CRT-D replacement strategy: results of the BioCONTINUE study.


Journal

Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing
ISSN: 1572-8595
Titre abrégé: J Interv Card Electrophysiol
Pays: Netherlands
ID NLM: 9708966

Informations de publication

Date de publication:
Aug 2023
Historique:
received: 01 09 2022
accepted: 25 11 2022
medline: 12 7 2023
pubmed: 3 12 2022
entrez: 2 12 2022
Statut: ppublish

Résumé

In patients with cardiac resynchronization therapy defibrillators (CRT-Ds), the need for implantable cardioverter-defibrillator (ICD) back-up may be questionable at time of CRT-D replacement (REP) if ICD implant criteria are no longer met due to an improved left ventricular ejection fraction (LVEF) and if no major ventricular arrhythmic event (VAE) occurred during the CRT-D lifetime. The aim of our study was to assess the relevance of ICD back-up and predictors of VAE after REP in primary prevention CRT-D patients. The prospective, observational, international BioCONTINUE study investigated the rate of patients with at least 1 sustained VAE (sVAE) post-REP and searched for predictive factors of sVAE. Two hundred seventy-six patients (70 ± 10 years, 77% men, mean LVEF 40.6 ± 12.6%) were followed for 28.4 ± 10.2 months. The rate of patients with sVAE was 8.3%, 10.3%, and 21.2% at 1, 2, and 4 years post-REP. Patients without persistent ICD indication at REP still had a sVAE rate of 5.7% (95% CI 2.3-11.5%) at 2 years. In multivariate analysis, predictive factors of subsequent sVAE were (i) persistent ICD indication (hazard ratio (HR) 3.6; 95% CI 1.6-8.3; p = 0.003); (ii) 64-72 years of age as compared to ≥ 79 years (HR 3.7; 95% CI 1.4-9.7; p = 0.008); and (iii) ischemic heart disease (HR 4.4; 95% CI 2.1-9.3; p < 0.0001). The risk of sVAE (21.2% at 4 years post-REP) depends on age, ischemic heart disease, and ICD indication at the time of REP. A non-trivial risk of sVAE remains in patients without persistent ICD indication. NCT02323503.

Sections du résumé

BACKGROUND BACKGROUND
In patients with cardiac resynchronization therapy defibrillators (CRT-Ds), the need for implantable cardioverter-defibrillator (ICD) back-up may be questionable at time of CRT-D replacement (REP) if ICD implant criteria are no longer met due to an improved left ventricular ejection fraction (LVEF) and if no major ventricular arrhythmic event (VAE) occurred during the CRT-D lifetime. The aim of our study was to assess the relevance of ICD back-up and predictors of VAE after REP in primary prevention CRT-D patients.
METHODS METHODS
The prospective, observational, international BioCONTINUE study investigated the rate of patients with at least 1 sustained VAE (sVAE) post-REP and searched for predictive factors of sVAE.
RESULTS RESULTS
Two hundred seventy-six patients (70 ± 10 years, 77% men, mean LVEF 40.6 ± 12.6%) were followed for 28.4 ± 10.2 months. The rate of patients with sVAE was 8.3%, 10.3%, and 21.2% at 1, 2, and 4 years post-REP. Patients without persistent ICD indication at REP still had a sVAE rate of 5.7% (95% CI 2.3-11.5%) at 2 years. In multivariate analysis, predictive factors of subsequent sVAE were (i) persistent ICD indication (hazard ratio (HR) 3.6; 95% CI 1.6-8.3; p = 0.003); (ii) 64-72 years of age as compared to ≥ 79 years (HR 3.7; 95% CI 1.4-9.7; p = 0.008); and (iii) ischemic heart disease (HR 4.4; 95% CI 2.1-9.3; p < 0.0001).
CONCLUSIONS CONCLUSIONS
The risk of sVAE (21.2% at 4 years post-REP) depends on age, ischemic heart disease, and ICD indication at the time of REP. A non-trivial risk of sVAE remains in patients without persistent ICD indication.
CLINICAL TRIAL REGISTRATION BACKGROUND
NCT02323503.

Identifiants

pubmed: 36459310
doi: 10.1007/s10840-022-01440-5
pii: 10.1007/s10840-022-01440-5
doi:

Banques de données

ClinicalTrials.gov
['NCT02323503']

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1201-1209

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

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Auteurs

Daniel Gras (D)

Hôpital Privé du Confluent, 2-4 Rue Eric Tabarly, 44200, Nantes, France. dangras@aol.com.

Nicolas Clémenty (N)

Centre Hospitalier Universitaire Tours, Tours, France.

Sylvain Ploux (S)

IHU Liryc, Electrophysiology and Heart Modeling Institute, Fondation Bordeaux Université, Bordeaux University Hospital (CHU), Cardio-Thoracic Unit, 33600, Pessac, France.

Yves Guyomar (Y)

Centre Hospitalier Saint Philibert, Lomme, France.

Damien Legallois (D)

Centre Hospitalier Universitaire Caen, Caen, France.

Luca Segreti (L)

Hospital Santa Chiara, Cisanello, Italy.

Hugues Blangy (H)

Hôpital Brabois, Nancy, France.

Gabriel Laurent (G)

Centre Hospitalier Universitaire du Bocage, Dijon, France.

Olivier Bizeau (O)

Centre Hospitalier Régional Orléans La Source, Orléans, France.

Sophie Fauquembergue (S)

BIOTRONIK France SAS, Rungis, France.

Arnaud Lazarus (A)

Clinique Ambroise Paré, Neuilly Sur Seine, France.

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