Department of Pharmaceutical Outcomes and Policy, College of Pharmacy, University of Florida, Gainesville, Florida, USA.
Office of Surveillance and Epidemiology, Center for Drug Evaluation and Research, United States Food and Drug Administration, Silver Spring, Maryland, USA.
Pharmacoepidemiol Drug Saf. 2020 Nov;29(11):1414-1422. doi: 10.1002/pds.5126. Epub 2020 Sep 9.
Accurate ascertainment of gestational age (GA) has been a challenge in perinatal epidemiologic research. To date, no study has validated GA algorithms in Medicaid Analytic eXtract (MAX).
We linked livebirths of mothers enrolled in Medicaid ≥30 days after delivery in 1999-2010 MAX to state birth certificates. We used clinical/obstetric estimate of gestation on the birth certificates as gold standard to validate claims-based GA algorithms. We calculated the proportions of deliveries with algorithm-estimated GA within 1-/2-weeks of the gold standard, the sensitivity, specificity, and positive/negative predictive value (PPV/NPV) of exposure to select medications during specific gestation windows, and quantified the impact of exposure misclassification on hypothetical relative risk (RR) estimates.
We linked 1 336 495 eligible deliveries. Within 1-week agreement was 77%-80% overall and 47%-56% for preterm deliveries. The trimester-specific drug exposure status had high sensitivities and PPVs (88.5%-98.5%), and specificities and NPVs (>99.0%). Assuming a hypothetical RR of 2.0, bias associated with exposure misclassification during first trimester ranged from 10% to 40% under non-differential/differential misclassification assumptions.
Claims-based GA algorithms had good agreement with the gold standard overall, but lower agreement among preterm deliveries, potentially resulting in biased risk estimated for pregnancy exposure evaluations.
准确确定孕龄(GA)一直是围产期流行病学研究中的一个挑战。迄今为止,还没有研究在 Medicaid Analytic eXtract(MAX)中验证 GA 算法。
我们将 1999 年至 2010 年 MAX 中分娩后至少 30 天加入 Medicaid 的母亲的活产与州出生证明相联系。我们使用出生证明上的临床/产科估计胎龄作为金标准来验证基于索赔的 GA 算法。我们计算了算法估计的 GA 与金标准相差 1/2 周的分娩比例、在特定胎龄窗口暴露于特定药物的敏感性、特异性和阳性/阴性预测值(PPV/NPV),并量化了暴露错误分类对假设相对风险(RR)估计的影响。
我们将 1 336 495 例合格分娩联系起来。总体上,1 周内的一致性为 77%-80%,而早产的一致性为 47%-56%。特定妊娠阶段的药物暴露状态具有较高的敏感性和阳性预测值(88.5%-98.5%),特异性和阴性预测值(>99.0%)。假设 RR 为 2.0,在非差异/差异错误分类假设下,与第一孕期暴露错误分类相关的偏倚范围为 10%-40%。
基于索赔的 GA 算法总体上与金标准具有良好的一致性,但在早产分娩中一致性较低,这可能导致对妊娠暴露评估的风险估计存在偏差。