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Small intestinal injury in NSAID users suffering from rheumatoid arthritis or osteoarthritis
Authors:Ilja Tachecí  Petr Bradna  Tomáš Douda  Drahomíra Baštecká  Marcela Kopáčová  Stanislav Rejchrt  Martin Lutonský  Tomáš Soukup  Jan Bureš
Affiliation:1.Second Department of Internal Medicine – Gastroenterology, Faculty of Medicine at Hradec Králové, University Hospital,Charles University in Prague,Hradec Králové,Czech Republic;2.Department of Orthopaedic Surgery, Faculty of Medicine at Hradec Králové, University Hospital,Charles University in Prague,Hradec Králové,Czech Republic
Abstract:
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.
Keywords:
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