ECTOPIC trial: The efficacy of flEcainide Compared To metOprolol in reducing Premature ventrIcular contractions. A randomized open label cross-over study in pediatric patients.

Premature ventricular contractions anti-arrhythmic drugs children cross-over flecainide metoprolol randomized reduction

Journal

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

Informations de publication

Date de publication:
30 Jul 2024
Historique:
received: 07 06 2024
revised: 15 07 2024
accepted: 26 07 2024
medline: 2 8 2024
pubmed: 2 8 2024
entrez: 1 8 2024
Statut: aheadofprint

Résumé

Frequent premature ventricular contractions (PVCs) in children are usually considered benign. Symptoms and/or left ventricular dysfunction are indications for treatment with anti-arrhythmic drugs (AAD). To evaluate the efficacy of flecainide versus metoprolol in reducing PVCs in children. A randomized open label cross-over trial children with a PVC-burden of >15% on Holter; successively treated with metoprolol and flecainide or vice versa, with a drug free interval of at least two weeks. Holter measurements were repeated before and after the start of the AAD. Sixty patients were screened, 19 patients could be included. Median age was 13.9 years (IQR 5.5 years). Mean baseline PVC-burden was 21.7% (N=18, SD±14.0) before the start of flecainide and 21.2% (N=17, SD±11.5) before the start of metoprolol. In a mixed model analysis the estimated mean reduction in PVC-burden was 10.6 percentage-points (95%-CI 5.8-15.3) for flecainide and 2.4 percentage-points (95%-CI -2.7-7.5) for metoprolol, with a significant difference of 8.2 percentage-points (95%-CI of 0.86-15.46, P=0.031). Exploratory analysis revealed that 9/18 patients treated with flecainide and 1/17 patients treated with metoprolol, had a reduction to a PVC-burden below 5%. No discriminating factors between flecainide-responders and non-responders were found; the mean plasma level was not significantly different (0.34 mg/L versus 0.52 mg/L, P=0.277). In children with frequent PVCs flecainide led to a significant greater reduction of PVC-burden, compared to metoprolol. Flecainide was effective in only a subgroup of patients, which appears to be unrelated to the plasma level. (Dutch Trial Register number 26689).

Sections du résumé

BACKGROUND BACKGROUND
Frequent premature ventricular contractions (PVCs) in children are usually considered benign. Symptoms and/or left ventricular dysfunction are indications for treatment with anti-arrhythmic drugs (AAD).
OBJECTIVE OBJECTIVE
To evaluate the efficacy of flecainide versus metoprolol in reducing PVCs in children.
METHODS METHODS
A randomized open label cross-over trial children with a PVC-burden of >15% on Holter; successively treated with metoprolol and flecainide or vice versa, with a drug free interval of at least two weeks. Holter measurements were repeated before and after the start of the AAD.
RESULTS RESULTS
Sixty patients were screened, 19 patients could be included. Median age was 13.9 years (IQR 5.5 years). Mean baseline PVC-burden was 21.7% (N=18, SD±14.0) before the start of flecainide and 21.2% (N=17, SD±11.5) before the start of metoprolol. In a mixed model analysis the estimated mean reduction in PVC-burden was 10.6 percentage-points (95%-CI 5.8-15.3) for flecainide and 2.4 percentage-points (95%-CI -2.7-7.5) for metoprolol, with a significant difference of 8.2 percentage-points (95%-CI of 0.86-15.46, P=0.031). Exploratory analysis revealed that 9/18 patients treated with flecainide and 1/17 patients treated with metoprolol, had a reduction to a PVC-burden below 5%. No discriminating factors between flecainide-responders and non-responders were found; the mean plasma level was not significantly different (0.34 mg/L versus 0.52 mg/L, P=0.277).
CONCLUSIONS CONCLUSIONS
In children with frequent PVCs flecainide led to a significant greater reduction of PVC-burden, compared to metoprolol. Flecainide was effective in only a subgroup of patients, which appears to be unrelated to the plasma level. (Dutch Trial Register number 26689).

Identifiants

pubmed: 39089565
pii: S1547-5271(24)03090-X
doi: 10.1016/j.hrthm.2024.07.111
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Auteurs

Robin A Bertels (RA)

Willem-Alexander Children's Hospital - Leiden University Medical Center; Albinusdreef 2, Leiden, the Netherlands. Electronic address: r.a.bertels@lumc.nl.

Janneke A E Kammeraad (JAE)

Erasmus MC - Sophia Children's Hospital; Dr. Molewaterplein 40, Rotterdam, the Netherlands.

Nan van Geloven (N)

Department of Biomedical Data Sciences - Leiden University Medical Center, Albinusdreef 2, Leiden, the Netherlands.

Luc H Filippini (LH)

Juliana Children's Hospital - HAGA Hospital; Els Borst-Eilersplein 275, The Hague, the Netherlands.

Roel L F van der Palen (RLF)

Willem-Alexander Children's Hospital - Leiden University Medical Center; Albinusdreef 2, Leiden, the Netherlands.

Ramon O Tak (RO)

Department of pediatrics - St Antonius Hospital; Koekoekslaan 1, Nieuwegein, the Netherlands.

Stefan Frerich (S)

MosaKids Children's Hospital - Maastricht University Medical Center; P. Debyelaan 25, Maastricht, the Netherlands.

Ward Vanagt (W)

Beatrix Children's Hospital - University Medical Center Groningen; Hanzeplein 14, Groningen, the Netherlands.

Jan J B Rehbock (JJB)

Department of pediatrics - HAGA Hospital Zoetermeer; Toneellaan 1, Zoetermeer, the Netherlands.

Ingmar Knobbe (I)

Emma Children's Hospital - Amsterdam University Medical Centers; Meibergdreef 9, Amsterdam, the Netherlands.

Irene M Kuipers (IM)

Emma Children's Hospital - Amsterdam University Medical Centers; Meibergdreef 9, Amsterdam, the Netherlands.

Marta de Riva (M)

Department of Cardiology - Leiden University Medical Center, Albinusdreef 2, Leiden, the Netherlands.

Katja Zeppenfeld (K)

Department of Cardiology - Leiden University Medical Center, Albinusdreef 2, Leiden, the Netherlands.

Nico A Blom (NA)

Willem-Alexander Children's Hospital - Leiden University Medical Center; Albinusdreef 2, Leiden, the Netherlands; Emma Children's Hospital - Amsterdam University Medical Centers; Meibergdreef 9, Amsterdam, the Netherlands.

Classifications MeSH