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Outcomes after transvenous defibrillator implantation in cardiac sarcoidosis: A systematic review

INTRODUCTION: Sarcoidosis is a systemic inflammatory disorder associated with ventricular arrhythmias (VAs) and sudden death in the context of cardiac involvement. Guidelines advocate implantable cardioverter‐defibrillator (ICD) implantation in specific subcohorts, but there is a paucity of data on...

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Autores principales: Taha, Ahmed, Assaf, Omar, Champsi, Asgher, Nadarajah, Ramesh, Patel, Peysh A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9535799/
https://www.ncbi.nlm.nih.gov/pubmed/36237869
http://dx.doi.org/10.1002/joa3.12753
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author Taha, Ahmed
Assaf, Omar
Champsi, Asgher
Nadarajah, Ramesh
Patel, Peysh A.
author_facet Taha, Ahmed
Assaf, Omar
Champsi, Asgher
Nadarajah, Ramesh
Patel, Peysh A.
author_sort Taha, Ahmed
collection PubMed
description INTRODUCTION: Sarcoidosis is a systemic inflammatory disorder associated with ventricular arrhythmias (VAs) and sudden death in the context of cardiac involvement. Guidelines advocate implantable cardioverter‐defibrillator (ICD) implantation in specific subcohorts, but there is a paucity of data on outcomes. METHODS AND RESULTS: A systematic review was performed to assess outcomes in patients with definite or probable cardiac sarcoidosis (CS) treated with ICD. Observational studies were identified from multiple databases from inception to 21st May 2021. Outcomes of interest included appropriate and inappropriate ICD therapies in addition to all‐cause mortality. Study quality was assessed individually using the Newcastle Ottawa Scale (NOS). Eight studies were identified comprising 530 patients, with follow‐up period of 24–66 months (weighted average 40 months). Mean age was 53.9 years with ejection fraction of 41.3%. Overall incidence of appropriate therapy was 38.1% during follow‐up. Left ventricular systolic dysfunction (LVSD) with ejection fraction <40% was a predictor of appropriate therapy in the majority of studies, as were sustained VAs during electrophysiological testing (EP) in one study. There was no interaction with device indication (i.e. primary or secondary). Where documented, inappropriate therapy was primarily driven by atrial arrhythmias. All‐cause mortality was 6.0% over a median follow‐up period of 42 months. Only three studies achieved good quality in the comparability domain of NOS. CONCLUSIONS: Appropriate ICD therapy in patients with CS is commonly associated with LVSD, which can act as a surrogate for scar burden. The utility of EP testing in this setting remains unclear.
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spelling pubmed-95357992022-10-12 Outcomes after transvenous defibrillator implantation in cardiac sarcoidosis: A systematic review Taha, Ahmed Assaf, Omar Champsi, Asgher Nadarajah, Ramesh Patel, Peysh A. J Arrhythm Original Articles INTRODUCTION: Sarcoidosis is a systemic inflammatory disorder associated with ventricular arrhythmias (VAs) and sudden death in the context of cardiac involvement. Guidelines advocate implantable cardioverter‐defibrillator (ICD) implantation in specific subcohorts, but there is a paucity of data on outcomes. METHODS AND RESULTS: A systematic review was performed to assess outcomes in patients with definite or probable cardiac sarcoidosis (CS) treated with ICD. Observational studies were identified from multiple databases from inception to 21st May 2021. Outcomes of interest included appropriate and inappropriate ICD therapies in addition to all‐cause mortality. Study quality was assessed individually using the Newcastle Ottawa Scale (NOS). Eight studies were identified comprising 530 patients, with follow‐up period of 24–66 months (weighted average 40 months). Mean age was 53.9 years with ejection fraction of 41.3%. Overall incidence of appropriate therapy was 38.1% during follow‐up. Left ventricular systolic dysfunction (LVSD) with ejection fraction <40% was a predictor of appropriate therapy in the majority of studies, as were sustained VAs during electrophysiological testing (EP) in one study. There was no interaction with device indication (i.e. primary or secondary). Where documented, inappropriate therapy was primarily driven by atrial arrhythmias. All‐cause mortality was 6.0% over a median follow‐up period of 42 months. Only three studies achieved good quality in the comparability domain of NOS. CONCLUSIONS: Appropriate ICD therapy in patients with CS is commonly associated with LVSD, which can act as a surrogate for scar burden. The utility of EP testing in this setting remains unclear. John Wiley and Sons Inc. 2022-07-23 /pmc/articles/PMC9535799/ /pubmed/36237869 http://dx.doi.org/10.1002/joa3.12753 Text en © 2022 The Authors. Journal of Arrhythmia published by John Wiley & Sons Australia, Ltd on behalf of Japanese Heart Rhythm Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Taha, Ahmed
Assaf, Omar
Champsi, Asgher
Nadarajah, Ramesh
Patel, Peysh A.
Outcomes after transvenous defibrillator implantation in cardiac sarcoidosis: A systematic review
title Outcomes after transvenous defibrillator implantation in cardiac sarcoidosis: A systematic review
title_full Outcomes after transvenous defibrillator implantation in cardiac sarcoidosis: A systematic review
title_fullStr Outcomes after transvenous defibrillator implantation in cardiac sarcoidosis: A systematic review
title_full_unstemmed Outcomes after transvenous defibrillator implantation in cardiac sarcoidosis: A systematic review
title_short Outcomes after transvenous defibrillator implantation in cardiac sarcoidosis: A systematic review
title_sort outcomes after transvenous defibrillator implantation in cardiac sarcoidosis: a systematic review
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9535799/
https://www.ncbi.nlm.nih.gov/pubmed/36237869
http://dx.doi.org/10.1002/joa3.12753
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