Literature DB >> 28559221

Amoxycillin and Metronidazole Therapy for Helicobacter pylori Eradication: A 10-Year Trend in Turin, Italy.

Davide Giuseppe Ribaldone1, Marco Astegiano1, Giorgio Saracco2, Rinaldo Pellicano1.   

Abstract

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Year:  2017        PMID: 28559221      PMCID: PMC5450874          DOI: 10.4274/balkanmedj.2015.1714

Source DB:  PubMed          Journal:  Balkan Med J        ISSN: 2146-3123            Impact factor:   2.021


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To The Editor,

Helicobacter pylori (H. pylori) infection plays a crucial role in causing gastritis and peptic ulcer disease (PUD). To date, despite the several regimens proposed, no therapy leads to a 100% H. pylori eradication rate (1). As the antimicrobial activity of metronidazole is marginally affected by low pH, this drug may be highly effective against H. pylori. The European Helicobacter Study Group has advised to employ a metronidazole-based triple therapy as choice in treating H. pylori infection in relation to specific resistance rate in each region (2). Recently, a multicentric study revealed that, in Southern Europe, the primary rate of H. pylori metronidazole resistance was around 30% (3). In 2002, we found that in Turin, Northern Italy, a triple therapy with metronidazole, amoxycillin and a proton pump inhibitor (PPI) for 7 days or for 10 days, achieved an eradication rate of 73.5% or 71.6%, respectively. Lengthening the treatment conferred no advantages. These values were significantly lower compared to those reported earlier (4). In a subsequent study with alternative schedules (cefixime plus metronidazole), the results did not improve (5). As antibiotic resistance is an evolving process, it is mandatory to carry out surveys in order to be guided in the therapeutic choice. Hence, in the year 2013 (January 01 - December 31), we evaluated prospectively the H. pylori eradication rate of consecutive naive patients, treated with a triple therapy comprising a standard dose of PPI, amoxycillin 1 g and metronidazole 500 mg twice daily. Results were compared with a previous randomized prospective study conducted 10 years earlier with the same schedule (4). Eradication of H. pylori infection was assessed by 13C-urea breath test, performed according to the supplier’s instructions (Helicobacter Test, INFAI®, Bochum, Germany). The reported sensitivity is 97.9% and specificity 98.5%. Samples were analysed for 13C/12C ratio with a mass spectrometer (BreathMAT plus, Finnigan, Bremen, Germany). Results were expressed as excess ð13CO2 excretion per mil: a value >4 delta per mil was considered positive. No patient had received PPI or antibiotics in the last 30 days. All patients gave their written informed consent. Differences in eradication rates were tested with the chi-square test (with Yates’ correction for continuity). A p value <0.05 was considered significant. The cohort included 66 patients (40 males, mean age 61.6, range 39-62), 39 of them received a regimen including a 1-week triple therapy (group I) and 27 were treated with a 10-day triple therapy (group II). Forty-two of them had a previous diagnosis of PUD or gastroduodenal erosions, and the remaining of active gastritis. The overall H. pylori eradication rate was 69.2% (27/39) in group I and 70% (19/27) in group II, without significant difference (p=0.96). When compared with the prospective study published in the year 2002 (4) no differences were observed in the effectiveness of therapy (p=0.81 for 7 days and p=0.95 for 10 days) (Table 1). In conclusion, in our area, a metronidazole-based treatment regimen for H. pylori eradication, although unsatisfactory, is as effective as 10 years ago.
Table 1

Results of H. pylori eradication regimens

  5 in total

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3.  Preparation and In Vitro-In Vivo Evaluation of Luteolin Loaded Gastroretentive Microsponge for the Eradication of Helicobacter pylori Infections.

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  3 in total

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