Mitral valve repair during septal myectomy in obstructive hypertrophic cardiomyopathy

Q4 Medicine
S. Budagaev, Maksat Zhakayev, R. Tuleutayev, Michel Vorontsov, Artem Nikitenko, Zh. N. Nurbay, Daniyar Kunapyanov, M. Pashimov
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引用次数: 0

Abstract

Hypertrophic cardiomyopathy is a common genetic heart disease characterized predominantly by non-dilated hypertrophy of the left ventricle, in the absence of other cardiac, systemic, or metabolic diseases that can cause the observed degree of hypertrophy. The main features of left ventricular outflow tract obstruction include anatomical - basal septal hypertrophy in combination with a relatively small left ventricular cavity, leading to a change in the geometry of the outflow tract from the left ventricle, pushing the mitral valve apparatus forward, and functional - systolic anterior motion of elongated mitral valve leaflets with subsequent mitral-septal contact. Primary anatomical changes of the mitral valve make the valve more susceptible to abnormal flow vectors generated in the left ventricle cavity, creating the conditions for systolic anterior motion and mitral regurgitation. Septal myectomy, performed by experienced surgeons in specialized centers, eliminates obstruction at all levels of the left ventricular outflow tract, with a clinical success rate of 90-95% and a mortality rate of less than 1%. Some surgeons complement septal myectomy with intervention on the mitral valve, taking into account anatomical features when isolated septal myectomy may be ineffective. The choice of the most optimal concurrent intervention on the mitral valve during septal myectomy is undefined. Techniques for valve-sparing mitral valve surgery have been developed, including resection of secondary chords, edge-to-edge repair, anterior leaflet plication, and others. This review presents the hemodynamic outcomes of concomitant interventions on the mitral valve in addition to septal myectomy in patients with obstructive hypertrophic cardiomyopathy.
梗阻性肥厚性心肌病中隔肌切除术中二尖瓣修复
肥厚性心肌病是一种常见的遗传性心脏病,其主要特征是左心室非扩张性肥厚,没有其他心脏、全身或代谢性疾病可引起所观察到的肥厚程度。左室流出道梗阻的主要特征包括解剖-基底间隔肥大合并相对较小的左室腔,导致左心室流出道的几何形状改变,推动二尖瓣装置向前移动,延长的二尖瓣小叶在随后的二尖瓣-间隔接触时发生功能性收缩前移。二尖瓣的原发性解剖改变使其更易受到左心室腔内产生的异常流矢量的影响,为收缩前运动和二尖瓣反流创造了条件。由专业中心经验丰富的外科医生实施的室间隔肌瘤切除术,可消除左心室流出道各级梗阻,临床成功率为90-95%,死亡率低于1%。一些外科医生考虑到孤立性鼻中隔切除术可能无效的解剖特点,在二尖瓣介入手术的基础上补充了鼻中隔切除术。在室间隔肌切除术中,二尖瓣的最佳并发干预选择是不明确的。保留二尖瓣手术的技术已经发展起来,包括切除第二索、边缘到边缘修复、前小叶折叠等。这篇综述介绍了阻塞性肥厚性心肌病患者在二尖瓣切除的同时进行干预的血流动力学结果。
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来源期刊
CiteScore
0.20
自引率
0.00%
发文量
45
审稿时长
5 weeks
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