The effect of uncertainty in patient classification on diagnostic performance estimations
The performance of a new diagnostic test is typically evaluated against a comparator which is assumed to correspond closely to some true state of interest. Judgments about the new test's performance are based on the differences between the outputs of the test and comparator. It is commonly assu...
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Published in | PloS one Vol. 14; no. 5; p. e0217146 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
United States
Public Library of Science
22.05.2019
Public Library of Science (PLoS) |
Subjects | |
Online Access | Get full text |
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Summary: | The performance of a new diagnostic test is typically evaluated against a comparator which is assumed to correspond closely to some true state of interest. Judgments about the new test's performance are based on the differences between the outputs of the test and comparator. It is commonly assumed that a small amount of uncertainty in the comparator's classifications will negligibly affect the measured performance of a diagnostic test.
Simulated datasets were generated to represent typical diagnostic scenarios. Comparator noise was introduced in the form of random misclassifications, and the effect on the apparent performance of the diagnostic test was determined. An actual dataset from a clinical trial on a new diagnostic test for sepsis was also analyzed.
We demonstrate that as little as 5% misclassification of patients by the comparator can be enough to statistically invalidate performance estimates such as sensitivity, specificity and area under the receiver operating characteristic curve, if this uncertainty is not measured and taken into account. This distortion effect is found to increase non-linearly with comparator uncertainty, under some common diagnostic scenarios. For clinical populations exhibiting high degrees of classification uncertainty, failure to measure and account for this effect will introduce significant risks of drawing false conclusions. The effect of classification uncertainty is magnified further for high performing tests that would otherwise reach near-perfection in diagnostic evaluation trials. A requirement of very high diagnostic performance for clinical adoption, such as a 99% sensitivity, can be rendered nearly unachievable even for a perfect test, if the comparator diagnosis contains even small amounts of uncertainty. This paper and an accompanying online simulation tool demonstrate the effect of classification uncertainty on the apparent performance of tests across a range of typical diagnostic scenarios. Both simulated and real datasets are used to show the degradation of apparent test performance as comparator uncertainty increases.
Overall, a 5% or greater misclassification rate by the comparator can lead to significant underestimation of true test performance. An online simulation tool allows researchers to explore this effect using their own trial parameters (https://imperfect-gold-standard.shinyapps.io/classification-noise/) and the source code is freely available (https://github.com/ksny/Imperfect-Gold-Standard). |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Competing Interests: Leo C. McHugh and Thomas D. Yager declare that they are present or past employees and shareholders of Immunexpress. Leo C. McHugh declares that he is an inventor on the following patents and patent applications filed by Immunexpress: PCT/AU2017/050894 (“Systemic Inflammatory and Pathogen Biomarkers and Uses Therefor”), PCT/AU2016/050927 (“Pathogen Biomarkers and Uses Therefor”), PCT/AU2016/051269 (“Triage Biomarkers and Uses Therefor”), US 15/160,749 (“Validating Biomarker Measurement”), PCT/AU2016/250388 (“Validating Biomarker Measurement”), US Patent 10,167,511 (“Biomarker Identification”), US Patent 10,190,169 (“Biomarker Identification”), US 14/714,188 (“Biomarker signature method, and apparatus and kits therefor”), US 14/616,565 (“Biomarker signature method, and apparatus and kits therefor”), PCT/AU2015/050043 (“Biomarker signature method, and apparatus and kits therefor”). This does not alter our adherence to PLOS ONE policies on sharing data and materials. |
ISSN: | 1932-6203 1932-6203 |
DOI: | 10.1371/journal.pone.0217146 |