A prospective evaluation of levofloxacin-based triple therapy for refractory Helicobacter pylori infection in Australia
Autor: | Arun Maseeh, Peter Katelaris, Anthea Katelaris |
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Rok vydání: | 2017 |
Předmět: |
Breath test
medicine.medical_specialty Intention-to-treat analysis medicine.diagnostic_test biology business.industry Rapid urease test Amoxicillin Helicobacter pylori biology.organism_classification Esomeprazole 03 medical and health sciences 0302 clinical medicine Levofloxacin 030220 oncology & carcinogenesis Internal medicine Internal Medicine medicine 030211 gastroenterology & hepatology Adverse effect business medicine.drug |
Zdroj: | Internal Medicine Journal. 47:761-766 |
ISSN: | 1444-0903 |
DOI: | 10.1111/imj.13432 |
Popis: | Background First-line Helicobacter pylori eradication failure is a common and challenging problem. Aim To assess the efficacy of salvage levofloxacin-based triple therapy in Australia. Methods Prospective patients referred after prior treatment failure(s) were prescribed esomeprazole 40 mg, amoxicillin 1 g and levofloxacin 500 mg each twice daily for 10 days. All patients received detailed written and verbal adherence support. Outcome assessment was by 13C-urea breath test and/or histology and urease test. Results In 150 consecutive, evaluable patients (66% female, mean age 54 ± 14 years; six smokers), the main indications for treatment were peptic ulcer disease (17%), increased gastric cancer risk (20%), symptoms (35%) and other risk reduction (28%). The median number of previous treatments was 2 (range 1–7). Eradication of H. pylori was achieved in 90% (intention to treat (ITT)) and 91% (per-protocol (PP)) of patients. The eradication rate did not differ according to the type or number of prior treatments: 93% when ≤2 (n = 107) compared with 84% after three or more prior treatments (n = 43; P = 0.13) or with age, ethnicity or indication for treatment but it was higher in females (ITT 94 vs 82%, P = 0.04). Adherence was excellent (95%). No serious adverse effects were observed; mild adverse effects were reported in 11%. No primary levofloxacin resistance was observed in 20 concurrent cases. Conclusion The efficacy and safety of this levofloxacin-based triple therapy suggests it should be used as a salvage regimen in this region. Randomised comparative trials are unlikely to be done but these data compare favourably with local data for other salvage therapies. |
Databáze: | OpenAIRE |
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