Efficacy and Safety of Rebamipide in Prevention of NSAID-Gastropathy

Serhiy Tkach, PhD, ScD¹; Liudmila Onischuk²*; Anna Balabantseva³

¹Ukrainian Scientifically Practical Center of Endocrine Surgery, Kyiv, Ukraine, ²Bogomolets National Medical University, Kyiv, Ukraine, ³Medical Academy named after S.I. Georgievsky, Simferopol, Republic of Crimea

*Corresponding author: Lyudmila Onyshchuk, MD. Bogomolets National Medical University, Kyiv, Ukraine. Email: lyudmila.onishhuk@mail.ru

Published: March 17, 2017.  doi: 10.21103/Article7(1)_ShC1

Abstract: 

Background: Nonsteroidal anti-inflammatory drugs (NSAID) are one of the most widely used drugs in medical practice. However, all medical benefits of NSAID are paid for by increased risk of developing numerous side effects. One of the most clinically significant side effects is a NSAID-induced gastrointestinal lesion that develops in, on average, 30% of NSAID users, even with the absence of ulceration; NSAID-induced ulcers and bleeding cause 61% of deaths related to side effects of these medicines. The main aim of this study was to compare the incidence of erosive and ulcerative lesions of the gastroduodenal zone as a result of patients receiving diclofenac on the background of concomitant prophylactic use of proton pump inhibitor (PPI) omeprazole or rebamipide.
Materials and Methods: To achieve this goal we have conducted a randomized comparative study, which included 118 patients aged from 25 to 65 years (mean age, 45±18 years) with osteoarthritis (94 patients) and rheumatoid arthritis (24 patients), who had taken a once-daily dose of 100mg diclofenac (Dikloberl) over 1 month. Depending on the treatment, all patients were randomized into 3 groups by using the computer method of random numbers. Within 1 month, patients of Group 1 (n=42) received additionally a once-daily dose of 20mg omeprazole (Omez), and patients of Group 2 (n=46) - rebamipide at a dose of 100mg three times a day. Patients of Group 3 (n=30) received only diclofenac. The primary endpoint was the cumulative incidence of development of erosions and ulcers in the gastroduodenal zone, which was determined after the treatment according to data from the endoscopy. The secondary endpoint was the incidence of development of dyspeptic symptoms and side effects.
Results: During 1 month of continuous reception of diclofenac, peptic ulcers of stomach and duodenum were found in 2/4.8% and 2/4.8% patients of Group 1 and in 3/6.5% and 2/4.3% patients of Group 2, respectively. In the control group, peptic ulcers of stomach and duodenum were found in 5/16.6% and 3/10% patients, respectively, and in 2 cases, these ulcers (1 gastric ulcer and 1 duodenal ulcer) have manifested into gastrointestinal bleeding. Thus, all peptic ulcers of the gastroduodenal area were detected in 4/9.5% patients of Group 1, 5/10.9% patients of Group 2, and 8/26.6% patients of Group 3.

Keywords: 
NSAID ● side effects ● gastropathy ● rebamipide
References: 
  1. Lassen A, Hallas J, Schaffalitzky de Muckadell OB. Complicated and uncomplicated peptic ulcers in a Danish county 1993–2002: a population-based cohort study. Am J Gastroenterol.  2006;101(5):945–53.
  2. Fujimori S1, Takahashi Y, Gudis K, Seo T, Ehara A, Kobayashi T, et al. Rebamipide has the potential to reduce the intensity of  NSAID-induced small intestinal injury: a double-blind, randomized, controlled trial evaluated by capsule endoscopy. J Gastroenterol. 2011; 46: 57–64. doi: 10.1007/s00535-010-0332-3
  3. Murakami K, Okajima K, Uchiba M, Harada N, Johno M, Okabe H, Takatsuki K. Rebamipide attenuates indomethacin-induced gastric mucosal lesion formation by inhibiting activation of leukocytes in rats. Dig Dis Sci. 1997;42(2):319–25.
  4. Mizukami K, Murakami K, Abe T, Inoue K, Uchida M, Okimoto T, Kodama M, Fujioka T. Aspirin-induced small bowel injuries and the preventive effect of rebamipide. World J Gastroenterol. 2011;17(46):5117–22. doi: 10.3748/wjg.v17.i46.5117.
  5. Dammann HG. Effects of rebamipide on aspirin-induced gastric damage: a case-control study. Eur J Gastroenterol Hepatol. 1994: 6(10):911–6.
  6. Ono S, Kato M, Imai A, Yoshida T, Hirota J, Hata T, et al. Preliminary trial of rebamipide for prevention of low-dose aspirin-induced gastric injury in healthy subjects: a randomized, double-blind, placebo-controlled, cross-over study. J Clin Biochem Nutr. 2009; 45(2):248–53. doi:  10.3164/jcbn.09-24
  7. Kawai T, Takagi Y, Fukuzawa M, Yamagishi T, Goto S. The role of trefoil factor family in apparently healthy subjects administrated gastroprotective agents for the primary prevention of gastrointestinal injuries from low-dose acetylsalicylic acid: a preliminary study. J Clin Biochem Nutr. 2011;49(2):136–40. doi: 10.3164/jcbn.11-10.
  8. Naito Y, Yoshikawa T, Iinuma S, Yagi N, Matsuyama K, Boku Y, et al. Rebamipide protects against indomethacin-induced gastric mucosal injury in healthy volunteers in a double-blind, placebo-controlled study.  Dig Dis Sci. 1998; 43( p Suppl): 83S–89S.
  9. Kim HK, Kim JI, Kim JK, Han JY, Park SH, Choi KY, Chung IS. Preventive effects of rebamipide on NSAID-induced gastric mucosal injury and reduction of gastric mucosal blood flow in healthy volunteers. Dig Dis Sci. 2007;52(8):1776–82.
  10. Naito Y, Iinuma S, Yagi N, Boku Y, Imamoto E, Takagi T, et al. Prevention of Indomethacin-Induced Gastric Mucosal Injury in Helicobacter pylori-Negative Healthy Volunteers: A Comparison Study Rebamipide vs Famotidine.  J Clin Biochem Nutr. 2008:43(1):34–40. doi: 10.3164/jcbn.2008041

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International Journal of Biomedicine. 2017;7(1):57-59. © 2017 International Medical Research and Development Corporation. All rights reserved.