Pang Kunjing, Wang Jingjin, Zhang Tingting, Wu Jinlin, Gao Yiming, Liang Yu, Ma Kai, Mao Fengqun, Pan Xiangbin, Hu Shengshou, Li Shoujun
Department of Echocardiography, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Department of Cardiac Surgery, Guangdong Academy of Medical Sciences, Guangdong Provincial People's Hospital, Guangzhou, China.
Front Cardiovasc Med. 2021 Jul 27;8:695536. doi: 10.3389/fcvm.2021.695536. eCollection 2021.
This study aimed to investigate the pathology, classification, diagnosis, and surgical prognosis of UCMV. Consecutive paediatric patients with ≥ moderate-severe mitral regurgitation (MR) and mitral stenosis (MS) were recruited between October 2016 and July 2020. UCMV was diagnosed and classified into three grades according to the involvement of chorda groups and MS presence or absence; other mitral lesions were included as controls. Of 207 eligible patients, 75 with UCMV (10.0 m [interquartile range (IQR): 6.0-21.5]) and 110 with other mitral lesions (16.0 m [IQR: 5.0-43.5]) were diagnosed using echocardiography and surgical exploration. The associated chorda groups of UCMV were confirmed to show high agreement between echocardiography and surgery (kappa = 0.857, < 0.001). At baseline surgery assessment, the UCMV group exhibited worse New York Heart Association functional class, more severe MR and MS grades, and fewer associated complex anomalies (all, < 0.05) than the control group. After a mean follow-up of 8.3 (IQR:2.7-14.4) months and adjustment for covariates, the UCMV group required longer cardiopulmonary bypass and aortic clamp times, but there were no differences in the incidence of adverse events ( = 0.584). Class III was associated with higher risk of adverse events than classes I and II ( = 0.002). The UCMV spectrum constitutes a primary pathogenesis of paediatric MV dysfunction, which can be optimally diagnosed using echocardiography. Classification based on mitral anatomy and dysfunction can predict the risk of postoperative adverse events.
本研究旨在探讨先天性二尖瓣卷曲症(UCMV)的病理学、分类、诊断及手术预后。在2016年10月至2020年7月期间,连续纳入了患有≥中重度二尖瓣反流(MR)和二尖瓣狭窄(MS)的儿科患者。UCMV根据腱索组的受累情况及MS的有无被诊断并分为三个等级;其他二尖瓣病变作为对照。在207例符合条件的患者中,75例患有UCMV(年龄10.0岁[四分位间距(IQR):6.0 - 21.5]),110例患有其他二尖瓣病变(年龄16.0岁[IQR:5.0 - 43.5]),通过超声心动图和手术探查进行诊断。UCMV的相关腱索组在超声心动图和手术之间显示出高度一致性(kappa = 0.857,P < 0.001)。在基线手术评估时,UCMV组的纽约心脏协会功能分级更差,MR和MS分级更严重,且相关复杂畸形更少(均P < 0.05),比对照组差。在平均随访8.3(IQR:2.7 - 14.4)个月并对协变量进行调整后,UCMV组需要更长的体外循环和主动脉阻断时间,但不良事件发生率无差异(P = 0.584)。Ⅲ级比Ⅰ级和Ⅱ级发生不良事件的风险更高(P = 0.002)。UCMV谱系构成小儿二尖瓣功能障碍的主要发病机制,可通过超声心动图进行最佳诊断。基于二尖瓣解剖结构和功能障碍的分类可预测术后不良事件的风险。