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Small intestinal injury in NSAID users suffering from rheumatoid arthritis or osteoarthritis
The goal of this prospective study was to assess non-steroidal anti-inflammatory drug (NSAID)-induced enteropathy in patients with rheumatoid arthritis (RA) or osteoarthritis (OA) by means of non-invasive wireless capsule enteroscopy. A total of 143 patients (74 with RA, 69 with OA) treated with NSA...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5055563/ https://www.ncbi.nlm.nih.gov/pubmed/27549792 http://dx.doi.org/10.1007/s00296-016-3552-x |
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author | Tachecí, Ilja Bradna, Petr Douda, Tomáš Baštecká, Drahomíra Kopáčová, Marcela Rejchrt, Stanislav Lutonský, Martin Soukup, Tomáš Bureš, Jan |
author_facet | Tachecí, Ilja Bradna, Petr Douda, Tomáš Baštecká, Drahomíra Kopáčová, Marcela Rejchrt, Stanislav Lutonský, Martin Soukup, Tomáš Bureš, Jan |
author_sort | Tachecí, Ilja |
collection | PubMed |
description | The goal of this prospective study was to assess non-steroidal anti-inflammatory drug (NSAID)-induced enteropathy in patients with rheumatoid arthritis (RA) or osteoarthritis (OA) by means of non-invasive wireless capsule enteroscopy. A total of 143 patients (74 with RA, 69 with OA) treated with NSAIDs (>1 month) and 42 healthy volunteers were included. All subjects underwent capsule endoscopy, laboratory tests and filled in questionnaires. The severity of small bowel injury was graded as: mild (red spots or sporadic erosions), moderate (10–20 erosions) or severe (>20 erosions or ulcers). Capsule endoscopy identified small bowel lesions in 44.8 % of patients (mild 36.4 %, moderate 3.5 % and severe in 4.9 %). Mild non-specific lesions were found in 11.9 % healthy volunteers. There was a significantly higher prevalence of enteropathy in RA (56.8 %) compared to OA (31.9 %, p < 0.01). A significant difference between NSAID users (RA and OA) with and without enteropathy was observed in erythrocytes (p < 0.01), the leucocyte count (p < 0.05), haemoglobin (p < 0.05), haematocrit (p < 0.05), serum albumin (p < 0.01) and erythrocyte sedimentation rate (p < 0.05). No relationship was found between enteropathy and dyspepsia, gender or age. NSAID therapy is associated with a significant risk of small bowel injury. The risk is significantly higher in RA patients suggesting a possible influence of the underlying disease. Trial registration number: DRKS00004940. |
format | Online Article Text |
id | pubmed-5055563 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-50555632016-10-26 Small intestinal injury in NSAID users suffering from rheumatoid arthritis or osteoarthritis Tachecí, Ilja Bradna, Petr Douda, Tomáš Baštecká, Drahomíra Kopáčová, Marcela Rejchrt, Stanislav Lutonský, Martin Soukup, Tomáš Bureš, Jan Rheumatol Int Safety and Pharmacovigillance The goal of this prospective study was to assess non-steroidal anti-inflammatory drug (NSAID)-induced enteropathy in patients with rheumatoid arthritis (RA) or osteoarthritis (OA) by means of non-invasive wireless capsule enteroscopy. A total of 143 patients (74 with RA, 69 with OA) treated with NSAIDs (>1 month) and 42 healthy volunteers were included. All subjects underwent capsule endoscopy, laboratory tests and filled in questionnaires. The severity of small bowel injury was graded as: mild (red spots or sporadic erosions), moderate (10–20 erosions) or severe (>20 erosions or ulcers). Capsule endoscopy identified small bowel lesions in 44.8 % of patients (mild 36.4 %, moderate 3.5 % and severe in 4.9 %). Mild non-specific lesions were found in 11.9 % healthy volunteers. There was a significantly higher prevalence of enteropathy in RA (56.8 %) compared to OA (31.9 %, p < 0.01). A significant difference between NSAID users (RA and OA) with and without enteropathy was observed in erythrocytes (p < 0.01), the leucocyte count (p < 0.05), haemoglobin (p < 0.05), haematocrit (p < 0.05), serum albumin (p < 0.01) and erythrocyte sedimentation rate (p < 0.05). No relationship was found between enteropathy and dyspepsia, gender or age. NSAID therapy is associated with a significant risk of small bowel injury. The risk is significantly higher in RA patients suggesting a possible influence of the underlying disease. Trial registration number: DRKS00004940. Springer Berlin Heidelberg 2016-08-22 2016 /pmc/articles/PMC5055563/ /pubmed/27549792 http://dx.doi.org/10.1007/s00296-016-3552-x Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Safety and Pharmacovigillance Tachecí, Ilja Bradna, Petr Douda, Tomáš Baštecká, Drahomíra Kopáčová, Marcela Rejchrt, Stanislav Lutonský, Martin Soukup, Tomáš Bureš, Jan Small intestinal injury in NSAID users suffering from rheumatoid arthritis or osteoarthritis |
title | Small intestinal injury in NSAID users suffering from rheumatoid arthritis or osteoarthritis |
title_full | Small intestinal injury in NSAID users suffering from rheumatoid arthritis or osteoarthritis |
title_fullStr | Small intestinal injury in NSAID users suffering from rheumatoid arthritis or osteoarthritis |
title_full_unstemmed | Small intestinal injury in NSAID users suffering from rheumatoid arthritis or osteoarthritis |
title_short | Small intestinal injury in NSAID users suffering from rheumatoid arthritis or osteoarthritis |
title_sort | small intestinal injury in nsaid users suffering from rheumatoid arthritis or osteoarthritis |
topic | Safety and Pharmacovigillance |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5055563/ https://www.ncbi.nlm.nih.gov/pubmed/27549792 http://dx.doi.org/10.1007/s00296-016-3552-x |
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