Clinical decision support using heterogeneous electronic health records (EHRs) is a well-established yet rapidly expanding research area. Large language model (LLM)-driven approaches have shown dominant performance in processing unstructured data such as clinical notes for disease phenotype classification. However, the absence of a unified reasoning framework capable of integrating structured laboratory results with unstructured clinical notes under zero-shot conditions limits progress in multimodal clinical decision support. To address this gap, we propose MediPhen, a novel reasoning framework that transfers LLMs for multi-morbidity disease phenotyping using multimodal clinical data. MediPhen introduces a framework for adapting LLMs to zero-shot disease phenotyping by incorporating extracted clinical entities, their relations, and lab narratives from EHRs, integrating a clinical knowledgebase to guide phenotype classification and enhance LLM transfer learning performance, and an explanation module that leverages chain-of-thought prompting to improve clinical reasoning. Comprehensive experiments conducted on MIMIC-III and MIMIC-IV benchmarks across multiple LLMs demonstrate the effectiveness of MediPhen. Notably, MedGemma-27B achieved state-of-the-art performance, improving micro averaged F1 scores by 19.92% on MIMIC-III and 16.68% on MIMIC-IV compared to fine-tuned baselines. These results highlight MediPhen as a zero-shot screening tool for multi morbidity phenotype classification, scalable within research infrastructures, advancing integration of structured and unstructured EHR data in clinical AI.
Priyadarshana et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: