Manchester Heart Centre/Institute of Cardiovascular Medicine; Centre for Genetic Medicine, Institute of Human Development, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.
J Cardiovasc Electrophysiol. 2013 Sep;24(9):1051-3. doi: 10.1111/jce.12142. Epub 2013 Apr 11.
Danon disease is a rare X-linked lysosomal disease causing severe hypertrophic cardiomyopathy (LAMP2 cardiomyopathy) and an extremely poor prognosis in males, with several reported cases of sudden cardiac death despite the use of transvenous implantable cardioverter defibrillators (TV-ICD). We describe a case in which a TV-ICD was unable to defibrillate induced ventricular fibrillation (VF), but a wholly subcutaneous system (S-ICD) was successful in terminating induced VF and spontaneous ventricular tachycardia. These findings have relevance to the selection of device therapy in the management of these individuals and a wider group of young patients with severe hypertrophic cardiomyopathy.
丹农病是一种罕见的 X 连锁溶酶体疾病,导致严重的肥厚型心肌病(LAMP2 心肌病),男性预后极差,尽管使用了经静脉植入式心脏复律除颤器(TV-ICD),但已有数例报道心脏性猝死。我们描述了一例 TV-ICD 无法除颤诱发的心室颤动(VF),但完全皮下系统(S-ICD)成功终止了诱发的 VF 和自发性室性心动过速。这些发现与这些个体以及更广泛的患有严重肥厚型心肌病的年轻患者的装置治疗选择有关。