Department of OB&GYN, Justus-Liebig-University and UKGM, Division of Prenatal Medicine, Giessen, Germany.
Köln, preanatalplus.de, Köln, Germany.
Ultraschall Med. 2020 Oct;41(5):504-513. doi: 10.1055/a-0753-0008. Epub 2018 Nov 19.
The aim of our retrospective evaluation was to compare the outcome of patients with prenatal and postnatal diagnosis of Tetralogy of Fallot (TOF) and to analyze prenatal echocardiographic parameters predicting intervention within 30 days postnatal.
We evaluated 142 patients in our pediatric heart center and prenatal diagnosis center and prenatal practice Praenatal plus in Cologne between 01/08-06/16.
Within the prenatal diagnosis group, 6/74 fetuses (8.1 %) had TOF with pulmonary atresia (TOF-PA), and 6 (8.1 %) had absent pulmonary valve syndrome (TOF-APVS). 14 (18.9 %) had an abnormal karyotype including 9/14 (64.3 %) with microdeletion 22q11.2. 25 (33.8 %) had extracardiac malformation. 4 (5.4 %) had agenesis of ductus arteriosus (DA), 22 (29.7 %) had right aortic arch (RAA) and 9 (12.2 %) had major aortopulmonary collateral arteries (MAPCAs). Within the postnatal diagnosis group, no patient had TOF-PA, 4/68 (5.9 %) had TOF-APVS. 12 (17.6 %) had extracardiac malformations, 9 (13.2 %) had an abnormal karyotype including 2/9 with microdeletion 22q11.2. 10 (14.7 %) had RAA, 9 (13.2 %) had MAPCAs. There were no cases with agenesis of DA. Increasing z-score values of the left/right pulmonary artery (LPA/RPA) prenatally were associated with a lower probability for early postnatal intervention (RPA: p = 0.017; LPA: p = 0.013). Within the prenatal diagnosis group, 12 of 41 (29.3 %) live-born patients with follow-up and intention to treat needed early intervention versus 7 (10.3 %) in the postnatal diagnosis group (p = 0.02). Within the postnatal diagnosis group, there were no deaths, while 2 (4.9 %) post-intervention deaths occurred in the prenatal diagnosis group.
There are no significant differences concerning post-intervention survival in the prenatal diagnosis group versus the postnatal diagnosis group. Complex cases may be underrepresented in the postnatal diagnosis group. Smaller RPA/LPA values prenatally seem to be associated with early postnatal intervention.
本回顾性研究旨在比较产前和产后诊断法洛四联症(TOF)患者的结局,并分析预测产后 30 天内干预的产前超声心动图参数。
我们评估了 2016 年 6 月 1 日至 2016 年 6 月 16 日期间在我们的儿科心脏中心、产前诊断中心和科隆的产前Praenatal plus 中心的 142 名患者。
在产前诊断组中,74 例胎儿中有 6 例(8.1%)存在肺动脉闭锁(TOF-PA),6 例(8.1%)存在肺动脉瓣缺如综合征(TOF-APVS)。14 例(18.9%)存在异常核型,包括 9 例(64.3%)存在 22q11.2 微缺失。25 例(33.8%)存在心脏外畸形。4 例(5.4%)存在动脉导管未闭(DA)发育不全,22 例(29.7%)存在右主动脉弓(RAA),9 例(12.2%)存在主肺动脉侧支动脉(MAPCAs)。在产后诊断组中,无 TOF-PA 患者,68 例中有 4 例(5.9%)存在 TOF-APVS。12 例(17.6%)存在心脏外畸形,9 例(13.2%)存在异常核型,包括 2 例(22q11.2 微缺失)。10 例(14.7%)存在 RAA,9 例(13.2%)存在 MAPCAs。无 DA 发育不全。产前左/右肺动脉(LPA/RPA)Z 评分值增加与早期产后干预的可能性降低相关(RPA:p=0.017;LPA:p=0.013)。在产前诊断组中,有 41 例(29.3%)活产并随访且有早期干预意向的患者需要早期干预,而产后诊断组中只有 7 例(10.3%)(p=0.02)。产后诊断组中无死亡,而产前诊断组中有 2 例(4.9%)干预后死亡。
产前诊断组与产后诊断组的术后生存无显著差异。产后诊断组可能存在复杂病例代表性不足的情况。产前 RPA/LPA 值较小似乎与早期产后干预相关。