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Abstract Number: 1148

Evaluation of a Methodological Approach to Determine Timing of Rheumatoid Arthritis Disease Onset Using Administrative Claims Data

Jie Zhang1, Fenglong Xie2, Lang Chen3, Jeffrey D. Greenberg4 and Jeffrey R. Curtis5, 1Ryals Soph Bldg., Rm. 517b, Univ. of Alabama at Birmingham, Birmingham, AL, 2Rheumatology & Immunology, University of Alabama at Birmingham, Birmingham, AL, 3Medicine, University of Alabama at Birmingham, Birmingham, AL, 4Rheumatology, New York University School of Medicine, New York, NY, 5University of Alabama at Birmingham, Birmingham, AL

Meeting: 2014 ACR/ARHP Annual Meeting

Keywords: Administrative databases and rheumatoid arthritis (RA)

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Session Information

Title: Health Services Research

Session Type: Abstract Submissions (ACR)

Background/Purpose: The identification of patients with recent-onset rheumatoid arthritis (RA) is often desirable to create inception cohorts of patients.  We evaluated an approach to identify the timing of RA onset using administrative claims data from public (Medicare) and commercial health plans.

Methods: The study sample consisted of RA patients participating in Corrona, a large North American RA registry, linked to administrative medical and pharmacy claims data from Medicare (2006 to 2011) or a U.S. commercial health plan (2005-2012). We estimated year of RA onset in the claims data using several algorithms that were based on the following factors: 1) different ICD-9 diagnosis code for RA (e.g. 714.0, 714.2, and 714.81. vs. 714.X, code from physician visit claim vs. any claim); and 2) length of observable time in the health plan (>1 vs. > 2 years) preceding the first diagnosis code for RA, with exclusions for use of any disease modifying anti-rheumatic drugs.  We compared the estimated year of RA onset using the claims-based algorithms to that recorded by rheumatologists in the Corrona registry (gold standard).  We reported accuracy as a positive predictive value (PPV), calculated if the year of RA onset from the claims data agreed (+- 1 year) with that documented in Corrona. We conducted a subgroup analysis limited to patients whose disease duration was 2 years or less at their first Corrona rheumatologist visit to improve the reliability of disease onset ascertainment by reducing recall bias and misclassification of the gold standard. 

Results:  In the main analysis, using ICD-9 codes 714.0, 714.2, 714.81 from a physician visit, the PPVs for accurately classifying year of RA onset ranged from 62% to 68%. When ICD-9 codes 714.x from any type of claim were used, PPVs were higher, ranging from 67% to 100%. In subgroup analysis of patients with more recently diagnosed RA, PPVs were much higher, ranging from 91-100%.

Conclusion: Claims-based algorithms can be used with high validity to identify patients with recent onset RA.  Additional research will focus on reasons and opportunities to reduce misclassification of disease onset.


Table: PPVs of claims-based algorithms to identify recent onset RA compared to gold standard of rheumatologist report

 

 

Medicare

Commercial Health Plan

Claims-Based Algorithm

Look Back Period

Total N

PPV

Total N

PPV

All Patients

714.0, 714.2, 714.21 on physician claim

>=365 days

144

62%

21

67%

>=730 days

84

68%

12

67%

714.xx from any claim

>=365 days

182

67%

34

71%

>=730 days

93

77%

12

100%

 

Patients with year of RA diagnosis within 2 years from time of physician ascertainment*

714.0, 714.2, 714.21 on physician claim

>=365 days

120

91%

24

100%

>=730 days

80

91%

15

100%

714.xx from any claim

>=365 days

139

94%

22

91%

>=730 days

73

92%

15

93%

*The purpose of the subgroup analysis is to identify patients whose year of onset is less likely to be biased due to recalling events occurred a long time ago


Disclosure:

J. Zhang,
None;

F. Xie,
None;

L. Chen,
None;

J. D. Greenberg,

Corrona, LLC.,

1,

Corrona, LLC.,

3,

AstraZeneca, Celgene, Novartis and Pfizer,

5;

J. R. Curtis,

Roche, Genentech, UCB Pharma, Janssen, CORRONA, Amgen, Pfizer, BMS, Crescendo, AbbVie,

2,

Roche, Genentech, UCB Pharma, Janssen, CORRONA, Amgen, Pfizer, BMS, Crescendo, AbbVie,

5.

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