Arrhythmic Prognosis According to Left Ventricular Systolic Dysfunction Severity in Cardiac Sarcoidosis.

cardiac sarcoidosis cardiovascular implantable electronic device heart failure sudden cardiac death ventricular arrhythmia

Journal

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

Informations de publication

Date de publication:
27 Aug 2024
Historique:
received: 24 05 2024
revised: 19 08 2024
accepted: 22 08 2024
medline: 31 8 2024
pubmed: 31 8 2024
entrez: 29 8 2024
Statut: aheadofprint

Résumé

Current guidelines present varying classes of recommendations for implantable cardioverter-defibrillator (ICD) utilization in patients with cardiac sarcoidosis (CS) and left ventricular ejection fraction (LVEF) <50%. To investigate the ventricular arrhythmia risk in CS patients with ICDs and varying degrees of LV systolic dysfunction. We included CS patients with an ICD and LVEF <50% at index evaluation. The primary outcome was survival free of sustained ventricular tachycardia/fibrillation (VT/VF) after ICD implantation and was assessed comparatively for LVEF ≤35 vs 36-49% and for primary vs secondary prevention ICD indication. We included 61 patients (median age 57 years, 61% male) with LVEF 36-49% (n=23) or LVEF ≤35% (n=38). An ICD was implanted for secondary prevention in 24% and 44% of the LVEF ≤35% and 36-49% groups, respectively (p=0.11). The primary outcome did not differ between the two groups in univariable analysis (LVEF ≤35% vs 36-49% HR 0.85 [95% CI 0.39, 1.82], p=0.67). In multivariable analysis, secondary prevention ICD indication was the only significant predictor of incident sustained VT/VF (HR 2.86 [95% CI 1.23, 6.67], p=0.015). The mean sustained VT/VF event burden was higher in the secondary as compared with the primary prevention ICD patients (0.47 vs 0.11 events/patient-year, p=0.005) but did not differ significantly between LVEF ≤35% and 36-49% patients. CS patients with ICD indications and LVEF 36-49% carry similarly high arrhythmic risk as those with LVEF ≤35%. Patients with secondary prevention ICDs have the highest overall risk.

Sections du résumé

BACKGROUND BACKGROUND
Current guidelines present varying classes of recommendations for implantable cardioverter-defibrillator (ICD) utilization in patients with cardiac sarcoidosis (CS) and left ventricular ejection fraction (LVEF) <50%.
OBJECTIVE OBJECTIVE
To investigate the ventricular arrhythmia risk in CS patients with ICDs and varying degrees of LV systolic dysfunction.
METHODS METHODS
We included CS patients with an ICD and LVEF <50% at index evaluation. The primary outcome was survival free of sustained ventricular tachycardia/fibrillation (VT/VF) after ICD implantation and was assessed comparatively for LVEF ≤35 vs 36-49% and for primary vs secondary prevention ICD indication.
RESULTS RESULTS
We included 61 patients (median age 57 years, 61% male) with LVEF 36-49% (n=23) or LVEF ≤35% (n=38). An ICD was implanted for secondary prevention in 24% and 44% of the LVEF ≤35% and 36-49% groups, respectively (p=0.11). The primary outcome did not differ between the two groups in univariable analysis (LVEF ≤35% vs 36-49% HR 0.85 [95% CI 0.39, 1.82], p=0.67). In multivariable analysis, secondary prevention ICD indication was the only significant predictor of incident sustained VT/VF (HR 2.86 [95% CI 1.23, 6.67], p=0.015). The mean sustained VT/VF event burden was higher in the secondary as compared with the primary prevention ICD patients (0.47 vs 0.11 events/patient-year, p=0.005) but did not differ significantly between LVEF ≤35% and 36-49% patients.
CONCLUSIONS CONCLUSIONS
CS patients with ICD indications and LVEF 36-49% carry similarly high arrhythmic risk as those with LVEF ≤35%. Patients with secondary prevention ICDs have the highest overall risk.

Identifiants

pubmed: 39209225
pii: S1547-5271(24)03267-3
doi: 10.1016/j.hrthm.2024.08.049
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Auteurs

B Michelle Kim (BM)

Mayo Clinic Alix School of Medicine, Mayo Clinic, Rochester, MN.

Daniel Sykora (D)

Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN.

Andrew N Rosenbaum (AN)

Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN.

Enas Ahmed (E)

Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN.

Robert A Churchill (RA)

Mayo Clinic Alix School of Medicine, Mayo Clinic, Rochester, MN.

Melanie Bratcher (M)

Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN.

Mohamed Y Elwazir (MY)

Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN.

John P Bois (JP)

Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN.

John R Giudicessi (JR)

Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN.

Alan M Sugrue (AM)

Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN.

Ammar M Killu (AM)

Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN.

Suraj Kapa (S)

Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN.

Abhishek J Deshmukh (AJ)

Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN.

Samuel J Asirvatham (SJ)

Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN.

Leslie T Cooper (LT)

Department of Cardiovascular Medicine, Mayo Clinic, Jacksonville, FL.

Omar F Abou Ezzeddine (OF)

Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN.

Konstantinos C Siontis (KC)

Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN. Electronic address: Siontis.Konstantinos@mayo.edu.

Classifications MeSH