The Prevalence and Characteristics of Arrhythmic Mitral Valve Prolapse in Patients With Unexplained Cardiac Arrest.

arrhythmic mitral valve prolapse idiopathic ventricular fibrillation mitral valve prolapse strength of diagnosis unexplained cardiac arrest

Journal

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

Informations de publication

Date de publication:
06 Sep 2023
Historique:
received: 10 04 2023
revised: 25 07 2023
accepted: 02 08 2023
medline: 7 10 2023
pubmed: 7 10 2023
entrez: 7 10 2023
Statut: aheadofprint

Résumé

There is growing evidence that mitral valve prolapse (MVP) is associated with otherwise unexplained cardiac arrest (UCA). However, reports are hindered by the absence of a systematic ascertainment of alternative diagnoses. This study reports the prevalence and characteristics of MVP in a large cohort of patients with UCA. Patients were enrolled following an UCA, defined as cardiac arrest with no coronary artery disease, preserved left ventricular ejection fraction, and no apparent explanation on electrocardiogram. A comprehensive evaluation was performed, and patients were diagnosed with idiopathic ventricular fibrillation (IVF) if no cause was found. Echocardiography reports were reviewed for MVP. Patients with MVP were divided into 2 groups: those with IVF (AMVP) and those with an alternative diagnosis (nonarrhythmic MVP). Patient characteristics were then compared. The long-term outcomes of AMVP were reported. Among 571 with an initially UCA, 34 patients had MVP (6%). The prevalence of definite MVP was significantly higher in patients with IVF than those with an alternative diagnosis (24 of 366 [6.6%] vs 5 of 205 [2.4%]; P = 0.03). Bileaflet prolapse was significantly associated with AMVP (18 of 23 [78%] vs 1 of /8 [12.5%]; P = 0.001; OR: 25.2). The proportion of patients with AMVP who received appropriate implantable cardioverter-defibrillator therapies over a median follow-up of 42 months was 21.1% (4 of 19). MVP is associated with otherwise UCA (IVF), with a prevalence of 6.6%. Bileaflet prolapse appears to be a feature of AMVP, although future studies need to ascertain its independent association. A significant proportion of patients with AMVP received appropriate implantable cardioverter-defibrillator therapies during follow-up.

Sections du résumé

BACKGROUND BACKGROUND
There is growing evidence that mitral valve prolapse (MVP) is associated with otherwise unexplained cardiac arrest (UCA). However, reports are hindered by the absence of a systematic ascertainment of alternative diagnoses.
OBJECTIVES OBJECTIVE
This study reports the prevalence and characteristics of MVP in a large cohort of patients with UCA.
METHODS METHODS
Patients were enrolled following an UCA, defined as cardiac arrest with no coronary artery disease, preserved left ventricular ejection fraction, and no apparent explanation on electrocardiogram. A comprehensive evaluation was performed, and patients were diagnosed with idiopathic ventricular fibrillation (IVF) if no cause was found. Echocardiography reports were reviewed for MVP. Patients with MVP were divided into 2 groups: those with IVF (AMVP) and those with an alternative diagnosis (nonarrhythmic MVP). Patient characteristics were then compared. The long-term outcomes of AMVP were reported.
RESULTS RESULTS
Among 571 with an initially UCA, 34 patients had MVP (6%). The prevalence of definite MVP was significantly higher in patients with IVF than those with an alternative diagnosis (24 of 366 [6.6%] vs 5 of 205 [2.4%]; P = 0.03). Bileaflet prolapse was significantly associated with AMVP (18 of 23 [78%] vs 1 of /8 [12.5%]; P = 0.001; OR: 25.2). The proportion of patients with AMVP who received appropriate implantable cardioverter-defibrillator therapies over a median follow-up of 42 months was 21.1% (4 of 19).
CONCLUSIONS CONCLUSIONS
MVP is associated with otherwise UCA (IVF), with a prevalence of 6.6%. Bileaflet prolapse appears to be a feature of AMVP, although future studies need to ascertain its independent association. A significant proportion of patients with AMVP received appropriate implantable cardioverter-defibrillator therapies during follow-up.

Identifiants

pubmed: 37804262
pii: S2405-500X(23)00630-8
doi: 10.1016/j.jacep.2023.08.017
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Funding Support and Author Disclosures This study was supported by the Heart and Stroke Foundation of Canada (G-13-0002775 and G-14-0005732) and the Canadian Institute of Health Research (Dr Krahn, Principal Investigator, Hearts in Rhythm Organization RN380020–406814). Dr Krahn has received support from the Sauder Family and Heart and Stroke Foundation Chair in Cardiology (Vancouver, British Columbia), the Paul Brunes Chair in Heart Rhythm Disorders (Vancouver, British Columbia), and the Paul Albrechtsen Foundation (Winnipeg, Manitoba). The authors have reported that they have no relationships relevant to the contents of this paper to disclose.

Auteurs

Wael Alqarawi (W)

Department of Cardiac Sciences, College of Medicine, King Saud University, Riyadh, Saudi Arabia; Division of Cardiology, University of Ottawa Heart Institute, University of Ottawa, Ottawa, Ontario, Canada. Electronic address: walqarawi@ksu.edu.sa.

Rafik Tadros (R)

Cardiovascular Genetics Center, Montreal Heart Institute, Faculty of Medicine, Université de Montréal, Montreal, Quebec, Canada.

Jason D Roberts (JD)

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

Christopher C Cheung (CC)

Center for Cardiovascular Innovation, Division of Cardiology, University of British Columbia, Vancouver, British Columbia, Canada.

Martin S Green (MS)

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

Ian G Burwash (IG)

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

Christian Steinberg (C)

Institut Universitaire de Cardiologie et Pneumologie de Québec, Laval University, Quebec City, Quebec, Canada.

Jeffrey S Healey (JS)

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

Habib Khan (H)

Section of Cardiac Electrophysiology, Division of Cardiology, Department of Medicine, Western University, London, Ontario, Canada.

Ciorsti McIntyre (C)

Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.

Julia Cadrin-Touringy (J)

Cardiovascular Genetics Center, Montreal Heart Institute, Faculty of Medicine, Université de Montréal, Montreal, Quebec, Canada.

Zachary W M Laksman (ZWM)

Center for Cardiovascular Innovation, Division of Cardiology, University of British Columbia, Vancouver, British Columbia, Canada.

Christopher S Simpson (CS)

Cardiac Electrophysiology Service, Queen's University, Kingston, Ontario, Canada.

Shubhayan Sanatani (S)

Division of Cardiology, BC Children's Hospital, Vancouver, British Columbia, Canada.

Martin Gardner (M)

Dalhousie University and Queen Elizabeth II Health Sciences Centre, Halifax, Nova Scotia, Canada.

Paul Angaran (P)

Cardiac Arrhythmia Service, St-Michael's Hospital, Toronto, Ontario, Canada.

Erkan Ilhan (E)

Division of Cardiology, Libin Cardiovascular Institute, University of Calgary, Calgary, Alberta, Canada.

Mario Talajic (M)

Cardiovascular Genetics Center, Montreal Heart Institute, Faculty of Medicine, Université de Montréal, Montreal, Quebec, Canada.

Laura Arbour (L)

Center for Cardiovascular Innovation, Division of Cardiology, University of British Columbia, Vancouver, British Columbia, Canada.

Richard Leather (R)

Center for Cardiovascular Innovation, Division of Cardiology, University of British Columbia, Vancouver, British Columbia, Canada.

Colette Seifer (C)

St-Boniface Hospital, University of Manitoba, Winnipeg, Manitoba, Canada.

Jacqueline Joza (J)

Division of Cardiology, McGill University Health Center, Montreal, Quebec, Canada.

Felicity Lee (F)

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

Lawrence Lau (L)

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

Girish Nair (G)

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

George Wells (G)

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

Andrew D Krahn (AD)

Center for Cardiovascular Innovation, Division of Cardiology, University of British Columbia, Vancouver, British Columbia, Canada.

Classifications MeSH