Predicting sustained ventricular arrhythmias in dilated cardiomyopathy: a meta-analysis and systematic review.


Journal

ESC heart failure
ISSN: 2055-5822
Titre abrégé: ESC Heart Fail
Pays: England
ID NLM: 101669191

Informations de publication

Date de publication:
08 2020
Historique:
received: 22 10 2019
revised: 07 01 2020
accepted: 11 03 2020
pubmed: 15 4 2020
medline: 22 6 2021
entrez: 15 4 2020
Statut: ppublish

Résumé

Patients with non-ischaemic dilated cardiomyopathy (DCM) are at increased risk of sudden cardiac death. Identification of patients that may benefit from implantable cardioverter-defibrillator implantation remains challenging. In this study, we aimed to determine predictors of sustained ventricular arrhythmias in patients with DCM. We searched MEDLINE/Embase for studies describing predictors of sustained ventricular arrhythmias in patients with DCM. Quality and bias were assessed using the Quality in Prognostic Studies tool, articles with high risk of bias in ≥2 areas were excluded. Unadjusted hazard ratios (HRs) of uniformly defined predictors were pooled, while all other predictors were evaluated in a systematic review. We included 55 studies (11 451 patients and 3.7 ± 2.3 years follow-up). Crude annual event rate was 4.5%. Younger age [HR 0.82; 95% CI (0.74-1.00)], hypertension [HR 1.95; 95% CI (1.26-3.00)], prior sustained ventricular arrhythmia [HR 4.15; 95% CI (1.32-13.02)], left ventricular ejection fraction on ultrasound [HR 1.45; 95% CI (1.19-1.78)], left ventricular dilatation (HR 1.10), and presence of late gadolinium enhancement [HR 5.55; 95% CI (4.02-7.67)] were associated with arrhythmic outcome in pooled analyses. Prior non-sustained ventricular arrhythmia and several genotypes [mutations in Phospholamban (PLN), Lamin A/C (LMNA), and Filamin-C (FLNC)] were associated with arrhythmic outcome in non-pooled analyses. Quality of evidence was moderate, and heterogeneity among studies was moderate to high. In patients with DCM, the annual event rate of sustained ventricular arrhythmias is approximately 4.5%. This risk is considerably higher in younger patients with hypertension, prior (non-)sustained ventricular arrhythmia, decreased left ventricular ejection fraction, left ventricular dilatation, late gadolinium enhancement, and genetic mutations (PLN, LMNA, and FLNC). These results may help determine appropriate candidates for implantable cardioverter-defibrillator implantation.

Identifiants

pubmed: 32285648
doi: 10.1002/ehf2.12689
pmc: PMC7373946
doi:

Substances chimiques

Contrast Media 0
Gadolinium AU0V1LM3JT

Types de publication

Journal Article Meta-Analysis Research Support, Non-U.S. Gov't Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1430-1441

Subventions

Organisme : UCL Hospitals NIHR Biomedical Research
Pays : International
Organisme : German Centre for Cardiovascular Research, DZHK
ID : 81X3500117
Pays : International
Organisme : CVON 2015-12 eDETECT
Pays : International
Organisme : UMC Utrecht Fellowship Clinical Research Talent
Pays : International
Organisme : Alexandre Suerman Stipendium
Pays : International
Organisme : Netherlands Organization for Health Research and Development
Pays : International
Organisme : Dutch Heart Foundation
ID : 2015T058
Pays : International
Organisme : Dutch Heart Foundation
ID : 2016T096
Pays : International
Organisme : European Union's Horizon 2020
ID : 680969
Pays : International

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2020 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of the European Society of Cardiology.

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Auteurs

Arjan Sammani (A)

Department of Cardiology, Division Heart & Lungs, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.

Elham Kayvanpour (E)

Department of Cardiology, University Hospital of Heidelberg, INF 410, 69120, Heidelberg, Germany.
DZHK (German Centre for Cardiovascular Research), Berlin, Germany.

Laurens P Bosman (LP)

Department of Cardiology, Division Heart & Lungs, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.

Farbod Sedaghat-Hamedani (F)

Department of Cardiology, University Hospital of Heidelberg, INF 410, 69120, Heidelberg, Germany.
DZHK (German Centre for Cardiovascular Research), Berlin, Germany.

Tanja Proctor (T)

Institute of Medical Biometry and Informatics, University of Heidelberg, Heidelberg, Germany.

Weng-Tein Gi (WT)

Department of Cardiology, University Hospital of Heidelberg, INF 410, 69120, Heidelberg, Germany.
DZHK (German Centre for Cardiovascular Research), Berlin, Germany.

Alicia Broezel (A)

Department of Cardiology, University Hospital of Heidelberg, INF 410, 69120, Heidelberg, Germany.
DZHK (German Centre for Cardiovascular Research), Berlin, Germany.

Katrin Jensen (K)

Institute of Medical Biometry and Informatics, University of Heidelberg, Heidelberg, Germany.

Hugo A Katus (HA)

Department of Cardiology, University Hospital of Heidelberg, INF 410, 69120, Heidelberg, Germany.
DZHK (German Centre for Cardiovascular Research), Berlin, Germany.

Anneline S J M Te Riele (ASJM)

Department of Cardiology, Division Heart & Lungs, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.

Benjamin Meder (B)

Department of Cardiology, University Hospital of Heidelberg, INF 410, 69120, Heidelberg, Germany.
DZHK (German Centre for Cardiovascular Research), Berlin, Germany.
Department of Genetics, Stanford Genome Technology Center, Stanford University School of Medicine, Stanford, CA, USA.

Folkert W Asselbergs (FW)

Department of Cardiology, Division Heart & Lungs, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
Institute of Cardiovascular Science, Faculty of Population Health Sciences, University College London, London, UK.
Health Data Research UK and Institute of Health Informatics, University College London, London, UK.

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