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1990 - 1991年神经管缺陷出生相关的既往情况。国家遗传疾病咨询保密调查指导委员会。

Antecedent circumstances surrounding neural tube defect births in 1990-1991. The Steering Committee of the National Confidential Enquiry into Counselling for Genetic Disorders.

作者信息

Williamson P, Alberman E, Rodeck C, Fiddler M, Church S, Harris R

机构信息

Genetic Enquiry Centre, St Mary's Hospital, Manchester, UK.

出版信息

Br J Obstet Gynaecol. 1997 Jan;104(1):51-6. doi: 10.1111/j.1471-0528.1997.tb10649.x.

Abstract

OBJECTIVE

To investigate births with neural tube defects at a time when most districts were screening for the condition. The objective was to document the circumstances surrounding each affected birth and assess the care provided against given standards.

DESIGN

Retrospective review of antenatal casenotes by the obstetric team.

POPULATION

Three hundred and eight births in England and Wales in 1990 to 1991 were reported to the Office of Population Census Survey (OPCS) to involve neural tube defects. Sufficient information was available to identify both the woman and the obstetrician in 213 pregnancies. Details were obtained from a questionnaire completed by the obstetric team for 168 (79%). In 20/168 cases either the reported outcome was not a live birth/stillbirth or the pregnancy did not involve a neural tube defect: eight resulted in a 'normal' infant, eight were terminated and in four the abnormality was not a neural tube defect. Thus 148 eligible cases were available for analysis.

RESULTS

Of the 148 births, the anomaly was not detected prenatally or detected later than 25 weeks of gestation in 98 cases (66%), diagnosed in a multiple pregnancy in 24 (16%) and diagnosed prenatally but the woman chose to continue the pregnancy in 26 (18%). Of the 98 births not detected prenatally or detected late during pregnancy, the surrounding circumstances were that screening was declined in six cases (4%), screening was not offered due to late booking in 30 (20%), serum alpha-fetoprotein screening gave a false negative result in eight (5%), ultrasound screening gave a false negative result in 29 (20%), both screening methods gave false negative results in 17 (11%) and other reasons in eight (5%). The estimated sensitivity of ultrasound screening for anencephaly was 100%. For spina bifida the estimated sensitivity for singleton pregnancies is higher for serum alpha-fetoprotein screening, 84% to 92%, than ultrasound screening, 70% to 84%, for a range of assumptions regarding the degree of under-reporting to OPCS of live births and terminations.

CONCLUSIONS

Late booking precluded the offer of screening tests in a substantial proportion (22%) of cases. The presence of multiple fetuses including one or more with a neural tube defect was a serious additional complication in prenatal screening, diagnosis and counselling. Screening for neural tube defects was widespread in 1990 to 1991, although variations in the services provided were documented. Ultrasound scanning was a major component but was associated with a lower sensitivity than maternal serum alpha-fetoprotein screening for neural tube defects other than anencephaly.

摘要

目的

在大多数地区对神经管缺陷进行筛查之际,调查神经管缺陷患儿的出生情况。目的是记录每例受影响分娩的相关情况,并对照既定标准评估所提供的护理。

设计

产科团队对产前病历进行回顾性审查。

研究对象

1990年至1991年在英格兰和威尔士,向人口普查调查办公室(OPCS)报告的308例涉及神经管缺陷的分娩。在213例妊娠中,有足够信息可识别产妇和产科医生。详细信息来自产科团队填写的168份(79%)问卷。在168例病例中,有20例报告的结局不是活产/死产,或者妊娠不涉及神经管缺陷:8例分娩出“正常”婴儿,8例终止妊娠,4例异常情况并非神经管缺陷。因此,有148例符合条件的病例可供分析。

结果

在148例分娩中,98例(66%)在产前未检测到异常或在妊娠25周后才检测到,24例(16%)在多胎妊娠中被诊断出,26例(18%)在产前被诊断出但产妇选择继续妊娠。在98例产前未检测到或在孕期晚期才检测到的分娩中,相关情况如下:6例(4%)拒绝筛查,30例(20%)因登记过晚未提供筛查,8例(5%)血清甲胎蛋白筛查结果为假阴性,29例(20%)超声筛查结果为假阴性,17例(11%)两种筛查方法结果均为假阴性,8例(5%)为其他原因。超声筛查无脑儿的估计敏感度为100%。对于脊柱裂,就向OPCS漏报活产和终止妊娠的程度的一系列假设而言,血清甲胎蛋白筛查对单胎妊娠的估计敏感度较高,为84%至92%,高于超声筛查的70%至84%。

结论

登记过晚导致相当比例(22%)的病例无法进行筛查。多胎妊娠(包括一个或多个患有神经管缺陷的胎儿)的存在是产前筛查、诊断和咨询中的一个严重额外并发症。1990年至1991年期间,神经管缺陷筛查较为普遍,尽管记录了所提供服务的差异。超声扫描是主要组成部分,但对于除无脑儿之外的神经管缺陷,其敏感度低于母体血清甲胎蛋白筛查。

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