Rifabutin-based 'rescue therapy' for Helicobacter pylori infected patients after failure of standard regimens
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Perri, F
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IRCCS, Casa Sollievo Sofferenza Hosp, Div Gastroenterol, I-71013 San Giovanni Rotondo, ItalyIRCCS, Casa Sollievo Sofferenza Hosp, Div Gastroenterol, I-71013 San Giovanni Rotondo, Italy
Perri, F
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Festa, V
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IRCCS, Casa Sollievo Sofferenza Hosp, Div Gastroenterol, I-71013 San Giovanni Rotondo, ItalyIRCCS, Casa Sollievo Sofferenza Hosp, Div Gastroenterol, I-71013 San Giovanni Rotondo, Italy
Festa, V
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]
Clemente, R
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IRCCS, Casa Sollievo Sofferenza Hosp, Div Gastroenterol, I-71013 San Giovanni Rotondo, ItalyIRCCS, Casa Sollievo Sofferenza Hosp, Div Gastroenterol, I-71013 San Giovanni Rotondo, Italy
Clemente, R
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Quitadamo, M
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IRCCS, Casa Sollievo Sofferenza Hosp, Div Gastroenterol, I-71013 San Giovanni Rotondo, ItalyIRCCS, Casa Sollievo Sofferenza Hosp, Div Gastroenterol, I-71013 San Giovanni Rotondo, Italy
Quitadamo, M
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Andriulli, A
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IRCCS, Casa Sollievo Sofferenza Hosp, Div Gastroenterol, I-71013 San Giovanni Rotondo, ItalyIRCCS, Casa Sollievo Sofferenza Hosp, Div Gastroenterol, I-71013 San Giovanni Rotondo, Italy
Andriulli, A
[1
]
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[1] IRCCS, Casa Sollievo Sofferenza Hosp, Div Gastroenterol, I-71013 San Giovanni Rotondo, Italy
Background: The ideal treatment for patients who have failed eradication of Helicobacter pylori infection after standard proton pump inhibitor-based triple therapies has still to be determined. Although either a second course of triple therapy or a quadruple therapy (proton pump inhibitor plus bismuth-based triple therapy) has been proposed, the efficacy of these second-line therapies is relatively unknown. Therefore, alternative strategies are needed. Aim: To assess the efficacy and tolerability of rifabutin, a derivative of rifamycin-S, in patients who were still H. pylori infected after two or more courses of 1-week triple therapies. Methods: Patients were given a 1-week regimen of pantoprazole 40 mg b.d. + amoxycillin 1 g b.d. + rifabutin 300 mg daily. Side-effects and compliance were determined at the end of therapy. Eradication rate was assessed with a C-13-urea breath test performed at 4 and 12 weeks after treatment. Results: Forty-one patients (mean age 47 +/- 15 years) were studied. All patients took medications according to the proposed schedule. Side-effects were infrequent and mild. The eradication rates were 71% (95% CI: 57-85%) on intention-to-treat analysis and 74% (95% CI: 61-88%) on per protocol analysis. Conclusions: Rifabutin, in combination with pantoprazole and amoxycillin, is an effective and well tolerated regimen in patients who failed standard eradication treatments.