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Stephany N. Duda

Publications and source records attributed to Stephany N. Duda.

3 recordsLinked to original sources

Authentic Multinational Federated Time-to-Event Analyses Among People with HIV in Latin America

Multinational HIV cohort studies face regulatory barriers to cross-border sharing of individual participant data, limiting centralized pooled analyses. Federated statistical methods, which exchange only aggregated information, offer a privacy-preserving alternative but have rarely been examined in real-world distributed environments for HIV research. Here, we evaluate the feasibility and analytical performance of a communication-efficient federated framework within the Caribbean, Central, and South America Network for HIV epidemiology. Virologic failure and major regimen change after antiretroviral therapy initiation were analyzed as separate outcomes; for each, we estimated cumulative incidence functions (CIFs) and fit stratified cause-specific Cox proportional hazards models via a surrogate likelihood-based federated implementation. Each site imputed missing data, conducted local analysis, and shared only summary statistics according to a coordinated computation protocol. The federated approach exactly reproduced centralized CIFs and closely approximated centralized Cox regression estimates, outperforming conventional meta-analysis for both outcomes. These findings demonstrate that authentic federated analysis is feasible for multinational HIV research and can yield results closely aligned with centralized analysis while preserving data privacy. Post-hoc feedback from local analysts, however, indicated that broader adoption will require managing the logistical and coordination overhead and ensuring harmonized data collection and quality control across sites.

stat.AP

Overcoming data challenges through enriched validation and targeted sampling to measure whole-person health in electronic health records

The allostatic load index (ALI) is a 10-component measure of whole-person health. Data from electronic health records (EHR) present a huge opportunity to operationalize the ALI in learning health systems; however, these data are prone to missingness and errors. Validation (e.g., through chart reviews) provides better-quality data, but realistically, only a subset of patients' data can be validated, and most protocols do not recover missing data. Using a representative sample of 1000 patients from the EHR at an extensive learning health system (100 of whom could be validated), we propose methods to design, conduct, and analyze statistically efficient and robust studies of ALI and healthcare utilization. Employing semiparametric maximum likelihood estimation, we robustly incorporate all available patient information into statistical models. Using targeted design strategies, we examine ways to select the most informative patients for validation. Incorporating clinical expertise, we devise a novel validation protocol to promote EHR data quality and completeness. Chart reviews uncovered few errors (99% matched source documents) and recovered some missing data through auxiliary information in patients' charts. On average, validation increased the number of non-missing ALI components per patient from 6 to 7. Through simulations based on preliminary data, residual sampling was identified as the most informative strategy for completing our validation study. Incorporating validation data, statistical models indicated that worse whole-person health (higher ALI) was associated with higher odds of engaging in the healthcare system, adjusting for age.

stat.ME

Analysis of Error-prone Electronic Health Records with Multi-wave Validation Sampling: Association of Maternal Weight Gain during Pregnancy with Childhood Outcomes

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, multi-wave, 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 multi-wave 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 6 sampling waves. Estimated associations between childhood obesity/asthma and maternal weight gain, as well as other covariates, are compared to naive 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.

stat.AP