University Hospital Center Split, Split, Croatia.

Frederic Anselme (F)

Department of Cardiology, Rouen Hospital, Rouen, France.

Serge Boveda (S)

Heart Rhythm Department, Clinique Pasteur, Toulouse, France; Universitair Ziekenhuis, Brussels, Belgium.

Tom Deneke (T)

Heart Center Bad Neustadt, Rhoen-Clinic Campus Bad Neustadt, Bad Neustadt an der Saale, Germany.

Stephan Willems (S)

Asklepios Hospital St Georg, Hamburg, Germany.

Pepijn van der Voort (P)

Catharina Ziekenhuis, Eindhoven, the Netherlands.

Roland Tilz (R)

University Heart Center Lübeck, Department of Rhythmology, University Hospital Schleswig-Holstein, Germany; German Center for Cardiovascular Research, Partner Site Hamburg/Kiel/Lübeck, Lübeck, Germany.

Moritoshi Funasako (M)

Cardiology Department, Na Homolce Hospital, Homolka Hospital, Prague, Czech Republic; Neuron Medical, Brno, Czech Republic.

Daniel Scherr (D)

Division of Cardiology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.

Reza Wakili (R)

Department of Cardiology and Vascular Medicine, West German Heart and Vascular Center Essen, University Duisburg-Essen, Duisburg, Germany.

Daniel Steven (D)

Department for Electrophysiology, Heart Center University Hospital of Cologne, Cologne, Germany.

Josef Kautzner (J)

IKEM-Institute for Clinical and Experimental Medicine, Prague, Czech Republic.

Johan Vijgen (J)

Department of Cardiology, Jessa Hospitals, Hasselt, Belgium.

Pierre Jais (P)

L'institut Des Maladies Du Rythme Cardiaque, LIRYC, CHU Bordeaux, University of Bordeaux, Bordeaux, France.

Jan Petru (J)

Cardiology Department, Na Homolce Hospital, Homolka Hospital, Prague, Czech Republic.

Julian Chun (J)

Medizinisches Versorgungszentrum CCB Frankfurt und Main-Taunus GbR, Frankfurt, Germany.

Laurent Roten (L)

Inselspital-Bern University Hospital, University of Bern, Bern, Switzerland.

Anna Füting (A)

Department of Medicine, Witten/Herdecke University, Witten, Germany; Department of Electrophysiology, Alfried Krupp Hospital, Essen, Germany.

Marc D Lemoine (MD)

University Heart and Vascular Center, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Martin Ruwald (M)

Department of Cardiology, Herlev-Gentofte University Hospital, Hellerup, Denmark.

Bart A Mulder (BA)

Department of Cardiology, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.

Anne Rollin (A)

Department of Cardiology, University Hospital Rangueil, Toulouse, France.

Heiko Lehrmann (H)

Department of Cardiology and Angiology, Medical Center and Faculty of Medicine, University of Freiburg, Germany.

Thomas Fink (T)

Clinic for Electrophysiology, Herz- und Diabeteszentrum Nordrhein-Westfalen, Ruhr-University Bochum, Bad Oeynhausen, Germany.

Zrinka Jurisic (Z)

Department for Cardiovascular Diseases, University Hospital Center Split, Split, Croatia.

Corentin Chaumont (C)

Department of Cardiology, Rouen Hospital, Rouen, France.

Raquel Adelino (R)

Heart Rhythm Department, Clinique Pasteur, Toulouse, France; Universitair Ziekenhuis, Brussels, Belgium.

Karin Nentwich (K)

Heart Center Bad Neustadt, Rhoen-Clinic Campus Bad Neustadt, Bad Neustadt an der Saale, Germany.

Melanie Gunawardene (M)

Asklepios Hospital St Georg, Hamburg, Germany.

Alexandre Ouss (A)

Catharina Ziekenhuis, Eindhoven, the Netherlands.

Christian-Hendrik Heeger (CH)

University Heart Center Lübeck, Department of Rhythmology, University Hospital Schleswig-Holstein, Germany; German Center for Cardiovascular Research, Partner Site Hamburg/Kiel/Lübeck, Lübeck, Germany.

Martin Manninger (M)

Division of Cardiology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.

Jan-Eric Bohnen (JE)

Department of Cardiology and Vascular Medicine, West German Heart and Vascular Center Essen, University Duisburg-Essen, Duisburg, Germany.

Arian Sultan (A)

Department for Electrophysiology, Heart Center University Hospital of Cologne, Cologne, Germany.

Petr Peichl (P)

IKEM-Institute for Clinical and Experimental Medicine, Prague, Czech Republic.

Pieter Koopman (P)

Department of Cardiology, Jessa Hospitals, Hasselt, Belgium.

Nicolas Derval (N)

L'institut Des Maladies Du Rythme Cardiaque, LIRYC, CHU Bordeaux, University of Bordeaux, Bordeaux, France.

Thomas Kueffer (T)

Inselspital-Bern University Hospital, University of Bern, Bern, Switzerland.

Nico Reinsch (N)

Department of Medicine, Witten/Herdecke University, Witten, Germany; Department of Electrophysiology, Alfried Krupp Hospital, Essen, Germany.

Vivek Y Reddy (VY)

Icahn School of Medicine at Mount Sinai, New York, New York, USA; Cardiology Department, Na Homolce Hospital, Homolka Hospital, Prague, Czech Republic. Electronic address: vivek.reddy@mountsinai.org.

Classifications MeSH