Randomized trial on 14 versus 7 days of esomeprazole, moxifloxacin, and amoxicillin for second-line or rescue treatment of Helicobacter pylori infection

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Stephan Miehlke - , Center for Digestive Diseases (Author)
  • Susanne Krasz - , Department of Internal Medicine I (Author)
  • Wulf Schneider-Brachert - , University of Regensburg (Author)
  • Eberhard Kuhlisch - , Institute for Medical Informatics and Biometry (Author)
  • Marco Berning - , Department of Internal Medicine I (Author)
  • Ahmed Madisch - , KRH Hospital Siloah (Author)
  • Martin W. Laass - , Department of Paediatrics (Author)
  • Michael Neumeyer - (Author)
  • Claus Jebens - (Author)
  • Christian Zekorn - (Author)
  • Holger Knoth - , Pharmacy (Author)
  • Michael Vieth - , Klinikum Bayreuth GmbH (Author)
  • Manfred Stolte - , Hospital Kulmbach (Author)
  • Norbert Lehn - , University of Regensburg (Author)
  • Andrea Morgner - , University Hospital Carl Gustav Carus Dresden (Author)

Abstract

Background: Triple therapy with a proton pump inhibitor, moxifloxacin, and amoxicillin has been proven effective in first-line treatment of Helicobacter pylori infection. Aim: To explore 1, the value of triple therapy with esomeprazole, moxifloxacin, and amoxicillin in second-line or rescue treatment of Caucasian patients and 2, the impact of treatment duration on eradication success. Methods: H. pylori-infected patients with at least one previous treatment failure were randomized to oral esomeprazole 20mg b.i.d., moxifloxacin 400mg o.d., and amoxicillin 1000mg b.i.d. for either 7 (EMA-7) or 14days (EMA-14). Eradication was confirmed by 13C urea breath test. Antimicrobial susceptibility testing was performed in all patients at baseline and in patients who failed treatment. Results: Eighty patients were randomized, and 60% had ≥2 previous treatment failures. Pretreatment resistance against clarithromycin and metronidazole was found in 70.5 and 61.5% of cases, respectively. The intention-to-treat eradication rate was significantly higher after EMA-14 compared with EMA-7 (95.0 vs 78.9%, p = .036). No independent risk factor for treatment failure could be identified. There were no serious adverse events. Five of the EMA-14 patients (12.5%) compared with none of the EMA-7 patients discontinued prematurely because of adverse events (p = .031). Post-treatment resistance against moxifloxacin was found in one of seven patients with isolated organisms (14.3%). Conclusion: Second-line/rescue H. pylori eradication therapy with esomeprazole, moxifloxacin, and amoxicillin is very effective and well tolerated. Fourteen days of treatment significantly increase the eradication rate but also the rate of adverse events.

Details

Original languageEnglish
Pages (from-to)420-426
Number of pages7
JournalHelicobacter
Volume16
Issue number6
Publication statusPublished - Dec 2011
Peer-reviewedYes

External IDs

PubMed 22059392

Keywords

Sustainable Development Goals

ASJC Scopus subject areas

Keywords

  • Fluoroquinolone, Helicobacter pylori, Levofloxacin, Moxifloxacin