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

机译:在末期扩张型肌营养不良性心肌病患者中植入心脏装置是否有真正的益处?评论文学和个人成果

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摘要

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.
机译:与肌营养不良症相关的心肌病–杜兴氏肌营养不良(DMD),贝克尔肌营养不良(BMD),X连锁扩张型心肌病(XL-CM)和杜兴氏/贝克病(DMD / BMD携带者)–是这些神经肌肉疾病的几乎恒定表现。肌营养不良性心肌病是心肌水平的肌营养不良蛋白缺乏症的结果,与骨骼肌水平的肌营养不良症有关,典型地,心肌病开始于生命的前十年的“症状前”阶段。并逐步发展为终末期扩张型心肌病。纤维和脂肪结缔组织几乎完全替代心肌会导致不可逆的心力衰竭,其特征在于射血分数进一步降低(EF <30%)和频繁发作急性心力衰竭(HF)的照片。严重扩张型心肌病伴顽固性心脏病失败是典型的营养不良症。尽管进行了适当的药理学治疗,但由于肌成纤维细胞大量流失,这种情况是不可逆的。心脏移植是终末期心力衰竭患者的唯一治疗方法,尽管采用了最佳药物治疗,但仍对症治疗。然而,由于捐赠者的匮乏,以及由于伴随的肌病会限制通过这种治疗方法获得的益处,这些患者不愿进行心脏移植(HT)。因此,改善营养不良患者的临床症状,预防致命性心律失常和心脏死亡的唯一可能方法是植入心内装置(ICD)或使用除颤器再同步装置(CRT-D)。此概述报告了接受ICD或CRT-D系统治疗,受DMD和BMD和DMD携带者影响的患者个人系列,描述了迄今为止发表的临床结果,并讨论了使用此类设备的利弊。

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