Alcohol dose in septal ablation for hypertrophic obstructive cardiomyopathy.


Journal

International journal of cardiology
ISSN: 1874-1754
Titre abrégé: Int J Cardiol
Pays: Netherlands
ID NLM: 8200291

Informations de publication

Date de publication:
15 06 2021
Historique:
received: 23 12 2020
revised: 08 02 2021
accepted: 19 02 2021
pubmed: 2 3 2021
medline: 1 6 2021
entrez: 1 3 2021
Statut: ppublish

Résumé

The aim of this study was to evaluate short- and long-term outcomes related to dose of alcohol administered during alcohol septal ablation (ASA) in patients with hypertrophic obstructive cardiomyopathy (HOCM). Current guidelines recommend using 1-3 mL of alcohol administered in the target septal perforator artery, but this recommendation is based more on practical experience of interventionalists rather than on systematic evidence. We included 1448 patients and used propensity score to match patients who received a low-dose (1.0-1.9 mL) versus a high-dose (2.0-3.8 mL) of alcohol during ASA. The matched cohort analysis comprised 770 patients (n = 385 in both groups). There was a similar occurrence of 30-day post-procedural adverse events (13% vs. 12%; p = 0.59), and similar all-cause mortality rates (0.8% vs. 0.5%; p = 1) in the low-dose group and the high-dose group, respectively. In the long-term follow-up (5.4 ± 4.5 years), a total of 110 (14%) patients died representing 2.58 deaths and 2.64 deaths per 100 patient-years in the low dose and the high dose group (logrank, p = 0.92), respectively. There were no significant differences in the long-term dyspnea and left ventricular outflow gradient between the two groups. Patients treated with a low-dose of alcohol underwent more subsequent septal reduction procedures (logrank, p = 0.04). Matched HOCM patients undergoing ASA with a low-dose (1.0-1.9 mL) or a high-dose (2.0-3.8 mL) of alcohol had similar short- and long-term outcomes. A higher rate of repeated septal reduction procedures was observed in the group treated with a low-dose of alcohol.

Sections du résumé

BACKGROUND
The aim of this study was to evaluate short- and long-term outcomes related to dose of alcohol administered during alcohol septal ablation (ASA) in patients with hypertrophic obstructive cardiomyopathy (HOCM). Current guidelines recommend using 1-3 mL of alcohol administered in the target septal perforator artery, but this recommendation is based more on practical experience of interventionalists rather than on systematic evidence.
METHODS
We included 1448 patients and used propensity score to match patients who received a low-dose (1.0-1.9 mL) versus a high-dose (2.0-3.8 mL) of alcohol during ASA.
RESULTS
The matched cohort analysis comprised 770 patients (n = 385 in both groups). There was a similar occurrence of 30-day post-procedural adverse events (13% vs. 12%; p = 0.59), and similar all-cause mortality rates (0.8% vs. 0.5%; p = 1) in the low-dose group and the high-dose group, respectively. In the long-term follow-up (5.4 ± 4.5 years), a total of 110 (14%) patients died representing 2.58 deaths and 2.64 deaths per 100 patient-years in the low dose and the high dose group (logrank, p = 0.92), respectively. There were no significant differences in the long-term dyspnea and left ventricular outflow gradient between the two groups. Patients treated with a low-dose of alcohol underwent more subsequent septal reduction procedures (logrank, p = 0.04).
CONCLUSIONS
Matched HOCM patients undergoing ASA with a low-dose (1.0-1.9 mL) or a high-dose (2.0-3.8 mL) of alcohol had similar short- and long-term outcomes. A higher rate of repeated septal reduction procedures was observed in the group treated with a low-dose of alcohol.

Identifiants

pubmed: 33647367
pii: S0167-5273(21)00365-X
doi: 10.1016/j.ijcard.2021.02.056
pii:
doi:

Substances chimiques

Ethanol 3K9958V90M

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

127-132

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2021 The Authors. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors report no relationships that could be construed as a conflict of interest.

Auteurs

Josef Veselka (J)

Department of Cardiology, Second Medical School, Charles University, University Hospital Motol, Prague, Czech Republic. Electronic address: veselka.josef@seznam.cz.

Lothar Faber (L)

Ruhr-University Bochum, Germany.

Max Liebregts (M)

Department of Cardiology, St. Antonius Hospital Nieuwegein, Nieuwegein, the Netherlands.

Robert Cooper (R)

Institute of Cardiovascular Medicine and Science, Liverpool Heart and Chest Hospital, Liverpool, United Kingdom.

Jaroslav Januska (J)

Cardiocentre Podlesí, Třinec, Czech Republic.

Maksim Kashtanov (M)

Department of Endovascular Therapy, Sverdlovsk Regional Hospital N1 and Ural Federal University, Yekaterinburg, Russian Federation.

Maciej Dabrowski (M)

Department of Interventional Cardiology and Angiology, Institute of Cardiology, Warsaw, Poland.

Peter Riis Hansen (PR)

Department of Cardiology, Herlev and Gentofte Hospital, Hellerup, Denmark.

Hubert Seggewiss (H)

Deutsches Zentrum für Herzinsuffizienz, Universitätsklinikum Würzburg, Germany.

Jiri Bonaventura (J)

Department of Cardiology, Second Medical School, Charles University, University Hospital Motol, Prague, Czech Republic.

Eva Polakova (E)

Department of Cardiology, Second Medical School, Charles University, University Hospital Motol, Prague, Czech Republic.

Eva Hansvenclova (E)

Department of Cardiology, Second Medical School, Charles University, University Hospital Motol, Prague, Czech Republic.

Henning Bundgaard (H)

Unit for Inherited Cardiac Diseases, Department of Cardiology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.

Jurriën Ten Berg (J)

Department of Cardiology, St. Antonius Hospital Nieuwegein, Nieuwegein, the Netherlands.

Rodney Hilton Stables (RH)

Institute of Cardiovascular Medicine and Science, Liverpool Heart and Chest Hospital, Liverpool, United Kingdom.

Jiri Jarkovsky (J)

Institute of Biostatistics and Analyses, Faculty of Medicine and the Faculty of Science, Masaryk University, Brno, Czech Republic.

Morten Kvistholm Jensen (MK)

Unit for Inherited Cardiac Diseases, Department of Cardiology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.

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