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...
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Published in | Rheumatology international Vol. 36; no. 11; pp. 1557 - 1561 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer Berlin Heidelberg
01.11.2016
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | 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. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 0172-8172 1437-160X 1437-160X |
DOI: | 10.1007/s00296-016-3552-x |