Phenonizer: A Fine-Grained Phenotypic Named Entity Recognizer for Chinese Clinical Texts

Author:

Zou Qunsheng1ORCID,Yang Kuo1ORCID,Shu Zixin1ORCID,Chang Kai1ORCID,Zheng Qiguang1ORCID,Zheng Yi1,Lu Kezhi1ORCID,Xu Ning2,Tian Haoyu1,Li Xiaomeng1,Yang Yuxia1,Zhou Yana3,Yu Haibin2,Zhang Xiaoping4,Xia Jianan1ORCID,Zhu Qiang1ORCID,Poon Josiah5,Poon Simon5,Zhang Runshun6ORCID,Li Xiaodong37ORCID,Zhou Xuezhong1ORCID

Affiliation:

1. Institute of Medical Intelligence, School of Computer and Information Technology, Beijing Jiaotong University, Beijing 100044, China

2. The First Affiliated Hospital of Henan University of Chinese Medicine, Zhengzhou 45000, China

3. Hubei Provincial Hospital of Traditional Chinese Medicine, Wuhan 430061, China

4. Data Centre of Traditional Chinese Medicine, China Academy of Chinese Medical Science, Beijing 100700, China

5. School of Information Technologies, The University of Sydney, Sydney, Australia, Analytic and Clinical Cooperative Laboratory for Integrative Medicine, USYD & CUHK, Sydney 2006, Australia

6. Guang’anmen Hospital, China Academy of Chinese Medical Science, Beijing 100053, China

7. Institute of Liver Disease, Hubei Provincial Academy of Traditional Chinese Medicine, Wuhan 430061, China

Abstract

Biomedical named entity recognition (BioNER) from clinical texts is a fundamental task for clinical data analysis due to the availability of large volume of electronic medical record data, which are mostly in free text format, in real-world clinical settings. Clinical text data incorporates significant phenotypic medical entities (e.g., symptoms, diseases, and laboratory indexes), which could be used for profiling the clinical characteristics of patients in specific disease conditions (e.g., Coronavirus Disease 2019 (COVID-19)). However, general BioNER approaches mostly rely on coarse-grained annotations of phenotypic entities in benchmark text dataset. Owing to the numerous negation expressions of phenotypic entities (e.g., “no fever,” “no cough,” and “no hypertension”) in clinical texts, this could not feed the subsequent data analysis process with well-prepared structured clinical data. In this paper, we developed Human-machine Cooperative Phenotypic Spectrum Annotation System (http://www.tcmai.org/login, HCPSAS) and constructed a fine-grained Chinese clinical corpus. Thereafter, we proposed a phenotypic named entity recognizer: Phenonizer, which utilized BERT to capture character-level global contextual representation, extracted local contextual features combined with bidirectional long short-term memory, and finally obtained the optimal label sequences through conditional random field. The results on COVID-19 dataset show that Phenonizer outperforms those methods based on Word2Vec with an F1-score of 0.896. By comparing character embeddings from different data, it is found that character embeddings trained by clinical corpora can improve F -score by 0.0103. In addition, we evaluated Phenonizer on two kinds of granular datasets and proved that fine-grained dataset can boost methods’ F1-score slightly by about 0.005. Furthermore, the fine-grained dataset enables methods to distinguish between negated symptoms and presented symptoms. Finally, we tested the generalization performance of Phenonizer, achieving a superior F1-score of 0.8389. In summary, together with fine-grained annotated benchmark dataset, Phenonizer proposes a feasible approach to effectively extract symptom information from Chinese clinical texts with acceptable performance.

Funder

China Academy of Chinese Medical Sciences

Publisher

Hindawi Limited

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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