Suppr超能文献

通过产妇访谈获取的出生缺陷病史评估。

Evaluation of birth defect histories obtained through maternal interviews.

作者信息

Rasmussen S A, Mulinare J, Khoury M J, Maloney E K

机构信息

University of Florida College of Medicine, Gainesville.

出版信息

Am J Hum Genet. 1990 Mar;46(3):478-85.

Abstract

Etiologic studies of birth defects often use family history information provided by parents of patients. The validity of this information has not been adequately assessed. Using data from the Atlanta Birth Defects Case-Control study, we evaluated sensitivity, specificity, and positive predictive value of mothers' responses regarding the presence of birth defects in their offspring. A total of 4929 mothers of infants with major structural defects ascertained by the Metropolitan Atlanta Congenital Defects Program and a total of 3,029 mothers of normal infants were asked whether their babies had had a birth defect or a health problem diagnosed during the first year of life. Interviewers and coders of maternal responses were blinded to the case-control status of infants. Sensitivity (the proportion of case mothers who gave responses that could be coded as denoting a major birth defect) was 61%. Specificity (the proportion of control mothers who gave responses that could not be coded as denoting a major birth defect) was 98%. The positive predictive value (the proportion of mothers who gave a major-birth-defect response who in fact had babies with major birth defects) was estimated as 47%. Sensitivity, specificity, and positive predictive value varied by maternal sociodemographic factors such as race and education, as well as by type of defect. These results suggest that family history data obtained through maternal interviews should be cautiously interpreted and, if not properly validated, may alter estimates of recurrence risks.

摘要

出生缺陷的病因学研究通常使用患者父母提供的家族史信息。但这一信息的有效性尚未得到充分评估。利用亚特兰大出生缺陷病例对照研究的数据,我们评估了母亲对于其后代是否存在出生缺陷的回答的敏感性、特异性和阳性预测值。由大亚特兰大先天性缺陷项目确诊的4929名患有主要结构缺陷婴儿的母亲,以及3029名正常婴儿的母亲被问及她们的宝宝在出生后第一年是否被诊断出有出生缺陷或健康问题。母亲回答的访谈者和编码人员对婴儿的病例对照状态不知情。敏感性(病例组母亲中给出的回答可被编码为表示存在主要出生缺陷的比例)为61%。特异性(对照组母亲中给出的回答不能被编码为表示存在主要出生缺陷的比例)为98%。阳性预测值(给出主要出生缺陷回答的母亲中,其婴儿实际患有主要出生缺陷的比例)估计为47%。敏感性、特异性和阳性预测值因母亲的社会人口学因素(如种族和教育程度)以及缺陷类型而异。这些结果表明,通过母亲访谈获得的家族史数据应谨慎解读,若未得到适当验证,可能会改变复发风险的估计。

相似文献

8
The National Birth Defects Prevention Study.国家出生缺陷预防研究
Public Health Rep. 2001;116 Suppl 1(Suppl 1):32-40. doi: 10.1093/phr/116.S1.32.

引用本文的文献

本文引用的文献

6
Accuracy of spontaneous abortion recall.自然流产回忆的准确性。
Am J Epidemiol. 1984 Nov;120(5):727-33. doi: 10.1093/oxfordjournals.aje.a113940.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验