Surgical Repair of Secondary Subaortic Stenosis in Congenital Heart Disease Without Initial Subaortic Obstruction.

Yuefeng Cao, Xiangming Fan
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Abstract

BACKGROUND Secondary subaortic stenosis (SSS) is a rare heart disease of the left ventricular outflow tract (LVOT). It usually occurs after cardiovascular correction with or without initial left ventricular outflow tract obstruction (LVOTO). Because most patients with SSS are asymptomatic, many do not realize the need for reoperation until the obstruction worsens. Few studies suggest the characteristics and reasons of SSS without initial SAS. We conducted a retrospective study to describe the characteristics and surgical outcomes of these patients. METHODS In this study, we examined a single-center retrospective cohort of SSS patients without initial SAS undergoing resection from 2010 to 2019. Patients are defined as secondary subaortic obstruction requiring surgery after cardiovascular correction. Demographics, perioperative findings, and clinical data were analyzed. RESULTS Twenty-three patients had undergone secondary cardiac surgery for SSS without initial SAS during 10 years in our center. The median age at operation was 7.3 (4.0-13.5) years. In this study, the most commonly associated cardiac lesions were ventricular septal defect (VSD), atrioventricular septal defect (AVSD), patent ductus arteriosus (PDA), and coarctation arch hypoplasia (COA). The surgical techniques included membranous resection of five patients, fibromuscular resection of 17 patients, and reconstruction of the intraventricular baffle of one patient. The results of surgery in these patients are satisfied. The average LVOT gradient at the last follow up was 14.9 (7.8-26.2) mmHg. There was no operative mortality. Two patients had postoperative complications. The median follow-up period was 2.9 (1.1-4.3) years with one late death. Two patients (8.7%) had recurrence of stenosis. CONCLUSIONS Secondary subaortic stenosis is an uncommon heart disease. The reason is related to several causes, including missed diagnosis, unnoticed abnormalities of LVOT, and further changes of geometric morphology by intracardiac surgery. The results of surgery in these patients are satisfied. However, the recurrence of stenosis is still frequent.
无主动脉下梗阻的先天性心脏病继发性主动脉下狭窄的外科修复。
背景:继发性主动脉下狭窄(SSS)是一种罕见的左心室流出道(LVOT)心脏病。它通常发生在心血管矫正后,伴有或不伴有初始左心室流出道梗阻(LVOTO)。由于大多数SSS患者是无症状的,许多人直到梗阻恶化才意识到需要再次手术。很少有研究提出无初始SAS的SSS的特点和原因。我们进行了一项回顾性研究来描述这些患者的特征和手术结果。方法在本研究中,我们对2010年至2019年无初始SAS切除的SSS患者进行了单中心回顾性队列研究。患者被定义为继发性主动脉下梗阻,在心血管矫正后需要手术。分析人口统计学、围手术期发现和临床资料。结果本中心10年间有23例无SAS的SSS患者接受了二次心脏手术。手术年龄中位数为7.3岁(4.0 ~ 13.5岁)。在本研究中,最常见的相关心脏病变是室间隔缺损(VSD)、房室间隔缺损(AVSD)、动脉导管未闭(PDA)和缩窄弓发育不全(COA)。手术技术包括5例膜性切除,17例纤维性肌肉切除,1例脑室内挡板重建。这些患者的手术效果令人满意。最后一次随访时平均LVOT梯度为14.9 (7.8-26.2)mmHg。无手术死亡率。2例患者出现术后并发症。中位随访期为2.9(1.1-4.3)年,1例晚期死亡。2例(8.7%)狭窄复发。结论继发性主动脉下狭窄是一种少见的心脏病。其原因与漏诊、未注意到的LVOT异常、心内手术进一步改变几何形态等因素有关。这些患者的手术效果令人满意。然而,狭窄的复发仍然是频繁的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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