PMID- 28497487 OWN - NLM STAT- MEDLINE DCOM- 20171204 LR - 20220408 IS - 1365-2036 (Electronic) IS - 0269-2813 (Linking) VI - 46 IP - 2 DP - 2017 Jul TI - Systematic review with meta-analysis: the efficacy of vonoprazan-based triple therapy on Helicobacter pylori eradication. PG - 106-114 LID - 10.1111/apt.14130 [doi] AB - BACKGROUND: In order to increase eradication rates, vonoprazan, a novel potassium-competitive acid blocker, has been used in Helicobacter pylori eradication therapy. AIM: To summarise the results of the efficacy of vonoprazan-based triple therapy, helping clinicians to better understand the benefit of vonoprazan in the treatment of H. pylori infection. METHODS: We conducted a systematic literature search on MEDLINE, EMBASE, and the Cochrane Library using the primary keywords "vonoprazan," "takecab", "TAK-438," "potassium," "competitive," "potassium-competitive," "Helicobacter," and "pylori." Studies were included if they evaluated the eradication rate between the vonoprazan-based and proton pump inhibitor (PPI)-based triple therapies. RESULTS: Ten studies and 10 644 patients were evaluated. The crude H. pylori eradication rate determined by intention-to-treat analysis was 87.9% and 72.8% in the vonoprazan-based triple therapy and PPI-based triple therapy respectively. The eradication rate of the vonoprazan-based triple therapy was superior to that of the PPI-based triple therapy (pooled risk ratio [RR] [95% confidence interval (CI)]=1.19 [1.15-1.24]) In addition, there was no significant difference in dropout rate due to adverse event between the regimens (pooled RR of the vonoprazan-based triple therapy [95% CI]=0.69 [0.23-2.03]). The incidence of any adverse events also did not differ between the regimens (pooled RR [95% CI]=1.02 [0.78-1.34]). CONCLUSIONS: The vonoprazan-based triple therapy showed superior efficacy in terms of H. pylori eradication as compared to the PPI-based triple therapy. In addition, the vonoprazan-based triple therapy showed comparable tolerability and incidence of adverse events. CI - (c) 2017 John Wiley & Sons Ltd. FAU - Jung, Y S AU - Jung YS AD - Division of Gastroenterology, Department of Internal Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Korea. FAU - Kim, E H AU - Kim EH AD - Division of Gastroenterology, Department of Internal Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea. FAU - Park, C H AU - Park CH AUID- ORCID: 0000-0003-3824-3481 AD - Department of Internal Medicine, Hanyang University Guri Hospital, Hanyang University College of Medicine, Guri, Korea. LA - eng PT - Journal Article PT - Meta-Analysis PT - Review PT - Systematic Review DEP - 20170512 PL - England TA - Aliment Pharmacol Ther JT - Alimentary pharmacology & therapeutics JID - 8707234 RN - 0 (1-(5-(2-fluorophenyl)-1-(pyridin-3-ylsulfonyl)-1H-pyrrol-3-yl)-N-methylmethanamine) RN - 0 (Anti-Bacterial Agents) RN - 0 (Proton Pump Inhibitors) RN - 0 (Pyrroles) RN - 0 (Sulfonamides) RN - 804826J2HU (Amoxicillin) RN - H1250JIK0A (Clarithromycin) SB - IM CIN - Aliment Pharmacol Ther. 2017 Sep;46(5):551-552. PMID: 28776746 CIN - Aliment Pharmacol Ther. 2017 Sep;46(5):550-551. PMID: 28776748 MH - Amoxicillin/therapeutic use MH - Anti-Bacterial Agents/*therapeutic use MH - Clarithromycin/therapeutic use MH - Drug Therapy, Combination MH - Helicobacter Infections/*drug therapy MH - Helicobacter pylori MH - Humans MH - Proton Pump Inhibitors/*therapeutic use MH - Pyrroles/*therapeutic use MH - Sulfonamides/*therapeutic use EDAT- 2017/05/13 06:00 MHDA- 2017/12/05 06:00 CRDT- 2017/05/13 06:00 PHST- 2017/02/09 00:00 [received] PHST- 2017/03/05 00:00 [revised] PHST- 2017/04/13 00:00 [accepted] PHST- 2017/05/13 06:00 [pubmed] PHST- 2017/12/05 06:00 [medline] PHST- 2017/05/13 06:00 [entrez] AID - 10.1111/apt.14130 [doi] PST - ppublish SO - Aliment Pharmacol Ther. 2017 Jul;46(2):106-114. doi: 10.1111/apt.14130. Epub 2017 May 12.