Choudhry Swati, Puri Kriti, Denfield Susan W
Department of Pediatrics, Section of Pediatric Cardiology, Texas Children's Hospital, Baylor College of Medicine, 6651 Main St, Houston, TX, 77030, USA.
Curr Treat Options Cardiovasc Med. 2019 Jun 25;21(8):36. doi: 10.1007/s11936-019-0739-y.
This review summarizes the clinical characteristics and updated outcomes of primary pediatric cardiomyopathies including dilated (DCM), hypertrophic (HCM), and restrictive cardiomyopathy (RCM), and briefly discusses left ventricular non-compaction (LVNC) and arrhythmogenic cardiomyopathy (ACM), primarily arrythmogenic right ventricular cardiomyopathy (ARVC).
Pediatric cardiomyopathies are diseases of the heart muscle with an estimated annual incidence of 1.1-1.5 cases per 100,000. They are progressive in nature and are frequently caused by a genetic mutation causing a structural abnormality in the myocyte. Dilated cardiomyopathy, characterized by left ventricular dilation and systolic dysfunction with normal left ventricular wall thickness, accounts for about 50-60% of all pediatric cardiomyopathy cases. This is followed by hypertrophic cardiomyopathy accounting for about 40%, characterized by abnormally thickened myocardium in the absence of another cause of hypertrophy with non-dilated left ventricle. Left ventricular non-compaction and restrictive cardiomyopathy each account for about 5% of the cases. Genetic mutations play a dominant role in the development of pediatric cardiomyopathies. While treatment for congestive heart failure and arrhythmias alleviates symptoms, it has not been shown to reduce the risk of sudden death. The 5-year transplant-free survival of DCM, HCM, RCM, and LVNC are 50%, 90%, 30%, and 60% respectively. Pediatric cardiomyopathies while not common they are a significant cause of morbidity and mortality in afflicted children. Dilated forms are the most common followed by hypertrophic, left ventricular non-compaction, and restrictive cardiomyopathies. Arrhythmogenic cardiomyopathies tend to be diagnosed later in the teenage years. Treatment typically follows adult recommendations for which there is significantly more data on treatment benefits, although the indications for ICD placement in children remain even less clear, other than for secondary prevention.
本综述总结了原发性小儿心肌病的临床特征和最新转归,包括扩张型心肌病(DCM)、肥厚型心肌病(HCM)和限制型心肌病(RCM),并简要讨论了左心室心肌致密化不全(LVNC)和致心律失常性心肌病(ACM),主要是致心律失常性右心室心肌病(ARVC)。
小儿心肌病是一种心肌疾病,估计年发病率为每10万人中有1.1 - 1.5例。其本质上具有进行性,常由导致心肌细胞结构异常的基因突变引起。扩张型心肌病的特征是左心室扩张和收缩功能障碍,左心室壁厚度正常,约占所有小儿心肌病病例的50 - 60%。其次是肥厚型心肌病,约占40%,其特征是在无其他肥厚原因且左心室未扩张的情况下心肌异常增厚。左心室心肌致密化不全和限制型心肌病各占病例的约5%。基因突变在小儿心肌病的发生发展中起主导作用。虽然针对充血性心力衰竭和心律失常的治疗可缓解症状,但尚未证明能降低猝死风险。DCM、HCM、RCM和LVNC的5年无移植生存率分别为50%、90%、30%和60%。小儿心肌病虽不常见,但却是患病儿童发病和死亡的重要原因。扩张型最为常见,其次是肥厚型、左心室心肌致密化不全和限制型心肌病。致心律失常性心肌病往往在青少年后期才被诊断出来。治疗通常遵循成人的建议,关于治疗益处的数据更多,尽管除二级预防外,儿童植入式心律转复除颤器(ICD)的植入指征仍不明确。