4.5 Article

Assessing the validity of using administrative data to identify patients with epilepsy

期刊

EPILEPSIA
卷 55, 期 2, 页码 335-343

出版社

WILEY
DOI: 10.1111/epi.12506

关键词

Validation; Incidence; Prevalence

资金

  1. Public Health Agency of Canada
  2. ICES
  3. Ontario Ministry of Health and Long-Term Care (MOHLTC)
  4. Canadian Institutes of Health Research (CIHR)
  5. Alberta Innovates Health Solutions (AI-HS)
  6. CIHR
  7. Department of Family and Community Medicine, University of Toronto

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Objective Previous validation studies assessing the use of administrative data to identify patients with epilepsy have used targeted sampling or have used a reference standard of patients in the neurologist, hospital, or emergency room setting. Therefore, the validity of using administrative data to identify patients with epilepsy in the general population has not been previously assessed. The purpose of this study was to determine the validity of using administrative data to identify patients with epilepsy in the general population. Methods A retrospective chart abstraction study was performed using primary care physician records from 83 physicians distributed throughout Ontario and contributing data to the Electronic Medical Record Administrative data Linked Database (EMRALD) A random sample of 7,500 adult patients, from a possible 73,014 eligible, was manually chart abstracted to identify patients who had ever had epilepsy. These patients were used as a reference standard to test a variety of administrative data algorithms. Results An algorithm of three physician billing codes (separated by at least 30days) in 2years or one hospitalization had a sensitivity of 73.7% (95% confidence interval [CI] 64.8-82.5%), specificity of 99.8% (95% CI 99.6-99.9%), positive predictive value (PPV) of 79.5% (95% CI71.1-88.0%), and negative predictive value (NPV) of 99.7% (95% CI99.5-99.8%) for identifying patients who had ever had epilepsy. Significance The results of our study showed that administrative data can reasonably accurately identify patients who have ever had epilepsy, allowing for a lifetime population prevalence determination of epilepsy in Ontario and the rest of Canada with similar administrative databases. This will facilitate future studies on population level patterns and outcomes of care for patients living with epilepsy.

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