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10.3164/jcbn.16-49

http://scihub22266oqcxt.onion/10.3164/jcbn.16-49
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C5110942!5110942!27895392
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suck abstract from ncbi


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pmid27895392      J+Clin+Biochem+Nutr 2016 ; 59 (3): 231-7
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  • Determination of the adequate dosage of rebamipide, a gastric mucoprotective drug, to prevent low-dose aspirin-induced gastrointestinal mucosal injury #MMPMID27895392
  • Ota K; Takeuchi T; Nouda S; Ozaki H; Kawaguchi S; Takahashi Y; Harada S; Edogawa S; Kojima Y; Kuramoto T; Higuchi K
  • J Clin Biochem Nutr 2016[Nov]; 59 (3): 231-7 PMID27895392show ga
  • Small intestinal mucosal injury caused by low-dose aspirin is a common cause of obscure gastrointestinal bleeding. We aimed to investigate the protective effects and optimal dose of rebamipide for low-dose aspirin-induced gastrointestinal mucosal injury. In this prospective randomized trial, 45 healthy volunteers (aged 20?65 years) were included and divided into three groups. The groups received enteric-coated aspirin 100 mg (low-dose aspirin) plus omeprazole 10 mg (Group A: proton pump inhibitor group), low-dose aspirin plus rebamipide 300 mg (Group B: standard-dose group), or low-dose aspirin plus rebamipide 900 mg (Group C: high-dose group). Esophagogastroduodenoscopy and video capsule endoscopy were performed, and the fecal occult blood reaction and fecal calprotectin levels were measured before and two weeks after drug administration. Although the fecal calprotectin levels increased significantly in Group A, they did not increase in Groups B and C. The esophagogastroduodenoscopic and video capsule endoscopic findings and the fecal occult blood test findings did not differ significantly among the three groups. In conclusion, standard-dose rebamipide is sufficient for preventing mucosal injury of the small intestine induced by low-dose aspirin, indicating that high-dose rebamipide is not necessary.
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