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Katrina Poppe

Publications and source records attributed to Katrina Poppe.

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From Statistical Fidelity to Clinical Consistency: Scalable Generation and Auditing of Synthetic Patient Trajectories

Access to electronic health records (EHRs) for digital health research is often limited by privacy regulations and institutional barriers. Synthetic EHRs have been proposed as a way to enable safe and sovereign data sharing; however, existing methods may produce records that capture overall statistical properties of real data but present inconsistencies across clinical processes and observations. We developed an integrated pipeline to make synthetic patient trajectories clinically consistent through two synergistic steps: high-fidelity generation and scalable auditing. Using the MIMIC-IV database, we trained a knowledge-grounded generative model that represents nearly 32,000 distinct clinical events, including demographics, laboratory measurements, medications, procedures, and diagnoses, while enforcing structural integrity. To support clinical consistency at scale, we incorporated an automated auditing module leveraging large language models to filter out clinical inconsistencies (e.g., contraindicated medications) that escape probabilistic generation. We generated 18,071 synthetic patient records derived from a source cohort of 180,712 real patients. While synthetic clinical event probabilities demonstrated robust agreement (mean bias effectively 0.00) and high correlation (R2=0.99) with the real counterparts, review of a random sample of synthetic records (N=20) by three clinicians identified inconsistencies in 45-60% of them. Automated auditing reduced the difference between real and synthetic data (Cohen's effect size d between 0.59 and 1.60 before auditing, and between 0.18 and 0.67 after auditing). Downstream models trained on audited data matched or even exceeded real-data performance. We found no evidence of privacy risks, with membership inference performance indistinguishable from random guessing (F1-score=0.51).

cs.LG

Predicting cardiovascular risk from national administrative databases using a combined survival analysis and deep learning approach

AIMS. This study compared the performance of deep learning extensions of survival analysis models with traditional Cox proportional hazards (CPH) models for deriving cardiovascular disease (CVD) risk prediction equations in national health administrative datasets. METHODS. Using individual person linkage of multiple administrative datasets, we constructed a cohort of all New Zealand residents aged 30-74 years who interacted with publicly funded health services during 2012, and identified hospitalisations and deaths from CVD over five years of follow-up. After excluding people with prior CVD or heart failure, sex-specific deep learning and CPH models were developed to estimate the risk of fatal or non-fatal CVD events within five years. The proportion of explained time-to-event occurrence, calibration, and discrimination were compared between models across the whole study population and in specific risk groups. FINDINGS. First CVD events occurred in 61,927 of 2,164,872 people. Among diagnoses and procedures, the largest 'local' hazard ratios were associated by the deep learning models with tobacco use in women (2.04, 95%CI: 1.99-2.10) and with chronic obstructive pulmonary disease with acute lower respiratory infection in men (1.56, 95%CI: 1.50-1.62). Other identified predictors (e.g. hypertension, chest pain, diabetes) aligned with current knowledge about CVD risk predictors. The deep learning models significantly outperformed the CPH models on the basis of proportion of explained time-to-event occurrence (Royston and Sauerbrei's R-squared: 0.468 vs. 0.425 in women and 0.383 vs. 0.348 in men), calibration, and discrimination (all p<0.0001). INTERPRETATION. Deep learning extensions of survival analysis models can be applied to large health administrative databases to derive interpretable CVD risk prediction equations that are more accurate than traditional CPH models.

cs.LG