Boyd P A, Wellesley D G, De Walle H E, Tenconi R, Garcia-Minaur S, Zandwijken G R, Stoll C, Clementi M
Prenatal Diagnosis Service, Women's Centre, Oxford Radcliffe Hospital, Headington, UK.
J Med Screen. 2000;7(4):169-74. doi: 10.1136/jms.7.4.169.
Evaluation of prenatal diagnosis of neural tube defects by ultrasound examination in unselected populations across Europe.
Prenatal ultrasound units in areas that report to contributing congenital malformation registers.
All cases with a suspected or confirmed neural tube defect and delivered within the 30 month study period were identified from 18 Congenital Malformation Registers from 11 European countries. Data on the pregnancy, prenatal scans, outcome of pregnancy, and information on different screening policies for each country were analysed.
670766 deliveries occurred in the area covered by the registers during the study period. A neural tube defect was diagnosed at delivery in 542 cases. In 84% of these, the lesion was isolated (166 anencephaly, 252 spina bifida, 35 encephalocele). Of the 166 isolated cases with anencephaly, 96% were correctly identified prenatally; one was missed on scan, two were wrongly diagnosed, and four were not scanned (sensitivity 98%). 84% of the prenatal diagnoses were made before 24 weeks' gestation; 86% of isolated anencephalic pregnancies were terminated. Of the 252 cases of isolated spina bifida, 171 (68%) were correctly identified prenatally; 66% of these before 24 weeks' gestation. The diagnosis was missed on scan in 60 cases and 21 were not scanned (sensitivity 75%). The mean reduction in birth prevalence because of termination of pregnancy for spina bifida was 49% (range 6-100%). There was a wide variation between centres in prenatal detection rate (33-100%), termination of pregnancy of prenatally diagnosed cases (17-100%), and gestation both at diagnosis and termination of pregnancy.
A high prenatal detection rate for anencephaly was reported by all registers. There is a large variation in prenatal detection and termination rates for spina bifida between centres, reflecting differences both in policy and culture.
评估在欧洲未经过筛选的人群中通过超声检查对神经管缺陷进行产前诊断的情况。
向先天性畸形登记处上报数据的地区的产前超声科室。
从11个欧洲国家的18个先天性畸形登记处中识别出在30个月研究期内分娩的所有疑似或确诊神经管缺陷病例。分析了妊娠、产前扫描、妊娠结局的数据以及每个国家不同筛查政策的信息。
在研究期间,登记处覆盖地区共发生670766例分娩。542例在分娩时被诊断为神经管缺陷。其中84%为单发病变(166例无脑儿、252例脊柱裂、35例脑膨出)。在166例单发无脑儿病例中,96%在产前被正确识别;1例漏诊,2例误诊,4例未进行扫描(敏感性98%)。84%的产前诊断在妊娠24周前做出;86%的单发无脑儿妊娠被终止。在252例单发脊柱裂病例中,171例(68%)在产前被正确识别;其中66%在妊娠24周前做出诊断。60例漏诊,21例未进行扫描(敏感性75%)。因脊柱裂妊娠终止导致的出生患病率平均降低49%(范围6%-100%)。各中心在产前检测率(33%-100%)、产前诊断病例的妊娠终止率(17%-100%)以及诊断和妊娠终止时的孕周方面存在很大差异。
所有登记处均报告无脑儿的产前检测率较高。各中心之间脊柱裂的产前检测率和终止率差异很大,反映出政策和文化方面的差异。