Management of sudden cardiac death in cardiac sarcoidosis using the wearable cardioverter defibrillator.

Patients with cardiac sarcoidosis are at increased risk of ventricular tachycardia/fibrillation.We tested the hypothesis that the wearable cardioverter defibrillator can be used to mitigate the risk of sudden cardiac death among cardiac sarcoidosis patients.A retrospective review of the commercial d...

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Main Authors: Dirk Skowasch, Steven Ringquist, Georg Nickenig, René Andrié
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5864098?pdf=render
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author Dirk Skowasch
Steven Ringquist
Georg Nickenig
René Andrié
author_facet Dirk Skowasch
Steven Ringquist
Georg Nickenig
René Andrié
author_sort Dirk Skowasch
collection DOAJ
description Patients with cardiac sarcoidosis are at increased risk of ventricular tachycardia/fibrillation.We tested the hypothesis that the wearable cardioverter defibrillator can be used to mitigate the risk of sudden cardiac death among cardiac sarcoidosis patients.A retrospective review of the commercial database identified cardiac sarcoidosis patients who wore the wearable cardioverter defibrillator. Evidence for cardiac sarcoidosis diagnosis as well as demographic, co-morbidity and left ventricular ejection fraction were provided by patient clinical records. Clinical data also included daily wearable cardioverter defibrillator wear, shock treatment and survival information.The wearable cardioverter defibrillator was worn by 46 cardiac sarcoidosis patients, 24 (52%) male. The median age was 48 years and median left ventricular ejection fraction was 30%. The wearable cardioverter defibrillator was worn a median of 23.6 hours each day. There were 11 ventricular tachycardia/fibrillation episodes occurring in 10 (22%) patients. Ventricular tachycardia/fibrillation occurred over a range of 1 to 79 days, median 24 days. First-shock success for conversion of ventricular tachycardia/fibrillation was 100%. Patient survival 24 hours after shock treatment was 100%. Follow up to determine the reason for discontinuing wearable cardioverter defibrillator use indicated that among shocked patients 7 received an implantable cardioverter defibrillator, 1 patient was admitted to the hospital ending in death 2 weeks after discontinuing wearable cardioverter defibrillator use, and 2 patients were lost to follow up. Among the not shocked patients, there were 16 who received an implantable cardioverter defibrillator while 7 achieved improved left ventricular ejection fraction.Management of sudden cardiac death among cardiac sarcoidosis patients was aided by the wearable cardioverter defibrillator resulting in successful termination of ventricular tachycardia/fibrillation upon delivery of shock.
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spelling doaj.art-2525a54ac4d34d44a8bd21a6c89188e52022-12-21T17:56:43ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-01133e019449610.1371/journal.pone.0194496Management of sudden cardiac death in cardiac sarcoidosis using the wearable cardioverter defibrillator.Dirk SkowaschSteven RingquistGeorg NickenigRené AndriéPatients with cardiac sarcoidosis are at increased risk of ventricular tachycardia/fibrillation.We tested the hypothesis that the wearable cardioverter defibrillator can be used to mitigate the risk of sudden cardiac death among cardiac sarcoidosis patients.A retrospective review of the commercial database identified cardiac sarcoidosis patients who wore the wearable cardioverter defibrillator. Evidence for cardiac sarcoidosis diagnosis as well as demographic, co-morbidity and left ventricular ejection fraction were provided by patient clinical records. Clinical data also included daily wearable cardioverter defibrillator wear, shock treatment and survival information.The wearable cardioverter defibrillator was worn by 46 cardiac sarcoidosis patients, 24 (52%) male. The median age was 48 years and median left ventricular ejection fraction was 30%. The wearable cardioverter defibrillator was worn a median of 23.6 hours each day. There were 11 ventricular tachycardia/fibrillation episodes occurring in 10 (22%) patients. Ventricular tachycardia/fibrillation occurred over a range of 1 to 79 days, median 24 days. First-shock success for conversion of ventricular tachycardia/fibrillation was 100%. Patient survival 24 hours after shock treatment was 100%. Follow up to determine the reason for discontinuing wearable cardioverter defibrillator use indicated that among shocked patients 7 received an implantable cardioverter defibrillator, 1 patient was admitted to the hospital ending in death 2 weeks after discontinuing wearable cardioverter defibrillator use, and 2 patients were lost to follow up. Among the not shocked patients, there were 16 who received an implantable cardioverter defibrillator while 7 achieved improved left ventricular ejection fraction.Management of sudden cardiac death among cardiac sarcoidosis patients was aided by the wearable cardioverter defibrillator resulting in successful termination of ventricular tachycardia/fibrillation upon delivery of shock.http://europepmc.org/articles/PMC5864098?pdf=render
spellingShingle Dirk Skowasch
Steven Ringquist
Georg Nickenig
René Andrié
Management of sudden cardiac death in cardiac sarcoidosis using the wearable cardioverter defibrillator.
PLoS ONE
title Management of sudden cardiac death in cardiac sarcoidosis using the wearable cardioverter defibrillator.
title_full Management of sudden cardiac death in cardiac sarcoidosis using the wearable cardioverter defibrillator.
title_fullStr Management of sudden cardiac death in cardiac sarcoidosis using the wearable cardioverter defibrillator.
title_full_unstemmed Management of sudden cardiac death in cardiac sarcoidosis using the wearable cardioverter defibrillator.
title_short Management of sudden cardiac death in cardiac sarcoidosis using the wearable cardioverter defibrillator.
title_sort management of sudden cardiac death in cardiac sarcoidosis using the wearable cardioverter defibrillator
url http://europepmc.org/articles/PMC5864098?pdf=render
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