Department of Epidemiology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Prenat Diagn. 2017 Nov;37(11):1100-1111. doi: 10.1002/pd.5148. Epub 2017 Oct 6.
To provide prognostic information to help parents to reach an informed decision about termination or continuation of the pregnancy and to shape peripartum policy based on a large European cohort.
Thirteen registries from the European Surveillance of Congenital Anomalies (EUROCAT) network contributed data from January 1, 1998, to December 31, 2011. Terminations for fetal anomalies were excluded. Chromosomal anomalies, syndromes and isolated anomaly groups were distinguished according to EUROCAT guidelines. Perinatal mortality, stillbirths, and early and late neonatal mortality rates (NMRs) were analyzed by anomaly group and gestational age.
Among 73 337 cases, perinatal mortality associated with congenital anomaly was 1.27 per 1000 births (95% confidence interval, 1.23-1.31). Average stillbirth rate was 2.68% (range 0%-51.2%). Early and late NMR were 2.75% (range 0%-46.7%) and 0.97% (range 0%-17.9%), respectively. Chromosomal anomalies and syndromes, and most isolated anomalies, had significant differences regarding timing of fetal demise compared to the general population. Chromosomal and central nervous system anomalies had higher term stillbirth rates.
We found relevant differences between anomalies regarding rates of stillbirth, NMR, and timing by gestational age. Our data can help parents to decide about their unborn child with a congenital anomaly and help inform maternal-fetal medicine specialists regarding peripartum management.
提供预后信息,帮助父母在知情的情况下决定终止或继续妊娠,并根据大型欧洲队列制定围产期政策。
欧洲先天性畸形监测(EUROCAT)网络的 13 个登记处提供了 1998 年 1 月 1 日至 2011 年 12 月 31 日的数据。排除了因胎儿畸形而终止妊娠的病例。根据 EUROCAT 指南,将染色体异常、综合征和孤立性异常组区分开来。根据异常组和胎龄分析围产儿死亡率、死产和早、晚期新生儿死亡率(NMR)。
在 73337 例病例中,先天性畸形相关的围产儿死亡率为每 1000 例活产 1.27 例(95%置信区间,1.23-1.31)。平均死产率为 2.68%(范围 0%-51.2%)。早、晚期 NMR 分别为 2.75%(范围 0%-46.7%)和 0.97%(范围 0%-17.9%)。与一般人群相比,染色体异常和综合征以及大多数孤立性异常在胎儿死亡时间上有显著差异。染色体和中枢神经系统异常的足月死产率较高。
我们发现,在死产率、NMR 和胎龄方面,不同异常之间存在显著差异。我们的数据可以帮助父母决定他们未出生的患有先天性畸形的孩子,并为围产期管理提供信息。