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Multiwave validation sampling for error‐prone electronic health records

Author

Listed:
  • Bryan E. Shepherd
  • Kyunghee Han
  • Tong Chen
  • Aihua Bian
  • Shannon Pugh
  • Stephany N. Duda
  • Thomas Lumley
  • William J. Heerman
  • Pamela A. Shaw

Abstract

Electronic health record (EHR) data are increasingly used for biomedical research, but these data have recognized data quality challenges. Data validation is necessary to use EHR data with confidence, but limited resources typically make complete data validation impossible. Using EHR data, we illustrate prospective, multiwave, two‐phase validation sampling to estimate the association between maternal weight gain during pregnancy and the risks of her child developing obesity or asthma. The optimal validation sampling design depends on the unknown efficient influence functions of regression coefficients of interest. In the first wave of our multiwave validation design, we estimate the influence function using the unvalidated (phase 1) data to determine our validation sample; then in subsequent waves, we re‐estimate the influence function using validated (phase 2) data and update our sampling. For efficiency, estimation combines obesity and asthma sampling frames while calibrating sampling weights using generalized raking. We validated 996 of 10,335 mother‐child EHR dyads in six sampling waves. Estimated associations between childhood obesity/asthma and maternal weight gain, as well as other covariates, are compared to naïve estimates that only use unvalidated data. In some cases, estimates markedly differ, underscoring the importance of efficient validation sampling to obtain accurate estimates incorporating validated data.

Suggested Citation

  • Bryan E. Shepherd & Kyunghee Han & Tong Chen & Aihua Bian & Shannon Pugh & Stephany N. Duda & Thomas Lumley & William J. Heerman & Pamela A. Shaw, 2023. "Multiwave validation sampling for error‐prone electronic health records," Biometrics, The International Biometric Society, vol. 79(3), pages 2649-2663, September.
    • Handle: RePEc:bla:biomet:v:79:y:2023:i:3:p:2649-2663
    DOI: 10.1111/biom.13713
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    References listed on IDEAS

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