Systematic review of scope and quality of electronic patient record data in primary care

Abstract

Objective: To systematically review measures of data quality in electronic patient records (EPRs) in primary care.

Design: Systematic review of English language publications, 1980-2001.

Data sources: Bibliographic searches of medical databases, specialist medical informatics databases, conference proceedings, and institutional contacts.

Study selection: Studies selected according to a predefined framework for categorising review papers.

Data extraction: Reference standards and measurements used to judge quality.

Results: Bibliographic searches identified 4589 publications. After primary exclusions 174 articles were classified, 52 of which met the inclusion criteria for review. Selected studies were primarily descriptive surveys. Variability in methods prevented meta-analysis of results. Forty eight publications were concerned with diagnostic data, 37 studies measured data quality, and 15 scoped EPR quality. Reliability of data was assessed with rate comparison. Measures of sensitivity were highly dependent on the element of EPR data being investigated, while the positive predictive value was consistently high, indicating good validity. Prescribing data were generally of better quality than diagnostic or lifestyle data.

Conclusion: The lack of standardised methods for assessment of quality of data in electronic patient records makes it difficult to compare results between studies. Studies should present data quality measures with clear numerators, denominators, and confidence intervals. Ambiguous terms such as "accuracy" should be avoided unless precisely defined.