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Empirical evidence of design-related bias in studies of diagnostic tests.

Authors :
Lijmer, Jeroen G.
Mol, Ben Willem
Lijmer, J G
Mol, B W
Heisterkamp, S
Bonsel, G J
Prins, M H
van der Meulen, J H
Bossuyt, P M
Source :
JAMA: Journal of the American Medical Association; 9/15/99, Vol. 282 Issue 11, p1061-1066, 6p, 2 Charts, 1 Graph
Publication Year :
1999

Abstract

<bold>Context: </bold>The literature contains a large number of potential biases in the evaluation of diagnostic tests. Strict application of appropriate methodological criteria would invalidate the clinical application of most study results.<bold>Objective: </bold>To empirically determine the quantitative effect of study design shortcomings on estimates of diagnostic accuracy.<bold>Design and Setting: </bold>Observational study of the methodological features of 184 original studies evaluating 218 diagnostic tests. Meta-analyses on diagnostic tests were identified through a systematic search of the literature using MEDLINE, EMBASE, and DARE databases and the Cochrane Library (1996-1997). Associations between study characteristics and estimates of diagnostic accuracy were evaluated with a regression model.<bold>Main Outcome Measures: </bold>Relative diagnostic odds ratio (RDOR), which compared the diagnostic odds ratios of studies of a given test that lacked a particular methodological feature with those without the corresponding shortcomings in design.<bold>Results: </bold>Fifteen (6.8%) of 218 evaluations met all 8 criteria; 64 (30%) met 6 or more. Studies evaluating tests in a diseased population and a separate control group overestimated the diagnostic performance compared with studies that used a clinical population (RDOR, 3.0; 95% confidence interval [CI], 2.0-4.5). Studies in which different reference tests were used for positive and negative results of the test under study overestimated the diagnostic performance compared with studies using a single reference test for all patients (RDOR, 2.2; 95% CI, 1.5-3.3). Diagnostic performance was also overestimated when the reference test was interpreted with knowledge of the test result (RDOR, 1.3; 95% CI, 1.0-1.9), when no criteria for the test were described (RDOR, 1.7; 95% CI, 1.1-2.5), and when no description of the population under study was provided (RDOR, 1.4; 95% CI, 1.1-1.7).<bold>Conclusion: </bold>These data provide empirical evidence that diagnostic studies with methodological shortcomings may overestimate the accuracy of a diagnostic test, particularly those including nonrepresentative patients or applying different reference standards. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00987484
Volume :
282
Issue :
11
Database :
Complementary Index
Journal :
JAMA: Journal of the American Medical Association
Publication Type :
Academic Journal
Accession number :
2411791
Full Text :
https://doi.org/10.1001/jama.282.11.1061