Comparison of Left Bundle Branch Area Pacing and Biventricular Pacing in Candidates for Resynchronization Therapy.


Journal

Journal of the American College of Cardiology
ISSN: 1558-3597
Titre abrégé: J Am Coll Cardiol
Pays: United States
ID NLM: 8301365

Informations de publication

Date de publication:
18 07 2023
Historique:
received: 29 03 2023
revised: 05 05 2023
accepted: 08 05 2023
medline: 14 7 2023
pubmed: 24 5 2023
entrez: 23 5 2023
Statut: ppublish

Résumé

Cardiac resynchronization therapy (CRT) with biventricular pacing (BVP) is a well established therapy in patients with reduced left ventricular ejection fraction (LVEF), heart failure, and wide QRS or expected frequent ventricular pacing. Left bundle branch area pacing (LBBAP) has recently been shown to be a safe alternative to BVP. The aim of this study was to compare the clinical outcomes between BVP and LBBAP among patients undergoing CRT. This observational study included patients with LVEF ≤35% who underwent BVP or LBBAP for the first time for Class I or II indications for CRT from January 2018 to June 2022 at 15 international centers. The primary outcome was the composite endpoint of time to death or heart failure hospitalization (HFH). Secondary outcomes included endpoints of death, HFH, and echocardiographic changes. A total of 1,778 patients met inclusion criteria: 981 BVP, 797 LBBAP. The mean age was 69 ± 12 years, 32% were female, 48% had coronary artery disease, and mean LVEF was 27% ± 6%. Paced QRS duration in LBBAP was significantly narrower than baseline (128 ± 19 ms vs 161 ± 28 ms; P < 0.001) and significantly narrower compared to BVP (144 ± 23 ms; P < 0.001). Following CRT, LVEF improved from 27% ± 6% to 41% ± 13% (P < 0.001) with LBBAP compared with an increase from 27% ± 7% to 37% ± 12% (P < 0.001) with BVP, with significantly greater change from baseline with LBBAP (13% ± 12% vs 10% ± 12%; P < 0.001). On multivariable regression analysis, the primary outcome was significantly reduced with LBBAP compared with BVP (20.8% vs 28%; HR: 1.495; 95% CI: 1.213-1.842; P < 0.001). LBBAP improved clinical outcomes compared with BVP in patients with CRT indications and may be a reasonable alternative to BVP.

Sections du résumé

BACKGROUND
Cardiac resynchronization therapy (CRT) with biventricular pacing (BVP) is a well established therapy in patients with reduced left ventricular ejection fraction (LVEF), heart failure, and wide QRS or expected frequent ventricular pacing. Left bundle branch area pacing (LBBAP) has recently been shown to be a safe alternative to BVP.
OBJECTIVES
The aim of this study was to compare the clinical outcomes between BVP and LBBAP among patients undergoing CRT.
METHODS
This observational study included patients with LVEF ≤35% who underwent BVP or LBBAP for the first time for Class I or II indications for CRT from January 2018 to June 2022 at 15 international centers. The primary outcome was the composite endpoint of time to death or heart failure hospitalization (HFH). Secondary outcomes included endpoints of death, HFH, and echocardiographic changes.
RESULTS
A total of 1,778 patients met inclusion criteria: 981 BVP, 797 LBBAP. The mean age was 69 ± 12 years, 32% were female, 48% had coronary artery disease, and mean LVEF was 27% ± 6%. Paced QRS duration in LBBAP was significantly narrower than baseline (128 ± 19 ms vs 161 ± 28 ms; P < 0.001) and significantly narrower compared to BVP (144 ± 23 ms; P < 0.001). Following CRT, LVEF improved from 27% ± 6% to 41% ± 13% (P < 0.001) with LBBAP compared with an increase from 27% ± 7% to 37% ± 12% (P < 0.001) with BVP, with significantly greater change from baseline with LBBAP (13% ± 12% vs 10% ± 12%; P < 0.001). On multivariable regression analysis, the primary outcome was significantly reduced with LBBAP compared with BVP (20.8% vs 28%; HR: 1.495; 95% CI: 1.213-1.842; P < 0.001).
CONCLUSIONS
LBBAP improved clinical outcomes compared with BVP in patients with CRT indications and may be a reasonable alternative to BVP.

Identifiants

pubmed: 37220862
pii: S0735-1097(23)05546-8
doi: 10.1016/j.jacc.2023.05.006
pii:
doi:

Types de publication

Observational Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

228-241

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2023 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Funding Support and Author Disclosures Dr Vijayaraman has received honoraria and consultancy, research, and fellowship support from Medtronic; has served as a consultant for Abbott and Eaglepoint; has received honoraria from Boston Scientific and Biotronik; and has a patent for a His bundle pacing delivery tool. Dr Sharma has received honoraria from Medtronic; and has served as a consultant for Medtronic, Abbott, and Biotronik. Dr Cano has received honoraria from and served as a consultant for Medtronic, Biotronik, and Boston Scientific. Dr Ponnusamy has received honoraria from Medtronic. Dr Herweg has served as a speaker and consultant for Abbott; and has received speaking and fellowship support from Medtronic. Dr Jastrzebski has received honoraria from and served as a consultant for Medtronic and Abbott. Dr Zou has received honoraria from Abbott, Biotronik, Boston Scientific, Medtronic, and Microport. Dr Chelu has received research support from Patient-Centered Outcomes Research Institute, National Institutes of Health, Abbott, and Impulse Dynamics; and has received honorarium from Impulse Dynamics. Dr Vernooy has served as a consultant for Biosense Webster, Philips, Medtronic, Abbott, and Boston Scientific; and has received research and educational grants to his institution from Philips, Abbott, Medtronic, and Biosense Webster. Dr Whinnett has received honoraria from Medtronic and Boston Scientific; and has served as a consultant for Medtronic and Abbott. Dr Nair has received grants-in-aid from Biosense Webster, Medtronic, Canadian Institutes of Health Research, and Heart and Stroke Foundation of Canada; and has received honoraria and consulting fees from Medtronic, Biosense Webster, and Boston Scientific. Dr Curila has served as a consultant for and received honoraria from Medtronic, Biotronik, and Abbott. Dr Ellenbogen has served as a consultant for Medtronic, Boston Scientific, Abbott, and Biotronik; and has received honoraria from Medtronic, Boston Scientific, and Biotronik. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.

Auteurs

Pugazhendhi Vijayaraman (P)

Geisinger Heart Institute, Wilkes Barre, Pennsylvania, USA. Electronic address: pvijayaraman1@geisinger.edu.

Parikshit S Sharma (PS)

Rush University Medical Center, Chicago, Illinois, USA.

Óscar Cano (Ó)

Hospital Universitari i Politècnic La Fe and Centro de Investigaciones Biomédicas en RED en Enfermedades Cardiovasculares, Valencia, Spain.

Shunmuga Sundaram Ponnusamy (SS)

Velammal Medical College Hospital and Research Institute, Madurai, India.

Bengt Herweg (B)

University of South Florida Morsani College of Medicine, Tampa, Florida, USA.

Francesco Zanon (F)

Santa Maria Della Misericordia Hospital, Rovigo, Italy.

Marek Jastrzebski (M)

First Department of Cardiology, Interventional Electrocardiology and Hypertension, Jagiellonian University, Medical College, Krakow, Poland.

Jiangang Zou (J)

Cardiology, First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.

Mihail G Chelu (MG)

Baylor College of Medicine and Texas Heart Institute, Houston, Texas, USA.

Kevin Vernooy (K)

Department of Cardiology, Cardiovascular Research Institute Maastricht, Maastricht University Medical Center, Maastricht, the Netherlands.

Zachary I Whinnett (ZI)

National Heart and Lung Institute, Imperial College London, London, United Kingdom.

Girish M Nair (GM)

University of Ottawa Heart Institute, Ottawa, Ontario, Canada.

Manuel Molina-Lerma (M)

Hospital Universitario Virgen de las Nieves, Granada, Spain.

Karol Curila (K)

Cardiocenter, Third Faculty of Medicine, Charles University, Prague, Czech Republic.

Dipen Zalavadia (D)

Geisinger Heart Institute, Wilkes Barre, Pennsylvania, USA.

Abdul Haseeb (A)

Geisinger Heart Institute, Wilkes Barre, Pennsylvania, USA.

Cicely Dye (C)

Rush University Medical Center, Chicago, Illinois, USA.

Sharath C Vipparthy (SC)

Rush University Medical Center, Chicago, Illinois, USA.

Ryan Brunetti (R)

University of South Florida Morsani College of Medicine, Tampa, Florida, USA.

Pawel Moskal (P)

Electrophysiology Laboratory, University Hospital in Krakow, Krakow, Poland.

Alexandra Ross (A)

National Heart and Lung Institute, Imperial College London, London, United Kingdom.

Antonius van Stipdonk (A)

Department of Cardiology, Cardiovascular Research Institute Maastricht, Maastricht University Medical Center, Maastricht, the Netherlands.

Jerin George (J)

Baylor College of Medicine, Houston, Texas, USA.

Yusuf K Qadeer (YK)

Baylor College of Medicine, Houston, Texas, USA.

Mishal Mumtaz (M)

University of South Florida Morsani College of Medicine, Tampa, Florida, USA.

Jeffrey Kolominsky (J)

Virginia Commonwealth University Medical Center, Richmond, Virginia, USA.

Syeda A Zahra (SA)

National Heart and Lung Institute, Imperial College London, London, United Kingdom.

Mehrdad Golian (M)

University of Ottawa Heart Institute, Ottawa, Ontario, Canada.

Lina Marcantoni (L)

Santa Maria Della Misericordia Hospital, Rovigo, Italy.

Faiz A Subzposh (FA)

Geisinger Heart Institute, Wilkes Barre, Pennsylvania, USA.

Kenneth A Ellenbogen (KA)

Virginia Commonwealth University Medical Center, Richmond, Virginia, USA.

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