Leadless left ventricular endocardial pacing in nonresponders to conventional cardiac resynchronization therapy.


Journal

Pacing and clinical electrophysiology : PACE
ISSN: 1540-8159
Titre abrégé: Pacing Clin Electrophysiol
Pays: United States
ID NLM: 7803944

Informations de publication

Date de publication:
09 2020
Historique:
received: 13 02 2020
revised: 23 03 2020
accepted: 19 04 2020
pubmed: 25 4 2020
medline: 13 10 2021
entrez: 25 4 2020
Statut: ppublish

Résumé

Endocardial pacing may be beneficial in patients who fail to improve following conventional epicardial cardiac resynchronization therapy (CRT). The potential to pace anywhere inside the left ventricle thus avoiding myocardial scar and targeting the latest activating segments may be particularly important. The WiSE-CRT system (EBR systems, Sunnyvale, CA) reliably produces wireless, endocardial left ventricular (LV) pacing. The purpose of this analysis was to determine whether this system improved symptoms or led to LV remodeling in patients who were nonresponders to conventional CRT. An international, multicenter registry of patients who were nonresponders to conventional CRT and underwent implantation with the WiSE-CRT system was collected. Twenty-two patients were included; 20 patients underwent successful implantation with confirmation of endocardial biventricular pacing and in 2 patients, there was a failure of electrode capture. Eighteen patients proceeded to 6-month follow-up; endocardial pacing resulted in a significant reduction in QRS duration compared with intrinsic QRS duration (26.6 ± 24.4 ms; P = .002) and improvement in left ventricular ejection fraction (LVEF) (4.7 ± 7.9%; P = .021). The mean reduction in left ventricular end-diastolic volume was 8.3 ± 42.3 cm Nonresponders to conventional CRT have few remaining treatment options. We have shown in this high-risk patient group that the WiSE-CRT system results in improvement in their clinical composite scores and leads to LV remodeling.

Sections du résumé

BACKGROUND
Endocardial pacing may be beneficial in patients who fail to improve following conventional epicardial cardiac resynchronization therapy (CRT). The potential to pace anywhere inside the left ventricle thus avoiding myocardial scar and targeting the latest activating segments may be particularly important. The WiSE-CRT system (EBR systems, Sunnyvale, CA) reliably produces wireless, endocardial left ventricular (LV) pacing. The purpose of this analysis was to determine whether this system improved symptoms or led to LV remodeling in patients who were nonresponders to conventional CRT.
METHOD
An international, multicenter registry of patients who were nonresponders to conventional CRT and underwent implantation with the WiSE-CRT system was collected.
RESULTS
Twenty-two patients were included; 20 patients underwent successful implantation with confirmation of endocardial biventricular pacing and in 2 patients, there was a failure of electrode capture. Eighteen patients proceeded to 6-month follow-up; endocardial pacing resulted in a significant reduction in QRS duration compared with intrinsic QRS duration (26.6 ± 24.4 ms; P = .002) and improvement in left ventricular ejection fraction (LVEF) (4.7 ± 7.9%; P = .021). The mean reduction in left ventricular end-diastolic volume was 8.3 ± 42.3 cm
CONCLUSION
Nonresponders to conventional CRT have few remaining treatment options. We have shown in this high-risk patient group that the WiSE-CRT system results in improvement in their clinical composite scores and leads to LV remodeling.

Identifiants

pubmed: 32330307
doi: 10.1111/pace.13926
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

966-973

Informations de copyright

© 2020 The Authors. Pacing and Clinical Electrophysiology published by Wiley Periodicals LLC.

Références

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Auteurs

Baldeep S Sidhu (BS)

School of Biomedical Engineering and Imaging Sciences, King's College London, London, UK.
Guy's and St Thomas' Hospital, London, UK.

Bradley Porter (B)

School of Biomedical Engineering and Imaging Sciences, King's College London, London, UK.
Guy's and St Thomas' Hospital, London, UK.

Justin Gould (J)

School of Biomedical Engineering and Imaging Sciences, King's College London, London, UK.
Guy's and St Thomas' Hospital, London, UK.

Benjamin Sieniewicz (B)

School of Biomedical Engineering and Imaging Sciences, King's College London, London, UK.
Guy's and St Thomas' Hospital, London, UK.

Mark Elliott (M)

School of Biomedical Engineering and Imaging Sciences, King's College London, London, UK.
Guy's and St Thomas' Hospital, London, UK.

Vishal Mehta (V)

School of Biomedical Engineering and Imaging Sciences, King's College London, London, UK.
Guy's and St Thomas' Hospital, London, UK.

Peter P H M Delnoy (PPHM)

Isala Heart Center, Zwolle, the Netherlands.

Jean-Claude Deharo (JC)

Hopital La Timone, Marseille, France.

Christian Butter (C)

Immanuel Klinikum Bernau Herzzentrum Brandenburg, Bernau, Germany.

Martin Seifert (M)

Immanuel Klinikum Bernau Herzzentrum Brandenburg, Bernau, Germany.

Lucas V A Boersma (LVA)

St Antonius Ziekenhuis, Nieuwegein, Utrecht, the Netherlands.
Academic Medical Centre, University of Amsterdam, Amsterdam, the Netherlands.

Sam Riahi (S)

Aalborg University Hospital, Aalborg, Denmark.

Simon James (S)

The James Cook University Hospital, South Tees Hospitals NHS Foundation Trust, Middlesbrough, UK.

Andrew J Turley (AJ)

The James Cook University Hospital, South Tees Hospitals NHS Foundation Trust, Middlesbrough, UK.

Angelo Auricchio (A)

Fondazione Cardiocentro Ticino, Lugano, Switzerland.

Timothy R Betts (TR)

Oxford University Hospitals NHS Foundation Trust, Oxford, UK.

Steven Niederer (S)

School of Biomedical Engineering and Imaging Sciences, King's College London, London, UK.

Prashanthan Sanders (P)

Centre for Heart Rhythm Disorders, University of Adelaide and Royal Adelaide Hospital, Adelaide, South Australia, Australia.

Christopher A Rinaldi (CA)

School of Biomedical Engineering and Imaging Sciences, King's College London, London, UK.
Guy's and St Thomas' Hospital, London, UK.

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