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Diagnostic accuracy of fecal calprotectin in predicting significant gastrointestinal diseases
BACKGROUND AND AIM: It is often unreliable to triage patients for timely endoscopic investigations based on symptoms alone. We need an objective assessment to differentiate between organic gastrointestinal diseases and functional bowel symptoms. We evaluated the diagnostic accuracy of fecal calprote...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wiley Publishing Asia Pty Ltd
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8171161/ https://www.ncbi.nlm.nih.gov/pubmed/34124380 http://dx.doi.org/10.1002/jgh3.12548 |
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author | Kan, Yee Man Chu, Sin Yan Loo, Ching Kong |
author_facet | Kan, Yee Man Chu, Sin Yan Loo, Ching Kong |
author_sort | Kan, Yee Man |
collection | PubMed |
description | BACKGROUND AND AIM: It is often unreliable to triage patients for timely endoscopic investigations based on symptoms alone. We need an objective assessment to differentiate between organic gastrointestinal diseases and functional bowel symptoms. We evaluated the diagnostic accuracy of fecal calprotectin (FC) in predicting organic gastrointestinal diseases. METHODS: In a prospective observational study, consecutive patients referred for colonoscopy to the Department of Medicine and Geriatrics at the Kwong Wah Hospital in Hong Kong were recruited. Stool samples were collected within 24 h before colonoscopy. FC was measured by a commercial kit. Upper endoscopy investigations were then proceeded if normal colonoscopy but elevated FC. RESULTS: Two hundred and seventy out of 429 patients had FC above 50 μg/g. Eighty‐six out of 270 with elevated FC had significant colonoscopy pathological findings. The sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) of FC test for diagnosing a significant organic colonoscopy or upper endoscopy disease were 91.7, 55.6, 57.0, and 91.2%, respectively. The NPV of FC for colorectal cancer, high risk polyp, and colon inflammation were 98.7, 96.2, and 98.1%, respectively. The NPV of FC in the condition of altered bowel habit or abdominal pain in predicting colorectal cancer and inflammation were 93.8 and 100%, respectively. CONCLUSIONS: FC is a reliable marker of ruling out organic bowel diseases. A single negative FC test could be used as a triage tool to prioritize the need and urgency of further investigation, particularly in the setting of altered bowel habits and abdominal pain. |
format | Online Article Text |
id | pubmed-8171161 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Wiley Publishing Asia Pty Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-81711612021-06-11 Diagnostic accuracy of fecal calprotectin in predicting significant gastrointestinal diseases Kan, Yee Man Chu, Sin Yan Loo, Ching Kong JGH Open Original Articles BACKGROUND AND AIM: It is often unreliable to triage patients for timely endoscopic investigations based on symptoms alone. We need an objective assessment to differentiate between organic gastrointestinal diseases and functional bowel symptoms. We evaluated the diagnostic accuracy of fecal calprotectin (FC) in predicting organic gastrointestinal diseases. METHODS: In a prospective observational study, consecutive patients referred for colonoscopy to the Department of Medicine and Geriatrics at the Kwong Wah Hospital in Hong Kong were recruited. Stool samples were collected within 24 h before colonoscopy. FC was measured by a commercial kit. Upper endoscopy investigations were then proceeded if normal colonoscopy but elevated FC. RESULTS: Two hundred and seventy out of 429 patients had FC above 50 μg/g. Eighty‐six out of 270 with elevated FC had significant colonoscopy pathological findings. The sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) of FC test for diagnosing a significant organic colonoscopy or upper endoscopy disease were 91.7, 55.6, 57.0, and 91.2%, respectively. The NPV of FC for colorectal cancer, high risk polyp, and colon inflammation were 98.7, 96.2, and 98.1%, respectively. The NPV of FC in the condition of altered bowel habit or abdominal pain in predicting colorectal cancer and inflammation were 93.8 and 100%, respectively. CONCLUSIONS: FC is a reliable marker of ruling out organic bowel diseases. A single negative FC test could be used as a triage tool to prioritize the need and urgency of further investigation, particularly in the setting of altered bowel habits and abdominal pain. Wiley Publishing Asia Pty Ltd 2021-05-06 /pmc/articles/PMC8171161/ /pubmed/34124380 http://dx.doi.org/10.1002/jgh3.12548 Text en © 2021 The Authors. JGH Open published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Kan, Yee Man Chu, Sin Yan Loo, Ching Kong Diagnostic accuracy of fecal calprotectin in predicting significant gastrointestinal diseases |
title | Diagnostic accuracy of fecal calprotectin in predicting significant gastrointestinal diseases |
title_full | Diagnostic accuracy of fecal calprotectin in predicting significant gastrointestinal diseases |
title_fullStr | Diagnostic accuracy of fecal calprotectin in predicting significant gastrointestinal diseases |
title_full_unstemmed | Diagnostic accuracy of fecal calprotectin in predicting significant gastrointestinal diseases |
title_short | Diagnostic accuracy of fecal calprotectin in predicting significant gastrointestinal diseases |
title_sort | diagnostic accuracy of fecal calprotectin in predicting significant gastrointestinal diseases |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8171161/ https://www.ncbi.nlm.nih.gov/pubmed/34124380 http://dx.doi.org/10.1002/jgh3.12548 |
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