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Long‐term support by left ventricular assist device for arrhythmogenic right ventricular cardiomyopathy
Author(s) -
Minegishi Sachito,
Kinoshita Osamu,
Hoshino Yasuhiro,
Komae Hyoe,
Kimura Mitsutoshi,
Shimada Shogo,
Yamauchi Haruo,
Nawata Kan,
Ono Minoru
Publication year - 2019
Publication title -
artificial organs
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.684
H-Index - 76
eISSN - 1525-1594
pISSN - 0160-564X
DOI - 10.1111/aor.13482
Subject(s) - medicine , cardiology , ventricular assist device , context (archaeology) , heart failure , cardiomyopathy , arrhythmogenic right ventricular dysplasia , heart transplantation , sudden cardiac death , paleontology , biology
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heart muscle disorder characterized by right ventricular enlargement, right heart failure (HF), and ventricular arrhythmias which lead to sudden death especially in young adults. Current recommendations for management of patients with ARVC are antiarrhythmic medications, catheter ablation, and implantable cardioverter defibrillator therapy to prevent sudden cardiac death. However, despite these treatments, few patients suffer from recurrent ventricular arrhythmias or HF unresponsive to conventional management. Heart transplantation (HTx) is a preferred treatment for these cases, but because of a persistent donor heart shortage in Japan, ventricular assist device (VAD) support has become an important option for a management of the end‐stage ARVC. Previous articles reported 4 cases of a successful management by left ventricular assist device (LVAD), but the longest interval of LVAD support was only 333 days. We present 3 cases of ARVC patients who were successfully managed by LVAD implantation for more than a year. These 3 cases are unconventional examples of ARVC patients, considering the nature of the disease. The novelty of these cases should be taken in the context of the extremely long waiting period for HTx in Japan.