Key result
ClinicalT5 with MC Dropout yields top discrimination for in-hospital mortality, reaching ~0.40 AUPRC.
Why the study?
Existing transformer approaches for clinical prediction focus narrowly on ICU cohorts, rely on hard-to-harmonize multimodal inputs, and rarely provide calibrated uncertainty suitable for triage.
Does uncertainty-calibrated adaptation of clinical transformer foundation models improve the prediction of in-hospital mortality and 30-day readmission in general hospital admissions?
Observational
No
Does uncertainty-calibrated adaptation of clinical transformer foundation models improve the prediction of in-hospital mortality and 30-day readmission in general hospital admissions?
Procedure-code sequences paired with uncertainty-calibrated parameter-efficient adaptation of clinical transformers can support reliable risk estimates for in-hospital mortality and readmission across general hospital admissions.
Supports uncertainty-aware transformers for mortality/readmission risk in general admissions; leaves open prospective validation before practice change.
Accurate prediction of in-hospital mortality and 30-day readmission is important for clinical decision support, yet existing transformer approaches focus narrowly on ICU cohorts, rely on multimodal inputs that few institutions can harmonize, and rarely provide calibrated uncertainty suitable for triage. We address these gaps with a portability-first design, studying the broad general hospital admission population—spanning both ICU and general ward patients—using only ICD procedure code sequences combined with age and sex. This minimal, universally recorded input is itself a contribution, yielding a model substrate that is interoperable, auditable, and applicable to resource-constrained settings. On this foundation, we conduct the first systematic comparison of uncertainty-aware parameter-efficient adaptation strategies for clinical transformer foundation models on general admissions, evaluating full-parameter fine-tuning, Single LoRA, LoRA Ensemble, Bayesian LoRA, and Monte Carlo Dropout against classical baselines, with a leakage-aware mortality protocol on MIMIC-IV and external validation on MIMIC-III. Our analysis shows that no single uncertainty mechanism dominates: stochastic averaging on a fully fine-tuned backbone delivers the strongest discrimination, Bayesian adaptation is best calibrated on the highly imbalanced mortality outcome, and ensemble averaging is best calibrated on the more heterogeneous readmission outcome, while the clinical transformer generalizes more gracefully than classical baselines under domain shift. Together, these findings establish that procedure-code sequences alone, paired with uncertainty-calibrated parameter-efficient adaptation, can support reliable, deployment-ready risk estimates across the general hospital admission population, and clarify how to match the uncertainty mechanism to outcome prevalence and clinical objective.
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Chung et al. (2026) conducted an observational in General hospital admission (in-hospital mortality and 30-day readmission). ClinicalT5 with uncertainty-calibrated parameter-efficient adaptation (MC Dropout, Bayesian LoRA, LoRA Ensemble) vs. Classical baselines (Logistic Regression, XGBoost) and full-parameter fine-tuning was evaluated on In-hospital mortality and 30-day readmission prediction performance (AUPRC, AUROC, ECE, NLL). ClinicalT5-Large with Monte Carlo Dropout achieved the strongest discrimination for in-hospital mortality (AUPRC 0.4016) and 30-day readmission, while Bayesian LoRA provided the best calibration for mortality.
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