Abstract:Survival analysis is a fundamental tool for modeling time-to-event outcomes in healthcare. Recent advances have introduced flexible neural network approaches for improved predictive performance. However, most of these models do not provide interpretable insights into the association between exposures and the modeled outcomes, a critical requirement for decision-making in clinical practice. To address this limitation, we propose Additive Deep Hazard Analysis Mixtures (ADHAM), an interpretable additive survival model. ADHAM assumes a conditional latent structure that defines subgroups, each characterized by a combination of covariate-specific hazard functions. To select the number of subgroups, we introduce a post-training refinement that reduces the number of equivalent latent subgroups by merging similar groups. We perform comprehensive studies to demonstrate ADHAM's interpretability at the population, subgroup, and individual levels. Extensive experiments on real-world datasets show that ADHAM provides novel insights into the association between exposures and outcomes. Further, ADHAM remains on par with existing state-of-the-art survival baselines in terms of predictive performance, offering a scalable and interpretable approach to time-to-event prediction in healthcare.
Abstract:Sex and gender-based healthcare disparities contribute to differences in health outcomes. We focus on time to diagnosis (TTD) by conducting two large-scale, complementary analyses among men and women across 29 phenotypes and 195K patients. We first find that women are consistently more likely to experience a longer TTD than men, even when presenting with the same conditions. We further explore how TTD disparities affect diagnostic performance between genders, both across and persistent to time, by evaluating gender-agnostic disease classifiers across increasing diagnostic information. In both fairness analyses, the diagnostic process favors men over women, contradicting the previous observation that women may demonstrate relevant symptoms earlier than men. These analyses suggest that TTD is an important yet complex aspect when studying gender disparities, and warrants further investigation.