Durand I, Deverriere G, Thill C, Lety A S, Parrod C, David N, Barre E, Hazelzet T
Department of Pediatrics, Rouen University Hospital, 1 Rue de Germont, 76031, Rouen Cedex, France,
Pediatr Cardiol. 2015 Aug;36(6):1248-54. doi: 10.1007/s00246-015-1153-1. Epub 2015 Apr 7.
The objective of this study was to assess the ability of different parameters to identify fetuses requiring neonatal care for coarctation of the aorta (CoA). Between January 2003 and December 2012, 175 fetuses referred for great vessel disproportion were divided into two groups: group A (n = 51) with high risk of CoA and delivery planned in tertiary care referral center and group B (n = 124) with no increased risk of CoA. In group A, diagnosis of CoA was confirmed in 38/51 (74 %). In group B, 2/124 had CoA. Multiple logistic regression analysis identified the best combination as diffusely hypoplastic and/or angular aortic arches, ventricular septal defect and aortic valve diameter <5 mm at 36-week gestational age (GA). Positive predictive value was 75 % when vessel disproportion was noted before 28-week GA and 73 % in the third trimester. Postnatal diagnosis involved 38 cases of CoA which had not been referred. One case of CoA diagnosed after birth was referred prenatally for difficulty of screening without any defect. The results of our prospective study are in agreement with those of previous series, but our false positive rate was lower especially when the diagnosis of vascular disproportion was made at third trimester. The performance of fetal cardiac screening does not seem to be very good, but prenatal diagnosis is probably not always possible: Among our three false negative cases, two had isolated vascular disproportion and the third no risk factors.
本研究的目的是评估不同参数识别因主动脉缩窄(CoA)需要新生儿护理的胎儿的能力。在2003年1月至2012年12月期间,175例因大血管比例失调转诊的胎儿被分为两组:A组(n = 51),CoA风险高且计划在三级医疗转诊中心分娩;B组(n = 124),CoA风险未增加。在A组中,51例中有38例(74%)CoA诊断得到证实。在B组中,124例中有2例患有CoA。多因素逻辑回归分析确定最佳组合为弥漫性发育不全和/或角状主动脉弓、室间隔缺损以及孕36周时主动脉瓣直径<5 mm。孕28周前发现血管比例失调时阳性预测值为75%,孕晚期为73%。产后诊断涉及38例未转诊的CoA病例。1例出生后诊断为CoA的病例因筛查困难且无任何缺陷而在产前被转诊。我们前瞻性研究的结果与之前系列研究的结果一致,但我们的假阳性率较低,尤其是在孕晚期做出血管比例失调诊断时。胎儿心脏筛查的表现似乎不太理想,但产前诊断可能并非总是可行:在我们的三例假阴性病例中,两例有孤立的血管比例失调,第三例无危险因素。