PMID- 27460211 OWN - NLM STAT- MEDLINE DCOM- 20170131 LR - 20181202 IS - 1471-230X (Electronic) IS - 1471-230X (Linking) VI - 16 IP - 1 DP - 2016 Jul 26 TI - Pharmacological regimens for eradication of Helicobacter pylori: an overview of systematic reviews and network meta-analysis. PG - 80 LID - 10.1186/s12876-016-0491-7 [doi] LID - 80 AB - BACKGROUND: Approximately half of the world's population is infected with Helicobacter pylori (H.pylori), a bacterium shown to be linked with a series of gastrointestinal diseases. A growing number of systematic reviews (SRs) have been published comparing the effectiveness of different treatments for H.pylori infection but have not reached a consistent conclusion. The objective of this study is to provide an overview of SRs of pharmacological therapies for the eradication of H.pylori. METHODS: Major electronic databases were searched to identify relevant SRs published between 2002 and February 2016. Studies were considered eligible if they included RCTs comparing different pharmacological regimens for treating patients diagnosed as H.pylori infected and pooled the eradication rates in a meta-analysis. A modified version of the 'A Measurement Tool to Assess Systematic Reviews' (AMSTAR) was used to assess the methodological quality. A Bayesian random effects network meta-analysis (NMA) was conducted to compare the different proton pump inhibitors (PPI) within triple therapy. RESULTS: 30 SRs with pairwise meta-analysis were included. In triple therapy, the NMA ranked the esomeprazole to be the most effective PPI, followed by rabeprazole, while no difference was observed among the three old generations of PPI for the eradication of H.pylori. When comparing triple and bismuth-based therapy, the relative effectiveness appeared to be dependent on the choice of antibiotics within the triple therapy; moxifloxacin or levofloxacin-based triple therapy were both associated with greater effectiveness than bismuth-based therapy as a second-line treatment, while bismuth-based therapy achieved similar or greater eradication rate compared to clarithromycin-based therapy. Inconsistent findings were reported regarding the use of levofloxacin/moxifloxacin in the first-line treatment; this could be due to the varied resistant rate to different antibiotics across regions and populations. Critical appraisal showed a low-moderate level of overall methodological quality of included studies. CONCLUSIONS: Our analysis suggests that the new generation of PPIs and use of moxifloxacin or levofloxacin within triple therapy as second-line treatment were associated with greater effectiveness. Given the varied antibiotic resistant rate across regions, the appropriateness of pooling results together in meta-analysis should be carefully considered and the recommendation of the choice of antibiotics should be localized. FAU - Xin, Yiqiao AU - Xin Y AUID- ORCID: 0000-0001-5856-3103 AD - Health Economics and Health Technology Assessment (HEHTA), Institute of Health and Wellbeing, University of Glasgow, Glasgow, UK. yiqiao.xin@glasgow.ac.uk. FAU - Manson, Jan AU - Manson J AD - Knowledge and Information, Healthcare Improvement Scotland, Glasgow, UK. FAU - Govan, Lindsay AU - Govan L AD - Health Economics and Health Technology Assessment (HEHTA), Institute of Health and Wellbeing, University of Glasgow, Glasgow, UK. FAU - Harbour, Robin AU - Harbour R AD - Knowledge and Information, Healthcare Improvement Scotland, Glasgow, UK. FAU - Bennison, Jenny AU - Bennison J AD - Scottish Intercollegiate Guideline Network (SIGN), NHS Education for Scotland, Royal College of General Practitioners (Scotland), Mill Lane Surgery, Edinburgh, UK. FAU - Watson, Eleanor AU - Watson E AD - Department of gastroenterology, Royal Infirmary of Edinburgh, NHS Lothian, Edinburgh, UK. FAU - Wu, Olivia AU - Wu O AD - Health Economics and Health Technology Assessment (HEHTA), Institute of Health and Wellbeing, University of Glasgow, Glasgow, UK. LA - eng PT - Journal Article PT - Meta-Analysis PT - Review PT - Systematic Review DEP - 20160726 PL - England TA - BMC Gastroenterol JT - BMC gastroenterology JID - 100968547 RN - 0 (Antacids) RN - 0 (Anti-Bacterial Agents) RN - 0 (Histamine H2 Antagonists) RN - 0 (Proton Pump Inhibitors) RN - U015TT5I8H (Bismuth) SB - IM MH - Antacids/therapeutic use MH - Anti-Bacterial Agents/*therapeutic use MH - Bismuth/therapeutic use MH - Drug Therapy, Combination MH - Helicobacter Infections/*drug therapy MH - *Helicobacter pylori MH - Histamine H2 Antagonists/therapeutic use MH - Humans MH - Network Meta-Analysis MH - Practice Guidelines as Topic MH - Proton Pump Inhibitors/*therapeutic use PMC - PMC4962503 OTO - NOTNLM OT - Eradication OT - Helicobacter pylori OT - Network meta-analysis OT - Systematic review EDAT- 2016/07/28 06:00 MHDA- 2017/02/01 06:00 PMCR- 2016/07/26 CRDT- 2016/07/28 06:00 PHST- 2015/12/10 00:00 [received] PHST- 2016/07/14 00:00 [accepted] PHST- 2016/07/28 06:00 [entrez] PHST- 2016/07/28 06:00 [pubmed] PHST- 2017/02/01 06:00 [medline] PHST- 2016/07/26 00:00 [pmc-release] AID - 10.1186/s12876-016-0491-7 [pii] AID - 491 [pii] AID - 10.1186/s12876-016-0491-7 [doi] PST - epublish SO - BMC Gastroenterol. 2016 Jul 26;16(1):80. doi: 10.1186/s12876-016-0491-7.