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首页> 外文期刊>Birth defects research, Part A. Clinical and molecular teratology >Exploring the potential to use data linkage for investigating the relationship between birth defects and prenatal alcohol exposure
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Exploring the potential to use data linkage for investigating the relationship between birth defects and prenatal alcohol exposure

机译:探索使用数据链接调查出生缺陷与产前酒精暴露之间关系的潜力

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摘要

This study explores the potential of data linkage to investigate the proportion of birth defects classified as alcohol-related (ARBD) by the Institutes of Medicine (IOM) that are attributable to maternal alcohol-use disorder. METHODS: Maternal alcohol-use disorder was identified using International Classification of Diseases (9th and 10th revision) codes for alcohol-related diagnoses recorded on record-linked Western Australian health, mental health, and/or drug and alcohol datasets 1983 to 2007. Children of these mothers (n=23,859) were compared with a randomly selected cohort of children born to mothers without an alcohol diagnosis, frequency-matched by maternal age, Aboriginal status, and child's birth year (n=61,370). Birth defects were identified through linkage with the Western Australian Register of Developmental Anomalies and defects with chromosomal causes were excluded. Associations between overall and individual IOM-designated ARBD and a maternal alcohol-related diagnosis recorded "during pregnancy" or "any" diagnosis (before/during/after pregnancy) was assessed using multivariate logistic regression to generate odds ratios and 95% confidence intervals. Population-attributable fractions were calculated for significant results using total population numbers. RESULTS: There was a significant association between maternal alcohol-related diagnoses recorded during pregnancy and ARBD (adjusted odds ratio, 3.14; 95% confidence interval, 2.49-3.96), with an attributable fraction of 0.57%. "Any" maternal alcohol diagnosis demonstrated a higher attributable fraction for ARBD (1.53%), with the highest attributable fractions for microcephaly (7.31%), ptosis (3.75%), atrial septal defect (2.86%), and conotruncal heart defects (2.01%). CONCLUSION: Research using linked, population-based administrative health data has the potential to advance knowledge of ARBD. Routine collection and recording of alcohol use during pregnancy for all pregnant women is required and would enhance this methodology. Birth Defects Research (Part A) 97:497-504, 2013.
机译:这项研究探索了数据链接的潜力,以调查由医学研究所(IOM)归类为酒精相关(ARBD)的出生缺陷的比例,这些缺陷归因于母亲酒精使用障碍。方法:使用国际疾病分类(第9版和第10版)代码对与酒精有关的诊断进行识别,记录在与记录有关的西澳大利亚州健康,心理健康和/或毒品和酒精数据集1983至2007年中。将这些母亲(n = 23,859)与随机选出的未进行酒精诊断的母亲所生孩子,母亲年龄,原住民身份和孩子的出生年数相匹配(n = 61,370)进行比较。通过与西澳大利亚州发育异常登记处的联系确定了出生缺陷,并且排除了染色体原因引起的缺陷。使用多元逻辑回归分析评估整体和个体IOM指定的ARBD与“怀孕期间”或“任何”诊断(怀孕之前/期间/之后)的孕妇酒精相关诊断之间的关联,以产生比值比和95%置信区间。使用总人口数计算了人口可归因的分数以获得显着结果。结果:孕妇在妊娠期间与酒精有关的诊断与ARBD之间存在显着相关性(校正比值比为3.14; 95%的置信区间为2.49-3.96),可归因分数为0.57%。 “任何”孕妇酒精诊断均显示ARBD的归因分数较高(1.53%),小头畸形(7.31%),上睑下垂(3.75%),房间隔缺损(2.86%)和圆锥瓣膜心脏缺损的归因分数最高(2.01 %)。结论:使用基于人群的链接行政健康数据进行的研究有可能增进对ARBD的了解。需要对所有孕妇进行例行收集并记录其在怀孕期间的酒精使用情况,这将加强这种方法。出生缺陷研究(Part A)97:497-504,2013。

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