Validity of administrative data for the diagnosis of primary sclerosing cholangitis: a population-based study

被引:19
|
作者
Molodecky, Natalie A. [2 ,3 ]
Myers, Robert P. [2 ,3 ]
Barkema, Herman W. [3 ,4 ]
Quan, Hude [3 ]
Kaplan, Gilaad G. [1 ,2 ,3 ]
机构
[1] Univ Calgary, Dept Med, Teaching Res & Wellness Ctr, Calgary, AB T2N 4N1, Canada
[2] Univ Calgary, Div Gastroenterol, Calgary, AB T2N 4N1, Canada
[3] Univ Calgary, Dept Community Hlth Sci, Calgary, AB T2N 4N1, Canada
[4] Univ Calgary, Dept Prod Anim Hlth, Calgary, AB T2N 4N1, Canada
关键词
algorithms; positive predictive value; primary sclerosing cholangitis; sensitivity; validation; INFLAMMATORY-BOWEL-DISEASE; PRIMARY BILIARY-CIRRHOSIS; LIVER-TRANSPLANTATION; AUTOIMMUNE HEPATITIS; ULCERATIVE-COLITIS; EPIDEMIOLOGY; PREVALENCE; EXPERIENCE; OUTCOMES; CHILDREN;
D O I
10.1111/j.1478-3231.2011.02484.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: Administrative databases could be useful in studying the epidemiology of primary sclerosing cholangitis (PSC); however, there is no information regarding the validity of the diagnostic code in administrative databases. The aims of this study were to determine the validity of administrative data for a diagnosis of PSC and generate algorithms for the identification of PSC patients. Methods: The sensitivity (Se) and positive predictive value (PPV) of a PSC diagnosis based on administrative data from 2000 to 2003 were determined through chart review data. Algorithms were developed by considering variables associated with PSC and coding details. A logistic regression model was constructed using covariates associated with PSC. Based on this model, each subject was assigned a probability of having PSC. A cutoff value was selected that maximized the Se and specificity (Sp) of correctly predicting PSC cases. Results: In the administrative data, the initial Se and PPV were 83.7 and 7.2% respectively. The optimal algorithm included one PSC code and one inflammatory bowel disease code and had Se 56% and PPV 59%. Overall, the algorithms yielded inadequate PPV and Se estimates to identify a cohort of true PSC cases. The predictive model was constructed using six covariates. For this model, the area under the receiver operating characteristic curve was 93.5%. A cutoff of 0.0729 was used, which maximized the Se 81.9% and Sp 90.7%; however, the PPV was 41.0%. Conclusion: An algorithm for the identification of true PSC cases from administrative data was not possible. We recommend that PSC receives a distinct ICD code from ascending cholangitis.
引用
收藏
页码:712 / 720
页数:9
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