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Evaluation of a fecal immunochemistry test prior to colonoscopy for outpatients with various indications

BACKGROUND: Stool tests can predict advanced neoplasms prior to colonoscopy. Results of immunochemical stool tests to predict findings at colonoscopy for various indications are less often reported. We compared pre-colonoscopy stool tests with findings in patients undergoing colonoscopy for differen...

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Autores principales: Szilagyi, Andrew, Xue, Xiaoqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5689031/
https://www.ncbi.nlm.nih.gov/pubmed/29184430
http://dx.doi.org/10.2147/CEG.S147928
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author Szilagyi, Andrew
Xue, Xiaoqing
author_facet Szilagyi, Andrew
Xue, Xiaoqing
author_sort Szilagyi, Andrew
collection PubMed
description BACKGROUND: Stool tests can predict advanced neoplasms prior to colonoscopy. Results of immunochemical stool tests to predict findings at colonoscopy for various indications are less often reported. We compared pre-colonoscopy stool tests with findings in patients undergoing colonoscopy for different indications. PATIENTS AND METHODS: Charts of patients undergoing elective or semi-urgent colonoscopy were reviewed. Comparison of adenoma detection rates and pathological findings was made between prescreened and non-prescreened, and between stool-positive and stool-negative cases. Demographics, quality of colonoscopy, and pathological findings were recorded. Odds ratios (ORs) and 95% confidence intervals (CIs) were assessed. Statistical significance was accepted at p≤0.05. RESULTS: Charts of 325 patients were reviewed. Among them, stool tests were done on 144 patients: 114 were negative and 30 were positive. Findings were similar in the pretest and non-pretest groups. Detection of advanced adenomas per patient was higher in the stool-positive group compared to the stool-negative group (23.4% vs 3.5%, p=0.0016, OR =7.6 [95% CI: 2–29.3]). Five advanced adenomas (without high-grade dysplasia or adenocarcinoma) and several cases of multiple adenomas were missed in the negative group. Sensitivity and specificity for advanced polyps was 63.6% and 82.7%, respectively. The negative predictive value was 96.5%. Male gender was independently predictive of any adenoma. CONCLUSION: The stool immunochemical test best predicted advanced neoplasms and had a high negative predictive value in this small cohort. Whether this test can be applied to determine the need for colonoscopy in groups other than average risk would require more studies.
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spelling pubmed-56890312017-11-28 Evaluation of a fecal immunochemistry test prior to colonoscopy for outpatients with various indications Szilagyi, Andrew Xue, Xiaoqing Clin Exp Gastroenterol Original Research BACKGROUND: Stool tests can predict advanced neoplasms prior to colonoscopy. Results of immunochemical stool tests to predict findings at colonoscopy for various indications are less often reported. We compared pre-colonoscopy stool tests with findings in patients undergoing colonoscopy for different indications. PATIENTS AND METHODS: Charts of patients undergoing elective or semi-urgent colonoscopy were reviewed. Comparison of adenoma detection rates and pathological findings was made between prescreened and non-prescreened, and between stool-positive and stool-negative cases. Demographics, quality of colonoscopy, and pathological findings were recorded. Odds ratios (ORs) and 95% confidence intervals (CIs) were assessed. Statistical significance was accepted at p≤0.05. RESULTS: Charts of 325 patients were reviewed. Among them, stool tests were done on 144 patients: 114 were negative and 30 were positive. Findings were similar in the pretest and non-pretest groups. Detection of advanced adenomas per patient was higher in the stool-positive group compared to the stool-negative group (23.4% vs 3.5%, p=0.0016, OR =7.6 [95% CI: 2–29.3]). Five advanced adenomas (without high-grade dysplasia or adenocarcinoma) and several cases of multiple adenomas were missed in the negative group. Sensitivity and specificity for advanced polyps was 63.6% and 82.7%, respectively. The negative predictive value was 96.5%. Male gender was independently predictive of any adenoma. CONCLUSION: The stool immunochemical test best predicted advanced neoplasms and had a high negative predictive value in this small cohort. Whether this test can be applied to determine the need for colonoscopy in groups other than average risk would require more studies. Dove Medical Press 2017-11-10 /pmc/articles/PMC5689031/ /pubmed/29184430 http://dx.doi.org/10.2147/CEG.S147928 Text en © 2017 Szilagyi and Xue. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Szilagyi, Andrew
Xue, Xiaoqing
Evaluation of a fecal immunochemistry test prior to colonoscopy for outpatients with various indications
title Evaluation of a fecal immunochemistry test prior to colonoscopy for outpatients with various indications
title_full Evaluation of a fecal immunochemistry test prior to colonoscopy for outpatients with various indications
title_fullStr Evaluation of a fecal immunochemistry test prior to colonoscopy for outpatients with various indications
title_full_unstemmed Evaluation of a fecal immunochemistry test prior to colonoscopy for outpatients with various indications
title_short Evaluation of a fecal immunochemistry test prior to colonoscopy for outpatients with various indications
title_sort evaluation of a fecal immunochemistry test prior to colonoscopy for outpatients with various indications
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5689031/
https://www.ncbi.nlm.nih.gov/pubmed/29184430
http://dx.doi.org/10.2147/CEG.S147928
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