肥厚性心肌病

P. Charron (Maître de conférences des Universités, praticien hospitalier), M. Komajda (Professeur des Universités, praticien hospitalier)
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引用次数: 0

摘要

肥厚型心肌病的特点是左心室不对称肥大,尤其是室间隔。25%的病例出现左心室流出梯度。这种疾病通常是遗传性的,导致这种疾病的基因编码肌节蛋白。自然病程通常是有利的,但有时可能会出现并发症,如猝死或充血性心力衰竭。治疗仍然很困难。如果β受体阻滞剂或维拉帕米不能控制症状,并且存在压力梯度,则可以建议进行肌切开髓鞘切除术。这种情况下的其他治疗方法是双腔起搏或非手术隔膜复位(酒精注射)。对于猝死高危患者,可以建议使用胺碘酮或植入式心律转复除颤器。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cardiomyopathie hypertrophique

Hypertrophic cardiomyopathy is characterized by an asymmetric hypertrophy of the left ventricle, especially in the interventricular septum. An outflow gradient in the left ventricle is present in twenty-five percent of cases. The disease is usually hereditary and genes responsible for the disease encode for the sarcomere proteins. The natural course is generally favourable but sometimes complications may occur, such as sudden death or congestive heart failure. Treatment remains difficult. If symptoms are not controlled by beta-blockers or verapamil, and if a pressure gradient is present, surgery with myotomy-myectomy may be proposed. Other treatments in such case are dual-chamber pacing or non-surgical septum reduction (alcohol injection). In patients with high-risk of sudden death, amiodarone or implantable cardioverter-defibrillator can be proposed.

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