Abstract / Summary
Background: Patients with intracerebral hemorrhage (ICH) in intensive care units (ICUs) frequently receive antibiotics early in critical illness. Such exposure reflects suspected infection, physiological deterioration, monitoring intensity, and clinical management and may vary across institutions and electronic health record databases. We evaluated target-domain adaptation for modeling sustained antibiotic exposure in critically ill patients with ICH. Methods: We analyzed derived ICH cohorts from MIMIC-IV and the eICU Collaborative Research Database. MIMIC-IV included 2,024 ICU stays and served as the source cohort. The eICU cohort comprised 1,277 stays and was divided, at the ICU-stay level, into a development subset (766 stays) and a held-out evaluation subset (511 stays). The eICU outcome was sustained antibiotic exposure on at least two ICU days. Candidate models incorporated demographic, comorbidity, physiological, laboratory, neurologic, respiratory, temporal, and measurement-process features. Timestamped observations for static and temporal tabular families were censored at the recorded first-antibiotic time when available, whereas the compact sequence component and explicit measurement-density features used the full first 24 hours. For base-model families using eICU development data, meta-learner inputs were generated by five-fold stratified cross-fitting. A 42-input L2-penalized logistic meta-learner combined 16 model probabilities with model-summary, clinical, availability, and measurement-density features. Results: The held-out eICU subset contained 48 positive outcomes (9.39%). The adapted ensemble achieved an area under the receiver operating characteristic curve (AUROC) of 0.841 (95% CI 0.775-0.899) and an average precision (AP) of 0.540 (95% CI 0.399-0.676), with a Brier score of 0.063 and expected calibration error of 0.029. The MIMIC-IV source-only stack achieved an AUROC of 0.782; the paired AUROC difference was 0.059 (95% CI 0.003-0.112). In a separate patient-grouped five-fold out-of-fold sensitivity analysis of 503 linked eICU stays, AUROC was 0.807 (95% CI 0.691-0.910). Conclusions: Target-domain adaptation improved held-out discrimination relative to a source-only stack for sustained antibiotic exposure. Because some model components and measurement-process features used information from the broader first 24 hours, the model should be interpreted as a first-24-hour treatment-association model rather than a strictly prospective pre-treatment infection predictor.