Challenge and Impact of Quinidine Access in Sudden Death Syndromes: A National Experience.


Journal

JACC. Clinical electrophysiology
ISSN: 2405-5018
Titre abrégé: JACC Clin Electrophysiol
Pays: United States
ID NLM: 101656995

Informations de publication

Date de publication:
03 2019
Historique:
received: 15 06 2018
revised: 11 10 2018
accepted: 15 10 2018
entrez: 23 3 2019
pubmed: 23 3 2019
medline: 3 4 2020
Statut: ppublish

Résumé

This study sought to determine the nature of quinidine use and accessibility in a national network of inherited arrhythmia clinics. Quinidine is an antiarrhythmic medication that has been shown to be beneficial in select patients with Brugada syndrome, early repolarization syndrome, and idiopathic ventricular fibrillation. Because of the low prevalence of these conditions and restricted access to quinidine through a single regulatory process, quinidine use is rare in Canada. Subjects prescribed quinidine were identified through the Hearts in Rhythm Organization that connects the network of inherited arrhythmia clinics across Canada. Cases were retrospectively reviewed for patient characteristics, indications for quinidine use, rate of recurrent ventricular arrhythmia, and issues with quinidine accessibility. In a population of 36 million, 46 patients are currently prescribed quinidine (0.0000013%, age 48.1 ± 16.1 years, 25 are male). Brugada syndrome, early repolarization syndrome, and idiopathic ventricular fibrillation constituted a diagnosis in 13 subjects (28%), 6 (13%), and 21 (46%), respectively. Overall, 37 subjects (81%) had cardiac arrest as an index event. After initial presentation, subjects experienced 7.47 ± 12.3 implantable cardioverter-defibrillator shocks prior to quinidine use over 34.3 ± 45.9 months, versus 0.86 ± 1.69 implantable cardioverter-defibrillator shocks in 43.8 ± 41.8 months while on quinidine (risk ratio: 8.7, p < 0.001). Twenty-two patients access quinidine through routes external to Health Canada's Special Access Program. Quinidine use is rare in Canada, but it is associated with a reduction in recurrent ventricular arrhythmias in patients with Brugada syndrome, early repolarization syndrome, and idiopathic ventricular fibrillation, with minimal toxicity necessitating discontinuation. Drug interruption is associated with frequent breakthrough events. Access to quinidine is important to deliver this potentially lifesaving therapy.

Sections du résumé

OBJECTIVES
This study sought to determine the nature of quinidine use and accessibility in a national network of inherited arrhythmia clinics.
BACKGROUND
Quinidine is an antiarrhythmic medication that has been shown to be beneficial in select patients with Brugada syndrome, early repolarization syndrome, and idiopathic ventricular fibrillation. Because of the low prevalence of these conditions and restricted access to quinidine through a single regulatory process, quinidine use is rare in Canada.
METHODS
Subjects prescribed quinidine were identified through the Hearts in Rhythm Organization that connects the network of inherited arrhythmia clinics across Canada. Cases were retrospectively reviewed for patient characteristics, indications for quinidine use, rate of recurrent ventricular arrhythmia, and issues with quinidine accessibility.
RESULTS
In a population of 36 million, 46 patients are currently prescribed quinidine (0.0000013%, age 48.1 ± 16.1 years, 25 are male). Brugada syndrome, early repolarization syndrome, and idiopathic ventricular fibrillation constituted a diagnosis in 13 subjects (28%), 6 (13%), and 21 (46%), respectively. Overall, 37 subjects (81%) had cardiac arrest as an index event. After initial presentation, subjects experienced 7.47 ± 12.3 implantable cardioverter-defibrillator shocks prior to quinidine use over 34.3 ± 45.9 months, versus 0.86 ± 1.69 implantable cardioverter-defibrillator shocks in 43.8 ± 41.8 months while on quinidine (risk ratio: 8.7, p < 0.001). Twenty-two patients access quinidine through routes external to Health Canada's Special Access Program.
CONCLUSIONS
Quinidine use is rare in Canada, but it is associated with a reduction in recurrent ventricular arrhythmias in patients with Brugada syndrome, early repolarization syndrome, and idiopathic ventricular fibrillation, with minimal toxicity necessitating discontinuation. Drug interruption is associated with frequent breakthrough events. Access to quinidine is important to deliver this potentially lifesaving therapy.

Identifiants

pubmed: 30898241
pii: S2405-500X(18)30827-2
doi: 10.1016/j.jacep.2018.10.007
pii:
doi:

Substances chimiques

Anti-Arrhythmia Agents 0
Quinidine ITX08688JL

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

376-382

Subventions

Organisme : CIHR
ID : MOP-142218
Pays : Canada
Organisme : CIHR
ID : SRG-15-P09-001
Pays : Canada

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2019 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Auteurs

Navraj Malhi (N)

University of British Columbia, Vancouver, British Columbia, Canada.

Christopher C Cheung (CC)

University of British Columbia, Vancouver, British Columbia, Canada.

Bishoy Deif (B)

Western University, London, Ontario, Canada.

Jason D Roberts (JD)

Western University, London, Ontario, Canada.

Lorne J Gula (LJ)

Western University, London, Ontario, Canada.

Martin S Green (MS)

University of Ottawa Heart Institute, Ottawa, Ontario, Canada.

Benjamin Pang (B)

University of Ottawa Heart Institute, Ottawa, Ontario, Canada.

Omar Sultan (O)

University of Saskatchewan, Regina Qu'Appelle Health Region, Regina, Saskatchewan, Canada.

Kaja M Konieczny (KM)

St. Michael's Hospital, Toronto, Ontario, Canada.

Paul Angaran (P)

St. Michael's Hospital, Toronto, Ontario, Canada.

Paul Dorian (P)

St. Michael's Hospital, Toronto, Ontario, Canada.

Ilan Lashevsky (I)

Schulich Heart Centre, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Ontario, Canada.

Jeff S Healey (JS)

Population Health Research Institute, McMaster University, Hamilton, Ontario, Canada.

Aiman Alak (A)

Population Health Research Institute, McMaster University, Hamilton, Ontario, Canada.

Rafik Tadros (R)

Department of Medicine, University of Montreal, Research Center, Montreal Heart Institute, Montreal, Quebec, Canada.

Antoine Andorin (A)

Department of Medicine, University of Montreal, Research Center, Montreal Heart Institute, Montreal, Quebec, Canada.

Christian Steinberg (C)

Laval University, Quebec Heart and Lung Institute, Inherited Arrhythmia Clinic, Quebec City, Quebec, Canada.

Felix Ayala-Paredes (F)

Université de Sherbrooke, Faculté de Médecine et des Sciences de la Santé, Montreal, Quebec, Canada.

Christopher S Simpson (CS)

Queen's University, Kingston, Ontario, Canada.

Joseph Atallah (J)

University of Alberta School of Public Health, Faculty of Medicine and Dentistry, Edmonton, Alberta, Canada.

Andrew D Krahn (AD)

University of British Columbia, Vancouver, British Columbia, Canada. Electronic address: akrahn@mail.ubc.ca.

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Classifications MeSH