Sathanandam Shyam K, Philip Ranjit, Gamboa David, Van Bergen Andrew, Ilbawi Michel N, Knott-Craig Christopher, Waller B Rush, Javois Alexander J, Cuneo Bettina F
1Advocate Children's Hospital,Oak Lawn,Illinois,United States of America.
2University of Tennessee Health Science Center,LeBonheur Children's Hospital Memphis,Tennessee,United States of America.
Cardiol Young. 2016 Aug;26(6):1072-81. doi: 10.1017/S1047951115001791. Epub 2015 Sep 8.
Introduction Hypoplastic left heart syndrome with an intact atrial septum is a poor predictor of outcomes. Prenatal assessment of pulmonary venous Doppler and emergent postnatal cardiac intervention may be associated with better outcomes. Materials and methods A retrospective review of all hypoplastic left heart syndrome patients in two centres over a 5-year period was performed. Group 1 included patients with adequate inter-atrial communication. Group 2 included patients with prenatal diagnosis with an intact atrial septum who had immediate transcatheter intervention. Group 3 included patients with intact atrial septum who were not prenatally diagnosed and underwent either delayed intervention or no intervention before stage 1 palliation. Primary outcome was survival up to stage 2 palliation.
The incidence of hypoplastic left heart syndrome with a restrictive atrial communication was 11.2% (n=19 of 170). Overall survival to stage 2 or heart transplantation was 85% and 67% for Groups 1 and 2, respectively (n=129/151, n=8/12; p=0.03), and 0% (n=0/7) for Group 3. Survival benefits were observed between Groups 2 and 3 (p<0.001). Foetal pulmonary vein Doppler reverse/forward velocity time integral ratio of ⩾18% (sensitivity, 0.99, 95% CI, 0.58-1; specificity, 0.99, 95% CI, 0.96-1) was predictive of the need for emergent left atrial decompression.
Using a multidisciplinary approach and foetal pulmonary vein Doppler, time-saving measures can be instituted by delivering prenatally diagnosed neonates with hypoplastic left heart syndrome with intact atrial septum close to the cardiac catheterisation suite where left atrial decompression can be performed quickly and safely that may improve survival.
引言 房间隔完整的左心发育不全综合征预后较差。产前肺静脉多普勒评估和出生后紧急心脏干预可能与更好的预后相关。材料与方法 对两个中心5年内所有左心发育不全综合征患者进行回顾性研究。第1组包括房间隔交通适当的患者。第2组包括产前诊断为房间隔完整且立即接受经导管干预的患者。第3组包括房间隔完整但未产前诊断且在1期姑息治疗前接受延迟干预或未接受干预的患者。主要结局是存活至2期姑息治疗。
房间隔限制性交通的左心发育不全综合征发生率为11.2%(170例中的19例)。第1组和第2组分别有85%和67%的患者存活至2期或接受心脏移植(n = 129/151,n = 8/12;p = 0.03),第3组为0%(n = 0/7)。第2组和第3组之间观察到生存获益(p < 0.001)。胎儿肺静脉多普勒反向/正向速度时间积分比≥18%(敏感性,0.99,95%可信区间,0.58 - 1;特异性,0.99,95%可信区间,0.96 - 1)可预测紧急左心房减压的必要性。
采用多学科方法和胎儿肺静脉多普勒,对于产前诊断为房间隔完整的左心发育不全综合征新生儿,可在靠近心脏导管室的地方分娩,以便能快速安全地进行左心房减压,从而采取节省时间的措施,这可能提高生存率。