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胎儿右心室流出道梗阻性疾病的胎儿肺动脉瓣成形术:中国前五例的经验和结果。

Fetal Pulmonary Valvuloplasty in Fetuses with Right Ventricular Outflow Tract Obstructive Disease: Experience and Outcome of the First Five Cases in China.

机构信息

Department of Maternal-Fetal Cardiology, Guangdong Cardiovascular Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangdong Province Key Laboratory of Structural Heart Disease, Guangzhou, 510080, Guangdong, China.

Department of Pediatric Cardiology, Guangdong Cardiovascular Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangdong Province Key Laboratory of Structural Heart Disease, Guangzhou, 510080, Guangdong, China.

出版信息

Pediatr Cardiol. 2021 Feb;42(2):340-348. doi: 10.1007/s00246-020-02488-8. Epub 2020 Oct 22.

Abstract

The current study was to report our initial experiences of fetal pulmonary valvuloplasty (FPV) for fetuses with pulmonary atresia with intact ventricular septum (PA/IVS) and critical pulmonary stenosis (CPS), including case selection, technical feasibility, and the effects of FPV on utero and postnatal outcome. Two fetuses with PA/IVS and three fetuses with CPS were enrolled between September 2016 and April 2018. All fetuses were with concomitant severe right ventricular dysplasia and growth arrest. Parameters of right cardiac development and hemodynamics, including tricuspid/mitral annulus ratio (TV/MV), right ventricle/left ventricle long-axis ratio (RV/LV), tricuspid valve inflow duration/cardiac cycle ratio (TVI/CC), degree of tricuspid regurgitation (TR), and blood flow direction of arterial duct and ductus venosus, were evaluated using echocardiogram. FPV was performed trans-abdominally under ultrasound guidance. Echocardiogram was performed post-FPV and every 2-4 weeks thereafter until delivery. The median gestational age at the time of FPV was 28 weeks. From technical perspective, pulmonary balloon valvuloplasty was successfully performed and the opening of pulmonary valve was improved in all fetuses in 2-4 weeks. However, progressive restenosis was observed in four fetuses with gestation advancing, and re-atresia occurred in two PA/IVS fetuses at 36th and 37th weeks' gestation, respectively. The growth trajectories of TV/MV, RV/LV, and TVI/CC were improved in the 1st week after FPV and then slowed down along with pulmonary valve restenosis. All fetuses were born alive and underwent postnatal interventions, including pulmonary balloon valvuloplasty in three fetuses and surgical procedures in two fetuses. During follow-up, three fetuses turned to be biventricular, one became one and a half ventricular at 1-year old, and one died of neonatal infection. Although pulmonary valve restenosis might occur as gestation advancing, FPV seems to be a safe and feasible procedure to improve the growth trajectories of right heart for fetuses with PA/IVS and CPS.

摘要

本研究旨在报告我们在伴有完整室间隔的肺动脉闭锁(PA/IVS)伴严重肺动脉瓣狭窄(CPS)胎儿中进行胎儿肺动脉瓣成形术(FPV)的初步经验,包括病例选择、技术可行性以及 FPV 对宫内和产后结局的影响。2016 年 9 月至 2018 年 4 月期间共纳入 2 例 PA/IVS 胎儿和 3 例 CPS 胎儿。所有胎儿均伴有严重右心发育不良和生长停滞。采用超声心动图评估右心发育和血流动力学参数,包括三尖瓣/二尖瓣环比值(TV/MV)、右心室/左心室长轴比值(RV/LV)、三尖瓣口血流速度时间积分/心动周期比值(TVI/CC)、三尖瓣反流程度(TR)以及动脉导管和静脉导管血流方向。FPV 在超声引导下经腹进行。FPV 后以及此后每 2-4 周进行一次超声心动图检查,直至分娩。FPV 时的中位胎龄为 28 周。从技术角度来看,所有胎儿的肺动脉瓣球囊成形术均成功实施,且在 2-4 周内均改善了肺动脉瓣的开放。然而,随着胎龄的增加,4 例胎儿出现进行性再狭窄,2 例 PA/IVS 胎儿分别于 36 周和 37 周时出现再闭锁。FPV 后第 1 周,TV/MV、RV/LV 和 TVI/CC 的生长轨迹得到改善,随后随着肺动脉瓣再狭窄而减缓。所有胎儿均存活分娩,并接受了包括 3 例胎儿的肺动脉瓣球囊扩张术和 2 例胎儿的手术治疗。随访期间,3 例胎儿转为双心室,1 例 1 岁半时转为单心室,1 例因新生儿感染死亡。尽管随着胎龄的增加可能会出现肺动脉瓣再狭窄,但 FPV 似乎是一种安全可行的方法,可以改善 PA/IVS 和 CPS 胎儿右心的生长轨迹。

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