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Generalizable and Scalable Multistage Biomedical Concept Normalization Leveraging Large Language Models

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arxiv 2405.15122 v1 pith:4QMGSIQR submitted 2024-05-24 cs.CL

classification cs.CL
keywords normalizationbiomedicallanguagellmsopen-sourcebetabm25concept
verification ladder T0 review T1 audit T2 compute T3 formal
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abstract

Background: Biomedical entity normalization is critical to biomedical research because the richness of free-text clinical data, such as progress notes, can often be fully leveraged only after translating words and phrases into structured and coded representations suitable for analysis. Large Language Models (LLMs), in turn, have shown great potential and high performance in a variety of natural language processing (NLP) tasks, but their application for normalization remains understudied. Methods: We applied both proprietary and open-source LLMs in combination with several rule-based normalization systems commonly used in biomedical research. We used a two-step LLM integration approach, (1) using an LLM to generate alternative phrasings of a source utterance, and (2) to prune candidate UMLS concepts, using a variety of prompting methods. We measure results by $F_{\beta}$, where we favor recall over precision, and F1. Results: We evaluated a total of 5,523 concept terms and text contexts from a publicly available dataset of human-annotated biomedical abstracts. Incorporating GPT-3.5-turbo increased overall $F_{\beta}$ and F1 in normalization systems +9.5 and +7.3 (MetaMapLite), +13.9 and +10.9 (QuickUMLS), and +10.5 and +10.3 (BM25), while the open-source Vicuna model achieved +10.8 and +12.2 (MetaMapLite), +14.7 and +15 (QuickUMLS), and +15.6 and +18.7 (BM25). Conclusions: Existing general-purpose LLMs, both propriety and open-source, can be leveraged at scale to greatly improve normalization performance using existing tools, with no fine-tuning.

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    LLM agents given abstracts, methods, and data dictionary entries approximately reproduced about 53% of key abstract findings across five Alzheimer's disease studies, with frequent mismatches in statistical methods.

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