Prevention of gastric mucosal injury induced by anti-platelet drugs by famotidine

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Abstract

Anti-platelet drug-induced gastric mucosal injury correlates with intragastric pH. Our aim was to investigate prophylaxis effects of famotidine, one of the representative histamine-2 receptor antagonists (H2RA), on gastric mucosal injury induced by dual therapy with low-dose aspirin and clopidogrel in relation to Helicobacter pylori (H. pylori) infection and CYP2C19 genotypes. This study was conducted for 20 healthy Japanese volunteers (10 H. pylori-positive and 10-negative subjects) with 100mg aspirin plus 75mg clopidogrel (AC) once-daily dosing and AC plus 20mg famotidine twice-daily dosing (ACH). Mucosal injury was endoscopically assessed on day 3 and 7 and 24-hour intragastric pH and antiplatelet-function test was performed on day 7. Median pH in ACH was similar between CYP2C19 extensive metabolizer (EM) and intermediate metabolizer (IM)/poor metabolizer (PM) and was significantly higher in H. pylori-positive than negative subjects (P

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Uotani, T., Sugimoto, M., Nishino, M., Ichikawa, H., Sahara, S., Yamade, M., … Furuta, T. (2014). Prevention of gastric mucosal injury induced by anti-platelet drugs by famotidine. Journal of Clinical Pharmacology, 54(8), 858–864. https://doi.org/10.1002/jcph.284

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