A span-based model for extracting overlapping PICO entities from randomized controlled trial publications.

TitleA span-based model for extracting overlapping PICO entities from randomized controlled trial publications.
Publication TypeJournal Article
Year of Publication2024
AuthorsZhang G, Zhou Y, Hu Y, Xu H, Weng C, Peng Y
JournalJ Am Med Inform Assoc
Volume31
Issue5
Pagination1163-1171
Date Published2024 Apr 19
ISSN1527-974X
KeywordsAlzheimer Disease, COVID-19, Humans, Natural Language Processing
Abstract

OBJECTIVES: Extracting PICO (Populations, Interventions, Comparison, and Outcomes) entities is fundamental to evidence retrieval. We present a novel method, PICOX, to extract overlapping PICO entities.

MATERIALS AND METHODS: PICOX first identifies entities by assessing whether a word marks the beginning or conclusion of an entity. Then, it uses a multi-label classifier to assign one or more PICO labels to a span candidate. PICOX was evaluated using 1 of the best-performing baselines, EBM-NLP, and 3 more datasets, ie, PICO-Corpus and randomized controlled trial publications on Alzheimer's Disease (AD) or COVID-19, using entity-level precision, recall, and F1 scores.

RESULTS: PICOX achieved superior precision, recall, and F1 scores across the board, with the micro F1 score improving from 45.05 to 50.87 (P ≪.01). On the PICO-Corpus, PICOX obtained higher recall and F1 scores than the baseline and improved the micro recall score from 56.66 to 67.33. On the COVID-19 dataset, PICOX also outperformed the baseline and improved the micro F1 score from 77.10 to 80.32. On the AD dataset, PICOX demonstrated comparable F1 scores with higher precision when compared to the baseline.

CONCLUSION: PICOX excels in identifying overlapping entities and consistently surpasses a leading baseline across multiple datasets. Ablation studies reveal that its data augmentation strategy effectively minimizes false positives and improves precision.

DOI10.1093/jamia/ocae065
Alternate JournalJ Am Med Inform Assoc
PubMed ID38471120
PubMed Central IDPMC11031223
Grant ListR01 LM014344 / LM / NLM NIH HHS / United States
UL1 TR001873 / TR / NCATS NIH HHS / United States
R01LM009886 / LM / NLM NIH HHS / United States