Feasibility of leadless left ventricular septal pacing with the WiSE-CRT system to target the left bundle branch area: A porcine model and multicenter patient experience.

Cardiac resynchronization therapy Conduction system pacing Endocardial left ventricular pacing Heart failure Leadless pacing Left bundle branch area pacing

Journal

Heart rhythm
ISSN: 1556-3871
Titre abrégé: Heart Rhythm
Pays: United States
ID NLM: 101200317

Informations de publication

Date de publication:
12 2022
Historique:
received: 02 04 2022
revised: 01 07 2022
accepted: 16 07 2022
pubmed: 9 8 2022
medline: 6 12 2022
entrez: 8 8 2022
Statut: ppublish

Résumé

The WiSE-CRT system delivers leadless endocardial left ventricular (LV) pacing to achieve cardiac resynchronization therapy. The electrode is conventionally placed on the lateral wall, but implanting on the LV septum may have advantages, including capture of the left bundle branch, and improved battery longevity owing to reduced distance from the transmitter. The purpose of this study was to assess the feasibility of leadless LV septal pacing via the WiSE-CRT system. Two pigs underwent electrode implantation on the LV septum with subsequent anatomical and histological examination. Eight patients underwent implantation of the WiSE-CRT system with deployment of the electrode on the LV septum via an interatrial transseptal approach. Deployment of the electrode on the LV septum was successful in both animals. Histological examination demonstrated electrode tines in close proximity to Purkinje tissue. WiSE-CRT implantation with an LV septal electrode was successful in all patients. Biventricular capture was confirmed, with a significant reduction in QRS duration (187.1 ± 33.8 ms vs 149.5 ± 15.7 ms; P = .009). Temporary LV pacing achieved further QRS reduction (139.8 ± 12.4 ms), and in 4 patients the peak LV activation time in lead V Leadless LV septal pacing with the WiSE-CRT system to target the left bundle branch appears feasible. Further study is required to assess the efficacy and safety of this technique.

Sections du résumé

BACKGROUND
The WiSE-CRT system delivers leadless endocardial left ventricular (LV) pacing to achieve cardiac resynchronization therapy. The electrode is conventionally placed on the lateral wall, but implanting on the LV septum may have advantages, including capture of the left bundle branch, and improved battery longevity owing to reduced distance from the transmitter.
OBJECTIVE
The purpose of this study was to assess the feasibility of leadless LV septal pacing via the WiSE-CRT system.
METHODS
Two pigs underwent electrode implantation on the LV septum with subsequent anatomical and histological examination. Eight patients underwent implantation of the WiSE-CRT system with deployment of the electrode on the LV septum via an interatrial transseptal approach.
RESULTS
Deployment of the electrode on the LV septum was successful in both animals. Histological examination demonstrated electrode tines in close proximity to Purkinje tissue. WiSE-CRT implantation with an LV septal electrode was successful in all patients. Biventricular capture was confirmed, with a significant reduction in QRS duration (187.1 ± 33.8 ms vs 149.5 ± 15.7 ms; P = .009). Temporary LV pacing achieved further QRS reduction (139.8 ± 12.4 ms), and in 4 patients the peak LV activation time in lead V
CONCLUSION
Leadless LV septal pacing with the WiSE-CRT system to target the left bundle branch appears feasible. Further study is required to assess the efficacy and safety of this technique.

Identifiants

pubmed: 35940464
pii: S1547-5271(22)02188-9
doi: 10.1016/j.hrthm.2022.07.017
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1974-1983

Subventions

Organisme : Wellcome Trust
ID : WT203148/Z/16/Z
Pays : United Kingdom

Informations de copyright

Copyright © 2022 Heart Rhythm Society. Published by Elsevier Inc. All rights reserved.

Auteurs

Mark K Elliott (MK)

Department of Biomedical Engineering and Imaging Sciences, King's College London, London, United Kingdom; Department of Cardiology, Guy's and St Thomas' NHS Foundation Trust, London, United Kingdom. Electronic address: mark.elliott@kcl.ac.uk.

Pasquale Vergara (P)

Arrhythmia Unit and Electrophysiology Laboratories, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Nadeev Wijesuriya (N)

Department of Biomedical Engineering and Imaging Sciences, King's College London, London, United Kingdom; Department of Cardiology, Guy's and St Thomas' NHS Foundation Trust, London, United Kingdom.

Vishal S Mehta (VS)

Department of Biomedical Engineering and Imaging Sciences, King's College London, London, United Kingdom; Department of Cardiology, Guy's and St Thomas' NHS Foundation Trust, London, United Kingdom.

Paolo Bosco (P)

Department of Cardiology, Guy's and St Thomas' NHS Foundation Trust, London, United Kingdom.

Peggy Jacon (P)

Arrhythmias Unit, Grenoble Alpes University Hospital, Grenobles, France.

Michael Lee (M)

EBR Systems Inc, Sunnyvale, California.

Silvia Taloni (S)

EBR Systems Inc, Sunnyvale, California.

Steven Niederer (S)

Department of Biomedical Engineering and Imaging Sciences, King's College London, London, United Kingdom.

Jeffrey Alison (J)

MonashHeart, MonashHealth, Clayton, Victoria, Australia.

Olivier Piot (O)

Centre Cardiologique du Nord, Paris, France.

Paul R Roberts (PR)

Department of Cardiology, University Hospital Southampton NHS Foundation Trust, Southampton, United Kingdom.

John Paisey (J)

Department of Cardiology, University Hospital Southampton NHS Foundation Trust, Southampton, United Kingdom.

Pascal Defaye (P)

Arrhythmias Unit, Grenoble Alpes University Hospital, Grenobles, France.

Andrew Shute (A)

EBR Systems Inc, Sunnyvale, California.

Christopher A Rinaldi (CA)

Department of Biomedical Engineering and Imaging Sciences, King's College London, London, United Kingdom; Department of Cardiology, Guy's and St Thomas' NHS Foundation Trust, London, United Kingdom.

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