婴儿期特发性扩张型心肌病:“冬季雾蒙蒙的路”

Debasish Das, A. Banerjee, Tutan Das, S. Singh, J. Gupta, Subhash R. Pramanik
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引用次数: 0

摘要

扩张型心肌病,当诊断在婴儿期,提出了一系列的困难,从达到病因诊断到预后的长期结果。在这里,我们报告了一个6个月大的特发性扩张型心肌病患儿,他对最佳剂量的卡维地洛-受体阻滞剂反应良好,6个月后心脏重塑良好,射血分数(EF)显著改善(EF为22-44%),儿童症状显著改善。我们的病例提供了一个独特的信息,即在治疗婴儿期特发性扩张型心肌病(DCM)时,优化β受体阻滞剂的使用通常是清除特发性DCM模糊道路并获得良好结果的唯一途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Idiopathic dilated cardiomyopathy as cor bovinum in infancy: “A foggy road in winter”
Dilated cardiomyopathy, when diagnosed in infancy, poses an array of difficulties from reaching an etiological diagnosis to prognosticating the long-term outcome. Here, we report a case of idiopathic dilated cardiomyopathy in a 6-month-old child who responded well to beta-blocker (Carvedilol) in optimum dosage and revealed favorable cardiac remodeling over 6 months with substantial improvement in ejection fraction (EF) (EF of 22–44%) with significant amelioration of child’s symptoms. Our case has a unique message that while treating idiopathic dilated cardiomyopathy (DCM) in infancy, optimized use of the beta-blockers is most often the only way to clear the foggy road of idiopathic DCM and obtain a favorable outcome.
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