Sequential therapy versus standard triple-drug therapy for Helicobacter pylori eradication: a randomized trial
- PMID: 17438314
- DOI: 10.7326/0003-4819-146-8-200704170-00006
Sequential therapy versus standard triple-drug therapy for Helicobacter pylori eradication: a randomized trial
Abstract
Background: Antimicrobial resistance has decreased eradication rates for Helicobacter pylori infection worldwide.
Objective: To determine whether sequential treatment eradicates H. pylori infection better than standard triple-drug therapy for adults with dyspepsia or peptic ulcers.
Design: Randomized, double-blind, placebo-controlled trial.
Setting: Two Italian hospitals between September 2003 and April 2006.
Patients: 300 patients with dyspepsia or peptic ulcers.
Measurements: (13)C-urea breath test, upper endoscopy, histologic evaluation, rapid urease test, bacterial culture, and assessment of antibiotic resistance.
Intervention: A 10-day sequential regimen (40 mg of pantoprazole, 1 g of amoxicillin, and placebo, each administered twice daily for the first 5 days, followed by 40 mg of pantoprazole, 500 mg of clarithromycin, and 500 mg of tinidazole, each administered twice daily for the remaining 5 days) or standard 10-day therapy (40 mg of pantoprazole, 500 mg of clarithromycin, and 1 g of amoxicillin, each administered twice daily).
Results: The eradication rate achieved with the sequential regimen was significantly greater than that obtained with the standard treatment in the intention-to-treat analysis (89% vs. 77%; P = 0.0134; difference, 12% [95% CI, 3% to 20%]), the modified intention-to-treat analysis (91% vs. 78%; P = 0.0022; difference, 13% [CI, 5% to 21%]), and the per-protocol analysis (93% vs. 79%; P = 0.0013; difference, 14% [CI, 6% to 21%]). Sequential therapy was significantly more effective in patients with clarithromycin-resistant strains (89% vs. 29%; P = 0.0034). The incidence of major and minor side effects did not differ between therapy groups (17% in both groups). One patient (0.7%) in the standard therapy group discontinued treatment because of side effects.
Limitations: Follow-up was incomplete in 4.6% and 2.7% patients in the sequential therapy and standard therapy groups, respectively. The results may not be generalizable to other countries. Sequential therapy may be more effective because it includes 1 additional antibiotic (tinidazole) that is not contained in standard therapy.
Conclusions: Sequential therapy is statistically significant compared with standard therapy for eradicating H. pylori infection and is statistically significantly more effective in patients with clarithromycin-resistant strains. Side effects are similar with both treatment regimens and are rarely severe enough to cause discontinuation of therapy. ClinicalTrials.gov registration number: NCT00403364.
Comment in
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Switching antibiotics mid-course improves H. pylori cure rate.J Fam Pract. 2007 Aug;56(8):608. J Fam Pract. 2007. PMID: 17674449 No abstract available.
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10-day sequential therapy was more effective than 10-day triple-drug therapy for eradicating Helicobacter pylori infection.ACP J Club. 2007 Sep-Oct;147(2):40. ACP J Club. 2007. PMID: 17764131 No abstract available.
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Ethical considerations of comparing sequential and traditional anti Helicobacter pylori therapy.Ann Intern Med. 2007 Sep 18;147(6):434-5. doi: 10.7326/0003-4819-147-6-200709180-00022. Ann Intern Med. 2007. PMID: 17876031 No abstract available.
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10 day sequential therapy was more effective than 10 day triple drug therapy for eradicating Helicobacter pylori infection.Evid Based Med. 2007 Oct;12(5):146. doi: 10.1136/ebm.12.5.146. Evid Based Med. 2007. PMID: 17909237 No abstract available.
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New developments in the treatment of Helicobacter pylori: is sequential therapy the answer?Rev Gastroenterol Disord. 2008 Summer;8(3):217-8. Rev Gastroenterol Disord. 2008. PMID: 18957929 No abstract available.
Summary for patients in
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Summaries for patients. Sequential therapy versus standard triple-drug therapy for Helicobacter pylori eradication.Ann Intern Med. 2007 Apr 17;146(8):I20. doi: 10.7326/0003-4819-146-8-200704170-00002. Ann Intern Med. 2007. PMID: 17438311 No abstract available.
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