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Value of routine duodenal mucosal biopsies in the evaluation of anemia in a large Australian referral centre

BACKGROUND AND AIM: Small bowel mucosal biopsies (SBBx) are routinely performed to investigate unexplained anemia; however, previous studies have demonstrated a low yield in diagnosing celiac disease. Our aim was to determine the yield of routine SBBx in a large cohort of patients who underwent gast...

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Autores principales: Young, Edward, Ooi, Marie, Nguyen, Nam Q
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Publishing Asia Pty Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6206981/
https://www.ncbi.nlm.nih.gov/pubmed/30483588
http://dx.doi.org/10.1002/jgh3.12064
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author Young, Edward
Ooi, Marie
Nguyen, Nam Q
author_facet Young, Edward
Ooi, Marie
Nguyen, Nam Q
author_sort Young, Edward
collection PubMed
description BACKGROUND AND AIM: Small bowel mucosal biopsies (SBBx) are routinely performed to investigate unexplained anemia; however, previous studies have demonstrated a low yield in diagnosing celiac disease. Our aim was to determine the yield of routine SBBx in a large cohort of patients who underwent gastroscopy for the investigation of anemia. METHODS: Data from consecutive patients who underwent gastroscopy for the investigation of anemia in a tertiary hospital, from January 2008–December 2011, were prospectively collected. Measured outcomes were the prevalence of celiac disease, the yield of duodenal biopsies, and the correlation between celiac serology and diagnosis. RESULTS: Over 4 years, 987 patients (385 M:602 F; 48.27 ± 15.89 years) underwent endoscopy for anemia, of which 534 (54.1%) had proven iron deficiency anemia (IDA). Abnormal SBBx consistent with celiac disease were found in 2% (22/987), with a higher prevalence in females (3.2%, n = 19 vs 0.8%, n = 3 in males) and in those with IDA (3.6%, n = 19 vs 0.7%, n = 3 in non‐IDA). Macroscopic endoscopic abnormalities were present in 86% (19/22) of patients with celiac disease. Of the 178 patients who had celiac serology, tissue transglutaminase antibody had the highest sensitivity (80%) and specificity (99%). Combined serology had a sensitivity of 85.7%. CONCLUSION: Only 2% of patients with unexplained anemia had abnormal SBBx consistent with celiac disease and even fewer patients in non‐IDA. Given the availability and high sensitivity of celiac serology and macroscopic changes on endoscopy, SBBx should not be routine during endoscopy but should be limited to those with positive celiac serology, abnormal endoscopic appearance, or females with IDA.
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spelling pubmed-62069812018-11-27 Value of routine duodenal mucosal biopsies in the evaluation of anemia in a large Australian referral centre Young, Edward Ooi, Marie Nguyen, Nam Q JGH Open Original Articles BACKGROUND AND AIM: Small bowel mucosal biopsies (SBBx) are routinely performed to investigate unexplained anemia; however, previous studies have demonstrated a low yield in diagnosing celiac disease. Our aim was to determine the yield of routine SBBx in a large cohort of patients who underwent gastroscopy for the investigation of anemia. METHODS: Data from consecutive patients who underwent gastroscopy for the investigation of anemia in a tertiary hospital, from January 2008–December 2011, were prospectively collected. Measured outcomes were the prevalence of celiac disease, the yield of duodenal biopsies, and the correlation between celiac serology and diagnosis. RESULTS: Over 4 years, 987 patients (385 M:602 F; 48.27 ± 15.89 years) underwent endoscopy for anemia, of which 534 (54.1%) had proven iron deficiency anemia (IDA). Abnormal SBBx consistent with celiac disease were found in 2% (22/987), with a higher prevalence in females (3.2%, n = 19 vs 0.8%, n = 3 in males) and in those with IDA (3.6%, n = 19 vs 0.7%, n = 3 in non‐IDA). Macroscopic endoscopic abnormalities were present in 86% (19/22) of patients with celiac disease. Of the 178 patients who had celiac serology, tissue transglutaminase antibody had the highest sensitivity (80%) and specificity (99%). Combined serology had a sensitivity of 85.7%. CONCLUSION: Only 2% of patients with unexplained anemia had abnormal SBBx consistent with celiac disease and even fewer patients in non‐IDA. Given the availability and high sensitivity of celiac serology and macroscopic changes on endoscopy, SBBx should not be routine during endoscopy but should be limited to those with positive celiac serology, abnormal endoscopic appearance, or females with IDA. Wiley Publishing Asia Pty Ltd 2018-07-05 /pmc/articles/PMC6206981/ /pubmed/30483588 http://dx.doi.org/10.1002/jgh3.12064 Text en © 2018 The Authors. JGH Open: An open access journal of gastroenterology and hepatology published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Young, Edward
Ooi, Marie
Nguyen, Nam Q
Value of routine duodenal mucosal biopsies in the evaluation of anemia in a large Australian referral centre
title Value of routine duodenal mucosal biopsies in the evaluation of anemia in a large Australian referral centre
title_full Value of routine duodenal mucosal biopsies in the evaluation of anemia in a large Australian referral centre
title_fullStr Value of routine duodenal mucosal biopsies in the evaluation of anemia in a large Australian referral centre
title_full_unstemmed Value of routine duodenal mucosal biopsies in the evaluation of anemia in a large Australian referral centre
title_short Value of routine duodenal mucosal biopsies in the evaluation of anemia in a large Australian referral centre
title_sort value of routine duodenal mucosal biopsies in the evaluation of anemia in a large australian referral centre
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6206981/
https://www.ncbi.nlm.nih.gov/pubmed/30483588
http://dx.doi.org/10.1002/jgh3.12064
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