Assessing the practice of data quality evaluation in a national clinical data research network through a systematic scoping review in the era of real-world data

Author:

Bian Jiang12ORCID,Lyu Tianchen1,Loiacono Alexander1,Viramontes Tonatiuh Mendoza1,Lipori Gloria3,Guo Yi1,Wu Yonghui1,Prosperi Mattia4ORCID,George Thomas J5ORCID,Harle Christopher A1,Shenkman Elizabeth A1,Hogan William1ORCID

Affiliation:

1. Department of Health Outcomes and Biomedical Informatics, College of Medicine, University of Florida, Gainesville, Florida, USA

2. Cancer Informatics Shared Resource, University of Florida Health Cancer Center, Gainesville, Florida, USA

3. Clinical and Translational Institute, University of Florida, Gainesville, Florida, USA

4. Department of Epidemiology, College of Public Health and Health Professions & College of Medicine, University of Florida, Gainesville, Florida, USA

5. Hematology & Oncology, Department of Medicine, College of Medicine, University of Florida, Gainesville, Florida, USA

Abstract

Abstract Objective To synthesize data quality (DQ) dimensions and assessment methods of real-world data, especially electronic health records, through a systematic scoping review and to assess the practice of DQ assessment in the national Patient-centered Clinical Research Network (PCORnet). Materials and Methods We started with 3 widely cited DQ literature—2 reviews from Chan et al (2010) and Weiskopf et al (2013a) and 1 DQ framework from Kahn et al (2016)—and expanded our review systematically to cover relevant articles published up to February 2020. We extracted DQ dimensions and assessment methods from these studies, mapped their relationships, and organized a synthesized summarization of existing DQ dimensions and assessment methods. We reviewed the data checks employed by the PCORnet and mapped them to the synthesized DQ dimensions and methods. Results We analyzed a total of 3 reviews, 20 DQ frameworks, and 226 DQ studies and extracted 14 DQ dimensions and 10 assessment methods. We found that completeness, concordance, and correctness/accuracy were commonly assessed. Element presence, validity check, and conformance were commonly used DQ assessment methods and were the main focuses of the PCORnet data checks. Discussion Definitions of DQ dimensions and methods were not consistent in the literature, and the DQ assessment practice was not evenly distributed (eg, usability and ease-of-use were rarely discussed). Challenges in DQ assessments, given the complex and heterogeneous nature of real-world data, exist. Conclusion The practice of DQ assessment is still limited in scope. Future work is warranted to generate understandable, executable, and reusable DQ measures.

Funder

University of Florida’s Creating the Healthiest Generation—Moonshot

National Institutes of Health

Patient-Centered Outcomes Research Institute

OneFlorida Clinical Research Consortium

Publisher

Oxford University Press (OUP)

Subject

Health Informatics

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