Abstract

BackgroundA spectrum effect was defined as differences in the sensitivity or specificity of a diagnostic test according to the patient's characteristics or disease features. A spectrum effect can lead to a spectrum bias when subgroup variations in sensitivity or specificity also affect the likelihood ratios and thus post-test probabilities. We propose and illustrate a methodological framework to distinguish spectrum effects from spectrum biases.MethodsData were collected for 1781 women having had a cervical smear test and colposcopy followed by biopsy if abnormalities were detected (the reference standard). Logistic models were constructed to evaluate both the sensitivity and specificity, and the likelihood ratios, of the test and to identify factors independently affecting the test's characteristics.ResultsFor both tests, human papillomavirus test, study setting and age affected sensitivity or specificity of the smear test (spectrum effect), but only human papillomavirus test and study setting modified the likelihood ratios (spectrum bias) for clinical reading, whereas only human papillomavirus test and age modified the likelihood ratios (spectrum bias) for "optimized" interpretation.ConclusionFitting sensitivity, specificity and likelihood ratios simultaneously allows the identification of covariates that independently affect diagnostic or screening test results and distinguishes spectrum effect from spectrum bias. We recommend this approach for the development of new tests, and for reporting test accuracy for different patient populations.

Highlights

  • A spectrum effect was defined as differences in the sensitivity or specificity of a diagnostic test according to the patient's characteristics or disease features

  • Data sources We undertook a secondary analysis of the study by the French Society of Clinical Cytology to compare the efficiency of the conventional Papanicolaou smear, ThinPrep liquid-based cytology and the Hybrid-Capture II human papillomavirus test (HPV test) [24,25,26]

  • All women included in this study (n = 1781) were evaluated by the reference standard, by the index test and by the HPV test

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Summary

Methods

Data were collected for 1781 women having had a cervical smear test and colposcopy followed by biopsy if abnormalities were detected (the reference standard). All women included in this study (n = 1781) were evaluated by the reference standard (colposcopy followed by biopsy if abnormalities were detected), by the index test (conventional Papanicolaou smear test) and by the HPV test (which was considered in this analysis as a "spectrum" variable). These women were either referred for colposcopy because abnormalities had been detected on previous smears (referral clinic setting, n = 461) or were attending for routine smears (screening setting, n = 1320). Other characteristics of the women were recorded: age, current smoking, European or http://www.biomedcentral.com/1471-2288/8/7 other origin, educational level, menopausal status and contraception status

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