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   <subfield code="a">10.1007/s00535-010-0332-3</subfield>
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   <subfield code="a">Rebamipide has the potential to reduce the intensity of NSAID-induced small intestinal injury: a double-blind, randomized, controlled trial evaluated by capsule endoscopy</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Shunji Fujimori, Yoko Takahashi, Katya Gudis, Tsuguhiko Seo, Akihito Ehara, Tsuyoshi Kobayashi, Keigo Mitsui, Masaoki Yonezawa, Shu Tanaka, Atsushi Tatsuguchi, Choitsu Sakamoto]</subfield>
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   <subfield code="a">Background: A study reported that rebamipide was effective at reducing short-term nonsteroidal anti-inflammatory drug (NSAID)-induced enteropathy. The purpose of this study was to re-evaluate the effect of the co-administration of rebamipide on small intestinal injuries induced by short-term NSAID treatment. Methods: Eighty healthy male volunteers were randomly assigned to two study groups: a control group (N=40), which received NSAID (diclofenac sodium, 75mg/day) and omeprazole (20mg/day) treatment along with a placebo; and a rebamipide group, which received NSAID, omeprazole and rebamipide (300mg/day). Small intestinal injuries (mucosal breaks plus denuded areas) were evaluated by capsule endoscopy before and after 14days of treatment. Results: A total of 38 control subjects and 34 rebamipide subjects completed the treatment and were evaluated by capsule endoscopy. NSAID therapy increased the mean number of mucosal injuries per subject from a basal level of 0.1±0.3 to 16±71 and 4.2±7.8 in the control and rebamipide groups, respectively, but the difference was not significant. The difference in the percentage of subjects with at least one mucosal injury post-treatment was also not significant (control 63%; rebamipide 47%). Limiting our analysis to subjects with mucosal injuries, rebamipide co-treatment had the tendency to reduce the mean number of mucosal injuries per subject from 25 in the control group to 8.9 in the rebamipide group (multiple comparisons test; p=0.088, Mann-Whitney U test; p=0.038). Conclusions: Rebamipide co-therapy had the potential to reduce the intensity of small intestinal injury induced by 2-week administration of diclofenac.</subfield>
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   <subfield code="a">Springer, 2010</subfield>
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   <subfield code="a">Small intestinal injury</subfield>
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   <subfield code="a">NSAID</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Rebamipide</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Prevention</subfield>
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   <subfield code="a">Capsule endoscopy</subfield>
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   <subfield code="a">Fujimori</subfield>
   <subfield code="D">Shunji</subfield>
   <subfield code="u">Division of Gastroenterology, Department of Internal Medicine, Nippon Medical School, 1-1-5 Sendagi, Bunkyo-ku, 113-8603, Tokyo, Japan</subfield>
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   <subfield code="a">Takahashi</subfield>
   <subfield code="D">Yoko</subfield>
   <subfield code="u">Division of Gastroenterology, Department of Internal Medicine, Nippon Medical School, 1-1-5 Sendagi, Bunkyo-ku, 113-8603, Tokyo, Japan</subfield>
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   <subfield code="a">Gudis</subfield>
   <subfield code="D">Katya</subfield>
   <subfield code="u">Division of Gastroenterology, Department of Internal Medicine, Nippon Medical School, 1-1-5 Sendagi, Bunkyo-ku, 113-8603, Tokyo, Japan</subfield>
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   <subfield code="a">Seo</subfield>
   <subfield code="D">Tsuguhiko</subfield>
   <subfield code="u">Division of Gastroenterology, Department of Internal Medicine, Nippon Medical School, 1-1-5 Sendagi, Bunkyo-ku, 113-8603, Tokyo, Japan</subfield>
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   <subfield code="a">Ehara</subfield>
   <subfield code="D">Akihito</subfield>
   <subfield code="u">Division of Gastroenterology, Department of Internal Medicine, Nippon Medical School, 1-1-5 Sendagi, Bunkyo-ku, 113-8603, Tokyo, Japan</subfield>
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   <subfield code="a">Kobayashi</subfield>
   <subfield code="D">Tsuyoshi</subfield>
   <subfield code="u">Division of Gastroenterology, Department of Internal Medicine, Nippon Medical School, 1-1-5 Sendagi, Bunkyo-ku, 113-8603, Tokyo, Japan</subfield>
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   <subfield code="a">Mitsui</subfield>
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   <subfield code="u">Division of Gastroenterology, Department of Internal Medicine, Nippon Medical School, 1-1-5 Sendagi, Bunkyo-ku, 113-8603, Tokyo, Japan</subfield>
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   <subfield code="a">Yonezawa</subfield>
   <subfield code="D">Masaoki</subfield>
   <subfield code="u">Division of Gastroenterology, Department of Internal Medicine, Nippon Medical School, 1-1-5 Sendagi, Bunkyo-ku, 113-8603, Tokyo, Japan</subfield>
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   <subfield code="a">Tanaka</subfield>
   <subfield code="D">Shu</subfield>
   <subfield code="u">Division of Gastroenterology, Department of Internal Medicine, Nippon Medical School, 1-1-5 Sendagi, Bunkyo-ku, 113-8603, Tokyo, Japan</subfield>
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   <subfield code="a">Tatsuguchi</subfield>
   <subfield code="D">Atsushi</subfield>
   <subfield code="u">Division of Gastroenterology, Department of Internal Medicine, Nippon Medical School, 1-1-5 Sendagi, Bunkyo-ku, 113-8603, Tokyo, Japan</subfield>
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   <subfield code="a">Sakamoto</subfield>
   <subfield code="D">Choitsu</subfield>
   <subfield code="u">Division of Gastroenterology, Department of Internal Medicine, Nippon Medical School, 1-1-5 Sendagi, Bunkyo-ku, 113-8603, Tokyo, Japan</subfield>
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   <subfield code="t">Journal of Gastroenterology</subfield>
   <subfield code="d">Springer Japan</subfield>
   <subfield code="g">46/1(2011-01-01), 57-64</subfield>
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   <subfield code="q">46:1&lt;57</subfield>
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