Are there real benefits to implanting cardiac devices in patients with end-stage dilated dystrophinopathic cardiomyopathy? Review of literature and personal results.

Alberto Palladino, Andrea A Papa, Salvatore Morra, Vincenzo Russo, Manuela Ergoli, Anna Rago, Chiara Orsini, Gerardo Nigro, Luisa Politano
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Abstract

Cardiomyopathy associated with dystrophinopathies - Duchenne muscular Dystrophy (DMD), Becker muscular dystrophy (BMD), X-linked dilated cardiomyopathy (XL-CM) and cardiomyopathy of Duchenne/Becker (DMD/BMD carriers - is an almost constant manifestation of these neuromuscular disorders and contribute significantly to their morbidity and mortality. Dystrophinopathic cardiomyopathy is the result of the dystrophin protein deficiency at the myocardium level, parallel to that occurring at the skeletal muscle level. Typically, cardiomyopathy begins as a "presymptomatic" stage in the first decade of life and evolves in a stepwise manner toward an end-stage dilated cardiomyopathy. Nearly complete replacement of the myocardium by fibrous and fatty connective tissue results in an irreversible cardiac failure, characterized by a further reduction of ejection fraction (EF < 30%) and frequent episodes of acute heart failure (HF). The picture of a severe dilated cardiomyopathy with intractable heart failure is typical of dystrophinopathies. Despite an appropriate pharmacological treatment, this condition is irreversible because of the extensive loss of myocites. Heart transplantation is the only curative therapy for patients with end-stage heart failure, who remain symptomatic despite an optimal medical therapy. However there is a reluctance to perform heart transplantation (HT) in these patients due to the scarcity of donors and the concerns that the accompanying myopathy will limit the benefits obtained through this therapeutic option. Therefore the only possibility to ameliorate clinical symptoms, prevent fatal arrhythmias and cardiac death in dystrophinopathic patients could be the implantation of intracardiac device (ICD) or resynchronizing devices with defibrillator (CRT-D). This overview reports the personal series of patients affected by DMD and BMD and DMD carriers who received ICD or CRT-D system, describe the clinical outcomes so far published and discuss pro and cons in the use of such devices.

为终末期扩张型肌营养不良性心肌病患者植入心脏装置真的有好处吗?文献回顾与个人结果。
与肌营养不良症(杜氏肌营养不良症(DMD)、贝克尔肌营养不良症(BMD)、X-连锁扩张型心肌病(XL-CM)和杜氏/贝克尔心肌病(DMD/BMD 携带者))相关的心肌病几乎是这些神经肌肉疾病的固定表现形式,并对这些疾病的发病率和死亡率产生重大影响。肌营养不良性心肌病是心肌中肌营养不良蛋白缺乏的结果,与骨骼肌中肌营养不良蛋白缺乏的情况类似。通常情况下,心肌病开始于生命最初十年的 "无症状 "阶段,然后逐步演变为终末期扩张型心肌病。纤维和脂肪结缔组织几乎完全取代了心肌,导致不可逆的心力衰竭,其特点是射血分数进一步降低(EF < 30%),急性心力衰竭(HF)频繁发作。严重的扩张型心肌病伴有顽固性心力衰竭是肌营养不良症的典型表现。尽管采取了适当的药物治疗,但由于肌细胞的大量丧失,这种病症是不可逆的。心脏移植是治疗终末期心力衰竭患者的唯一方法。然而,由于供体稀缺,以及担心伴随的肌病会限制通过这种治疗方法获得的益处,人们不愿意为这些患者进行心脏移植(HT)。因此,改善肌营养不良症患者的临床症状、预防致命性心律失常和心源性死亡的唯一可能就是植入心内装置(ICD)或带除颤器的再同步装置(CRT-D)。本综述报告了接受 ICD 或 CRT-D 系统治疗的 DMD 和 BMD 患者以及 DMD 携带者的个人系列,描述了迄今为止发表的临床结果,并讨论了使用此类装置的利弊。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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