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A large proportion of fecal immunochemical test-positive participants in colorectal cancer screening is symptomatic
BACKGROUND: Symptomatic invitees are advised not to participate in colorectal cancer (CRC) screening but to directly consult their general practitioner (GP), because fecal immunochemical test (FIT) sensitivity for cancer is not optimal. This recommendation may not always be followed in daily practic...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5949972/ https://www.ncbi.nlm.nih.gov/pubmed/29774162 http://dx.doi.org/10.1177/2050640617733922 |
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author | de Klerk, Clasine M van der Vlugt, Manon Bossuyt, Patrick M Dekker, Evelien |
author_facet | de Klerk, Clasine M van der Vlugt, Manon Bossuyt, Patrick M Dekker, Evelien |
author_sort | de Klerk, Clasine M |
collection | PubMed |
description | BACKGROUND: Symptomatic invitees are advised not to participate in colorectal cancer (CRC) screening but to directly consult their general practitioner (GP), because fecal immunochemical test (FIT) sensitivity for cancer is not optimal. This recommendation may not always be followed in daily practice. We evaluated how many FIT-positive participants had CRC-related symptoms and whether the presence of symptoms was associated with the presence and location of CRC/advanced neoplasia. METHODS: We prospectively collected data on CRC-related symptoms in all FIT-positive participants in the Dutch CRC screening program, referred to our endoscopy centers between 2014 and 2016, and evaluated whether symptoms were associated with detected CRC/advanced neoplasia at colonoscopy. RESULTS: Of 527 FIT-positive participants, 314 had advanced neoplasia, of which 41 had CRC. Overall, 246 (47%; 95% confidence interval (CI) 0.42–0.51) reported CRC-related symptoms. A change in bowel habits (odds ratio (OR) 2.86, CI 1.23–6.62) and visible blood in stool (OR 8.65, CI 2.34–32.0) were associated with the detection of CRC at colonoscopy. We did not observe significant associations between evaluated symptoms and advanced neoplasia. CONCLUSIONS: A large proportion of FIT-positive screening participants have CRC-related symptoms. This suggests that current instructions do not retain symptomatic screening invitees from participation and awareness of CRC-related symptoms is inadequate. |
format | Online Article Text |
id | pubmed-5949972 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-59499722018-05-17 A large proportion of fecal immunochemical test-positive participants in colorectal cancer screening is symptomatic de Klerk, Clasine M van der Vlugt, Manon Bossuyt, Patrick M Dekker, Evelien United European Gastroenterol J Original Articles BACKGROUND: Symptomatic invitees are advised not to participate in colorectal cancer (CRC) screening but to directly consult their general practitioner (GP), because fecal immunochemical test (FIT) sensitivity for cancer is not optimal. This recommendation may not always be followed in daily practice. We evaluated how many FIT-positive participants had CRC-related symptoms and whether the presence of symptoms was associated with the presence and location of CRC/advanced neoplasia. METHODS: We prospectively collected data on CRC-related symptoms in all FIT-positive participants in the Dutch CRC screening program, referred to our endoscopy centers between 2014 and 2016, and evaluated whether symptoms were associated with detected CRC/advanced neoplasia at colonoscopy. RESULTS: Of 527 FIT-positive participants, 314 had advanced neoplasia, of which 41 had CRC. Overall, 246 (47%; 95% confidence interval (CI) 0.42–0.51) reported CRC-related symptoms. A change in bowel habits (odds ratio (OR) 2.86, CI 1.23–6.62) and visible blood in stool (OR 8.65, CI 2.34–32.0) were associated with the detection of CRC at colonoscopy. We did not observe significant associations between evaluated symptoms and advanced neoplasia. CONCLUSIONS: A large proportion of FIT-positive screening participants have CRC-related symptoms. This suggests that current instructions do not retain symptomatic screening invitees from participation and awareness of CRC-related symptoms is inadequate. SAGE Publications 2017-09-24 2018-04 /pmc/articles/PMC5949972/ /pubmed/29774162 http://dx.doi.org/10.1177/2050640617733922 Text en © Author(s) 2017 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial 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). |
spellingShingle | Original Articles de Klerk, Clasine M van der Vlugt, Manon Bossuyt, Patrick M Dekker, Evelien A large proportion of fecal immunochemical test-positive participants in colorectal cancer screening is symptomatic |
title | A large proportion of fecal immunochemical test-positive participants
in colorectal cancer screening is symptomatic |
title_full | A large proportion of fecal immunochemical test-positive participants
in colorectal cancer screening is symptomatic |
title_fullStr | A large proportion of fecal immunochemical test-positive participants
in colorectal cancer screening is symptomatic |
title_full_unstemmed | A large proportion of fecal immunochemical test-positive participants
in colorectal cancer screening is symptomatic |
title_short | A large proportion of fecal immunochemical test-positive participants
in colorectal cancer screening is symptomatic |
title_sort | large proportion of fecal immunochemical test-positive participants
in colorectal cancer screening is symptomatic |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5949972/ https://www.ncbi.nlm.nih.gov/pubmed/29774162 http://dx.doi.org/10.1177/2050640617733922 |
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