Implantable cardioverter defibrillators in patients with orthotopic heart transplant: A multicenter case series.


Journal

Journal of cardiovascular electrophysiology
ISSN: 1540-8167
Titre abrégé: J Cardiovasc Electrophysiol
Pays: United States
ID NLM: 9010756

Informations de publication

Date de publication:
08 2022
Historique:
revised: 11 05 2022
received: 21 03 2022
accepted: 19 05 2022
pubmed: 8 6 2022
medline: 24 8 2022
entrez: 7 6 2022
Statut: ppublish

Résumé

Sudden cardiac death (SCD) is common after orthotopic heart transplant (OHT). No clear guidelines for implantable cardioverter defibrillator (ICD) implantation in OHT patients at high risk for SCD currently exist. To assess the safety, efficacy, and benefit of ICDs and resynchronization therapy post-OHT. We also provide a systematic review of previous reports. A retrospective multicenter cohort study within the United States. Patients with ICD post-OHT between 2000 and 2020 were identified. We analyzed 16 patients from 4 centers. The mean standard-deviation (SD) age was 43 (18) years at OHT and 51 (20) years at ICD implantation. The mean (SD) duration from OHT to ICD implantation was 9 (5) years. The mean (SD) left ventricular ejection fraction (LVEF) was 35% (17%). There were 2 (13%) postprocedural complications: 1 hematoma and 1 death. Mean (SD) follow-up was 24 (23) months. Survival rate was 63% (10/16) at 1 year and 56% (9/16) at 2 years, with 6/7 of those who died having LVEF < 35% at the time of the ICD implantation. Patients were more likely to receive appropriate therapy if their ICD was implanted for secondary (5/8) rather than primary (0/8) prevention (p = .007). Of those who did, 4 patients survived to 30 days post-ICD therapy. Severe CAV was not associated with the rate of appropriate therapy. Beneficial outcomes were observed when ICDs were implanted for secondary prevention only, and in patients with higher baseline LVEF. We also observed benefits with resynchronization therapy.

Sections du résumé

BACKGROUND
Sudden cardiac death (SCD) is common after orthotopic heart transplant (OHT). No clear guidelines for implantable cardioverter defibrillator (ICD) implantation in OHT patients at high risk for SCD currently exist.
OBJECTIVES
To assess the safety, efficacy, and benefit of ICDs and resynchronization therapy post-OHT. We also provide a systematic review of previous reports.
METHODS
A retrospective multicenter cohort study within the United States. Patients with ICD post-OHT between 2000 and 2020 were identified.
RESULTS
We analyzed 16 patients from 4 centers. The mean standard-deviation (SD) age was 43 (18) years at OHT and 51 (20) years at ICD implantation. The mean (SD) duration from OHT to ICD implantation was 9 (5) years. The mean (SD) left ventricular ejection fraction (LVEF) was 35% (17%). There were 2 (13%) postprocedural complications: 1 hematoma and 1 death. Mean (SD) follow-up was 24 (23) months. Survival rate was 63% (10/16) at 1 year and 56% (9/16) at 2 years, with 6/7 of those who died having LVEF < 35% at the time of the ICD implantation. Patients were more likely to receive appropriate therapy if their ICD was implanted for secondary (5/8) rather than primary (0/8) prevention (p = .007). Of those who did, 4 patients survived to 30 days post-ICD therapy. Severe CAV was not associated with the rate of appropriate therapy.
CONCLUSIONS
Beneficial outcomes were observed when ICDs were implanted for secondary prevention only, and in patients with higher baseline LVEF. We also observed benefits with resynchronization therapy.

Identifiants

pubmed: 35671363
doi: 10.1111/jce.15588
doi:

Types de publication

Journal Article Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1813-1822

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2022 Wiley Periodicals LLC.

Références

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Auteurs

Waddah Maskoun (W)

Division of Electrophysiology, Department of Cardiovascular Diseases, Henry Ford Health System, Detroit, Michigan, USA.

Mohamad Raad (M)

Division of Electrophysiology, Department of Cardiovascular Diseases, Henry Ford Health System, Detroit, Michigan, USA.

Yong-Mei Cha (YM)

Division of Electrophysiology, Department of Cardiovascular Diseases, Mayo Clinic, Rochester, Minnesota, USA.

Mahmoud Houmsse (M)

Division of Electrophysiology, Department of Cardiovascular Diseases, Ohio State University, Columbus, Ohio, USA.

Amjad Abualsuod (A)

Division of Cardiology, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.

Fatima Ezzeddine (F)

Division of Electrophysiology, Department of Cardiovascular Diseases, Mayo Clinic, Rochester, Minnesota, USA.

Justin Pieper (J)

Division of Electrophysiology, Department of Cardiovascular Diseases, Ohio State University, Columbus, Ohio, USA.

Khaled Jamoor (K)

Division of Electrophysiology, Department of Cardiovascular Diseases, Henry Ford Health System, Detroit, Michigan, USA.

Cristina Tita (C)

Division of Advanced Heart Failure and Transplant Cardiology, Department of Cardiovascular Diseases, Henry Ford Health System, Detroit, Michigan, USA.

John Miller (J)

Division of Cardiology, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.

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