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dc.contributor.authorLi, Shuping J.
dc.contributor.authorSharples, Linda D.
dc.contributor.authorBenton, Sally C.
dc.contributor.authorBlyuss, Oleg
dc.contributor.authorMathews, Christopher
dc.contributor.authorSasieni, Peter
dc.contributor.authorDuffy, Stephen W.
dc.date.accessioned2021-01-07T00:09:27Z
dc.date.available2021-01-07T00:09:27Z
dc.date.issued2020-12-20
dc.identifier.citationLi , S J , Sharples , L D , Benton , S C , Blyuss , O , Mathews , C , Sasieni , P & Duffy , S W 2020 , ' Faecal immunochemical testing in bowel cancer screening: Estimating outcomes for different diagnostic policies ' , Journal of Medical Screening . https://doi.org/10.1177/0969141320980501
dc.identifier.issn0969-1413
dc.identifier.otherORCID: /0000-0002-0194-6389/work/86488797
dc.identifier.urihttp://hdl.handle.net/2299/23649
dc.description© 2020 The Author(s). This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
dc.description.abstractObjectives: The National Health Service Bowel Cancer Screening Programme (NHS BCSP) in England has replaced guaiac faecal occult blood testing by faecal immunochemical testing (FIT). There is interest in fully exploiting FIT measures to improve bowel cancer (CRC) screening strategies. In this paper, we estimate the relationship of the quantitative haemoglobin concentration provided by FIT in faecal samples with underlying pathology. From this we estimate thresholds required for given levels of sensitivity to CRC and high-risk adenomas (HRA). Methods: Data were collected from a pilot study of FIT in England in 2014, in which 27,238 participants completed a FIT. Those with a faecal haemoglobin concentration (f-Hb) of at least 20 µg/g were referred for further investigation, usually colonoscopy. Truncated regression models were used to explore the relationship between bowel pathology and FIT results. Regression results were applied to estimate sensitivity to different abnormalities for a number of thresholds. Results: Participants with CRC and HRA had significantly higher f-Hb, and this remained unchanged after adjusting for age and sex. While a threshold of 20 μg/g was estimated to capture 82.2% of CRC and 64.0% of HRA, this would refer 7.8% of participants for colonoscopy. The current programme threshold used in England of 120 μg/g was estimated to identify 47.8% of CRC and 25.0% of HRA. Conclusions: Under the current diagnostic policy of dichotomising FIT results, a very low threshold would be required to achieve high sensitivity to CRC and HRA, which would place further strain on colonoscopy resources. The NHS BCSP in England might benefit from a diagnostic policy that makes greater use of the quantitative nature of FIT.en
dc.format.extent442668
dc.language.isoeng
dc.relation.ispartofJournal of Medical Screening
dc.subjectBowel cancer
dc.subjectcolorectal cancer
dc.subjectfaecal immunochemical test
dc.subjectFIT thresholds
dc.subjectiFOBT
dc.subjectscreening policies
dc.subjectHealth Policy
dc.subjectPublic Health, Environmental and Occupational Health
dc.titleFaecal immunochemical testing in bowel cancer screening: Estimating outcomes for different diagnostic policiesen
dc.contributor.institutionSchool of Physics, Engineering & Computer Science
dc.contributor.institutionDepartment of Physics, Astronomy and Mathematics
dc.description.statusPeer reviewed
dc.identifier.urlhttp://www.scopus.com/inward/record.url?scp=85097845387&partnerID=8YFLogxK
rioxxterms.versionofrecord10.1177/0969141320980501
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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