Comparison of a brush-sampling fecal immunochemical test for hemoglobin with a sensitive guaiac-based fecal occult blood test in detection of colorectal neoplasia
β Scribed by Robert H. Fletcher; David F. Ransohoff; Thomas F. Imperiale
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 39 KB
- Volume
- 109
- Category
- Article
- ISSN
- 0008-543X
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β¦ Synopsis
Comparison of a Brush-sampling Fecal Immunochemical Test for Hemoglobin With a Sensitive Guaiac-based Fecal Occult Blood Test in Detection of Colorectal Neoplasia S mith et al. 1 compared the performance of a fecal immunochem- ical test (FIT) for hemoglobin to a sensitive, guaiac-based fecal occult blood test (GFOBT) in a large cohort of average-risk adults and found that the FIT was more sensitive for cancers and significant adenomas. They report that ''. . .the FIT returned a true-positive result. . .in cancer. . .[of] 87.5%.'' Readers should not mistake this result for the true sensitivity in the usual sense: the proportion of all patients with cancer who have a positive test.
The study by Smith et al was conducted in such a way that true sensitivity is necessarily overestimated and easily can approach 100%. Almost all participants in this study underwent colonoscopy only if 1 of the 2 fecal occult blood tests was positive. Patients with cancer who had negative tests-which would have been counted as false-negative results, causing lower sensitivity-systematically were excluded. This problem, known as diagnostic work-up bias, 2 would have been avoided only by performing colonoscopy on all members of the cohort, regardless of the test results. 3 The extent to which the reported ''true-positive rate'' may have overestimated true sensitivity is illustrated by the following example: The literature suggests that no more than half of colorectal cancers bleed at a given point in time. If so, then at least 48 of the 2512 study participants would have had cancer, not just the 24 that were diagnosed because they bled, causing 1 or both of the tests to be positive. The true sensitivity for FIT then would have been 21 of 48 (43.8%), and not the 21 of 24 (87.5%) reported. Taking into account statistical uncertainty (the 95% confidence interval), sensitivity would have been in the 29% to 58% range. The ''true positive rate'' used for comparing 2 tests within a study like the one by Smith et al 1 is not a valid estimate of true sensitivity for comparison with the sensitivities of other tests reported in the literature.
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