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Identification and validation of lupus nephritis cases using administrative data
L B Chibnik1, E M Massarotti, K H Costenbader
1Division of Rheumatology, Immunology and Allergy, Brigham & Women's Hospital and Harvard Medical School, Boston, MA 02115, USA. lchibnik@rics.bwh.harvard.edu
Identifying patients with lupus nephritis for research is possible using Medicaid billing data. A strategy combining lupus and renal ICD-9 codes with nephrologist claims achieved 88% accuracy.
Area of Science:
- Nephrology
- Health Services Research
- Medical Informatics
Background:
- Large administrative databases like Medicaid claims are valuable for studying rare diseases such as lupus nephritis.
- Accurate patient identification from claims data is crucial for reliable health services research.
Purpose of the Study:
- To develop and validate an algorithm for identifying lupus nephritis cases using ICD-9 billing codes.
- To assess the performance of different coding strategies for lupus nephritis case ascertainment.
Main Methods:
- Compared four ICD-9 code-based strategies to identify lupus nephritis patients from Medicaid data (2000-2007).
- Strategies involved combinations of Systemic Lupus Erythematosus (SLE) codes (ICD-9 710.0), renal ICD-9 codes, and nephrologist visits.
- Validated algorithm performance using positive predictive value (PPV) through medical record review.
Main Results:
- A total of 234 subjects were identified and their medical records reviewed.
- The third strategy, utilizing a combination of lupus and renal ICD-9 codes plus nephrologist encounter claims, demonstrated the highest PPV.
- This optimized strategy achieved an 88% positive predictive value for identifying lupus nephritis patients.
Conclusions:
- A specific algorithm combining lupus and renal ICD-9 codes with nephrologist claims provides a high PPV for identifying lupus nephritis patients.
- This method offers a reliable approach for health services research using administrative claims data.
- The developed strategy can serve as a model for identifying patients with other rare diseases within large datasets.
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