4.2 Article

Validation of claims-based algorithms for identification of high-grade cervical dysplasia and cervical cancer

期刊

PHARMACOEPIDEMIOLOGY AND DRUG SAFETY
卷 22, 期 11, 页码 1239-1244

出版社

WILEY
DOI: 10.1002/pds.3520

关键词

pharmacoepidemiology; cervical dysplasia; cervical cancer; validity; claims data

资金

  1. National Institutes of Health (NIH) [K23 AR059677, K24 AR055989, P60 AR047782, R01 AR056215]
  2. NIH/National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
  3. Informed Medical Decisions Foundation
  4. HMO Research Network Center for Education and Research on Therapeutics (AHRQ) [1U18HS016955-1]
  5. HMO Research Network DEcIDE Center
  6. Agency for Healthcare Research and Quality
  7. NIH/NIAMS
  8. US Food and Drug Administration
  9. [P60 AR 047782]

向作者/读者索取更多资源

BackgroundHigh-grade cervical dysplasia or cervical intraepithelial neoplasia grade 2 or worse has been widely used as a surrogate endpoint in cervical cancer screening or prevention trials. MethodsTo identify high-grade cervical dysplasia and cervical cancer, we developed claims-based algorithms that incorporated a combination of diagnosis and procedure codes using the billing data in an electronic medical records database and assessed the validity of the algorithms in an independent administrative claims database. We calculated the positive predictive value (PPV) with the 95% confidence interval (CI) of each algorithm, using new cytologic or pathologic diagnosis of cervical intraepithelial neoplasia 2 or 3, carcinoma in situ, or cervical cancer as the gold standard. ResultsHaving 1 diagnosis code for high-grade cervical dysplasia or cervical cancer had a PPV of 57.1% (95%CI, 54.7-59.5%). By requiring 2 diagnoses for high-grade cervical dysplasia or cervical cancer, separated by 7-30days, the PPV increased to 60.2% (95%CI, 53.9-66.1%). At least two diagnoses and a procedure code within a month from the first diagnosis date yielded a PPV of 80.7% (95%CI, 73.6-86.2%). The algorithms had greater PPVs in identifying prevalent high-grade cervical dysplasia or cervical cancer. Overall, the PPVs of these algorithms were similar or slightly lower in the external claims data than in the sample used to derive the algorithms. ConclusionsUse of 2 diagnosis codes in combination with a procedure code appears to be a valid tool for studying high-grade cervical dysplasia and cervical cancer in both electronic medical record and administrative claims databases. Copyright (c) 2013 John Wiley & Sons, Ltd.

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