Literature DB >> 32470694

Converting clinical document architecture documents to the common data model for incorporating health information exchange data in observational health studies: CDA to CDM.

Hyerim Ji1, Seok Kim1, Soyoung Yi1, Hee Hwang2, Jeong-Whun Kim3, Sooyoung Yoo4.   

Abstract

BACKGROUND: Utilization of standard health information exchange (HIE) data is growing due to the high adoption rate and interoperability of electronic health record (EHR) systems. However, integration of HIE data into an EHR system is not yet fully adopted in clinical research. In addition, data quality should be verified for the secondary use of these data. Thus, the aims of this study were to convert referral documents in a Health Level 7 (HL7) clinical document architecture (CDA) to the common data model (CDM) to facilitate HIE data availability for longitudinal data analysis, and to identify data quality levels for application in future clinical studies.
METHODS: A total of 21,492 referral CDA documents accumulated for over 10 years in a tertiary general hospital in South Korea were analyzed. To convert CDA documents to the Observational Medical Outcomes Partnership (OMOP) CDM, processes such as CDA parsing, data cleaning, standard vocabulary mapping, CDA-to-CDM mapping, and CDM conversion were performed. The quality of CDM data was then evaluated using the Achilles Heel and visualized with the Achilles tool.
RESULTS: Mapping five CDA elements (document header, problem, medication, laboratory, and procedure) into an OMOP CDM table resulted in population of 9 CDM tables (person, visit_occurrence, condition_occurrence, drug_exposure, measurement, observation, procedure_occurrence, care_site, and provider). Three CDM tables (drug_era, condition_era, and observation_period) were derived from the converted table. From vocabulary mapping codes in CDA documents according to domain, 98.6% of conditions, 68.8% of drugs, 35.7% of measurements, 100% of observation, and 56.4% of procedures were mapped as standard concepts. The conversion rates of the CDA to the OMOP CDM were 96.3% for conditions, 97.2% for drug exposure, 98.1% for procedure occurrence, 55.1% for measurements, and 100% for observation.
CONCLUSIONS: We examined the possibility of CDM conversion by defining mapping rules for CDA-to-CDM conversion using the referral CDA documents collected from clinics in actual medical practice. Although mapping standard vocabulary for CDM conversion requires further improvement, the conversion could facilitate further research on the usage patterns of medical resources and referral patterns.
Copyright © 2020 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Clinical document architecture; Common data model; Observational Medical Outcomes Partnership; Referral documents

Mesh:

Year:  2020        PMID: 32470694     DOI: 10.1016/j.jbi.2020.103459

Source DB:  PubMed          Journal:  J Biomed Inform        ISSN: 1532-0464            Impact factor:   6.317


  2 in total

1.  Deep-learning-based automated terminology mapping in OMOP-CDM.

Authors:  Byungkon Kang; Jisang Yoon; Ha Young Kim; Sung Jin Jo; Yourim Lee; Hye Jin Kam
Journal:  J Am Med Inform Assoc       Date:  2021-07-14       Impact factor: 4.497

2.  Existing barriers and recommendations of real-world data standardisation for clinical research in China: a qualitative study.

Authors:  Junkai Lai; Xiwen Liao; Chen Yao; Feifei Jin; Bin Wang; Chen Li; Jun Zhang; Larry Liu
Journal:  BMJ Open       Date:  2022-08-03       Impact factor: 3.006

  2 in total

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