Mortality and morbidity reduction after frequent premature ventricular complexes ablation in patients with left ventricular systolic dysfunction.

Cardiac mortality Catheter ablation Left ventricular ejection fraction Premature ventricular complex burden Premature ventricular complexes Successful sustained ablation

Journal

Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology
ISSN: 1532-2092
Titre abrégé: Europace
Pays: England
ID NLM: 100883649

Informations de publication

Date de publication:
01 Jul 2019
Historique:
received: 11 10 2018
accepted: 07 03 2019
pubmed: 25 3 2019
medline: 3 11 2020
entrez: 25 3 2019
Statut: ppublish

Résumé

Ablation of frequent premature ventricular complexes (PVCs) improves left ventricular ejection fraction in patients with left ventricular (LV) systolic dysfunction. This study aims to evaluate the long-term hard outcomes and potential prognostic variables in this population. Prospective multicentre study including 101 consecutive patients [56 ± 12 years old, 62 (61%) men] with LV systolic dysfunction and frequent PVCs who underwent PVC ablation before November 2015. The last evaluation performed was considered the long-term follow-up (LTFUP) evaluation. Mean follow-up was 34 ± 16 months (range 24-84 months). Ablation was successful in 95 (94%) patients. There was a significant reduction in the PVC burden from 21 ± 12% at baseline to 3.8 ± 6% at LTFUP, P < 0.001. Left ventricular ejection fraction improved from 32 ± 8% at baseline to 39 ± 12% at LTFUP (P < 0.001) and New York Heart Association class from 2.2 ± 0.6% to 1.3 ± 0.6% (P < 0.001). Brain natriuretic peptide levels decreased from 136 (78-321) to 68 (32-144) pg/mL (P = 0.007). Most of this improvement occurs during the first 6 months after ablation. Persistent abolition of at least 18 points of the baseline PVC burden was independently and inversely associated with the composite endpoint of cardiac mortality, cardiac transplantation, or hospitalization for heart failure during follow-up [hazard ratio 0.18 (0.05-0.66), P = 0.01]. In patients with LV systolic dysfunction, ablation of frequent PVCs induces a significant improvement in functional, structural, and neurohormonal status, which persists at LTFUP. A sustained reduction in the baseline PVC burden is associated with a lower risk of cardiac mortality, cardiac transplantation, or hospitalization for heart failure during follow-up.

Identifiants

pubmed: 30904923
pii: 5419049
doi: 10.1093/europace/euz027
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1079-1087

Informations de copyright

Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2019. For permissions, please email: journals.permissions@oup.com.

Auteurs

Antonio Berruezo (A)

Heart Institute, Teknon Medical Center, C/Vilana, 12, Barcelona, Spain.

Diego Penela (D)

Ospedale Guglielmo da Saliceto, Piacenza, Italy.

Beatriz Jáuregui (B)

Heart Institute, Teknon Medical Center, C/Vilana, 12, Barcelona, Spain.

David Soto-Iglesias (D)

Heart Institute, Teknon Medical Center, C/Vilana, 12, Barcelona, Spain.

Luis Aguinaga (L)

Private Cardiology Center, Tucuman, Argentina.

Augusto Ordóñez (A)

Hospital Sant Pau i Santa Tecla, Tarragona, Spain.

Juan Fernández-Armenta (J)

Hospital Puerta del Mar, Cádiz, Spain.

Mikel Martínez (M)

Hospital Clínic and IDIBAPS, Barcelona, Spain.

Luis Tercedor (L)

Hospital Virgen de las Nieves, Granada, Spain.

Felipe Bisbal (F)

Heart Institute (iCor), Hospital Universitari Germans Trias i Pujol, Badalona, Spain.
CIBERCV, Instituto de Salud Carlos III, Madrid, Spain.

Juan Acosta (J)

Hospital Universitario Virgen del Rocío, Sevilla, Spain.

Julio Martí-Almor (J)

Hospital del Mar, Barcelona, Spain.

Marta Aceña (M)

Hospital de Bellvitge, Barcelona, Spain.

Ignasi Anguera (I)

Hospital de Bellvitge, Barcelona, Spain.

Luca Rossi (L)

Ospedale Guglielmo da Saliceto, Piacenza, Italy.

Markus Linhart (M)

Hospital Clínic and IDIBAPS, Barcelona, Spain.

Roger Borràs (R)

Hospital Clínic and IDIBAPS, Barcelona, Spain.

Adelina Doltra (A)

Hospital Clínic and IDIBAPS, Barcelona, Spain.

Paula Sánchez (P)

Hospital Clínic and IDIBAPS, Barcelona, Spain.

José T Ortiz-Pérez (JT)

Hospital Clínic and IDIBAPS, Barcelona, Spain.

Rosario J Perea (RJ)

Hospital Clínic and IDIBAPS, Barcelona, Spain.

Susana Prat-González (S)

Hospital Clínic and IDIBAPS, Barcelona, Spain.

Cheryl Teres (C)

Heart Institute, Teknon Medical Center, C/Vilana, 12, Barcelona, Spain.

Xavier Bosch (X)

Hospital Clínic and IDIBAPS, Barcelona, Spain.

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Classifications MeSH