Johnson Candice Y, Honein Margaret A, Dana Flanders W, Howards Penelope P, Oakley Godfrey P, Rasmussen Sonja A
National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Birth Defects Res A Clin Mol Teratol. 2012 Nov;94(11):857-63. doi: 10.1002/bdra.23086. Epub 2012 Oct 25.
In regions where prenatal screening for anencephaly and spina bifida is widespread, many cases of these defects are diagnosed prenatally. The purpose of this study was to estimate the frequency of termination of pregnancy (TOP) following prenatal diagnosis of anencephaly or spina bifida and to investigate factors associated with TOP that might lead to selection bias in epidemiologic studies.
We included articles indexed in Medline or Embase between 1990 and May 2012 reporting the frequency of TOP following prenatal diagnosis of anencephaly or spina bifida with English-language abstracts, 20 or more prenatally diagnosed cases, and at least half of the study years in 1990 or later. We summarized the frequency of TOP across studies using random-effects metaanalysis and stratified results by fetal and study characteristics.
Among the 17 studies identified, 9 included anencephaly and 15 included spina bifida. Nine were from Europe, six were from North America, and one each was from South America and Asia. The overall frequency of TOP following prenatal diagnosis was 83% for anencephaly (range, 59-100%) and 63% for spina bifida (range, 31-97%). There were insufficient data to stratify the results for anencephaly; TOP for spina bifida was more common when the prenatal diagnosis occurred at less than 24 weeks' gestation, with defects of greater severity, and in Europe versus North America.
Because underascertainment of birth defects might be more likely when the pregnancy ends in TOP and TOP is associated with fetal characteristics, selection bias is possible in epidemiologic studies of anencephaly or spina bifida.
在无脑儿和脊柱裂产前筛查普及的地区,许多此类缺陷病例在产前被诊断出来。本研究的目的是估计产前诊断为无脑儿或脊柱裂后终止妊娠(TOP)的频率,并调查与TOP相关的因素,这些因素可能导致流行病学研究中的选择偏倚。
我们纳入了1990年至2012年5月期间在Medline或Embase中索引的文章,这些文章报告了产前诊断为无脑儿或脊柱裂后TOP的频率,有英文摘要,20例或更多产前诊断病例,且至少一半研究年份在1990年或之后。我们使用随机效应荟萃分析总结了各项研究中TOP的频率,并按胎儿和研究特征对结果进行分层。
在纳入的17项研究中,9项包括无脑儿,15项包括脊柱裂。9项来自欧洲,6项来自北美,1项来自南美,1项来自亚洲。产前诊断后TOP的总体频率,无脑儿为83%(范围59 - 100%),脊柱裂为63%(范围31 - 97%)。无脑儿结果分层的数据不足;脊柱裂的TOP在妊娠小于24周时产前诊断、缺陷严重程度更高以及在欧洲比北美更常见。
由于当妊娠以TOP结束时出生缺陷可能更易漏报,且TOP与胎儿特征相关,在无脑儿或脊柱裂的流行病学研究中可能存在选择偏倚。