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Article: Ten day sequential versus 10 day modified bismuth quadruple therapy as empirical firstline and secondline treatment for Helicobacter pylori in Chinese patients: an open label, randomised, crossover trial

TitleTen day sequential versus 10 day modified bismuth quadruple therapy as empirical firstline and secondline treatment for Helicobacter pylori in Chinese patients: an open label, randomised, crossover trial
Authors
Keywords13C-Urea Breath Test
Antibiotics
Helicobacter Pylori - Treatment
Issue Date2014
PublisherBMJ Publishing Group. The Journal's web site is located at http://gut.bmjjournals.com/
Citation
Gut, 2014, v. 63 n. 9, p. 1410-1415 How to Cite?
AbstractOBJECTIVE: Treatments with sequential therapy (SEQ) or bismuth quadruple (QUAD) therapy have been proposed as empirical firstline regimens for Helicobacter pylori. We compared the efficacy and tolerability of 10 day SEQ with 10 day modified QUAD as both firstline and secondline treatments for H pylori in a randomised crossover study. DESIGN: H pylori positive and treatment naive patients were randomly assigned to receive either 10 day SEQ (esomeprazole for 10 days, amoxicillin for an initial 5 days, followed by clarithromycin and metronidazole for a subsequent 5 days) or modified QUAD (esomeprazole, bismuth subcitrate, tetracycline and metronidazole). H pylori eradication was confirmed by urea breath test at 8 weeks. Patients who failed the initial assigned treatment were crossed over to receive the alternate regimen. The primary outcome was eradication rates of firstline treatment by intention to treat (ITT) and per protocol (PP) analyses. RESULTS: 357 patients were randomised to receive either SEQ or QUAD. The PP eradication rates of the SEQ and QUAD groups were 95.2% and 98.8%, respectively (p=0.10). Based on ITT analysis, the corresponding eradication rates were 89.4% and 92.7%, respectively (p=0.36). Eight (4.8%) patients in the SEQ and two (1.2%) patients in the QUAD who failed the firstline treatment were crossed over to the alternate regimen with 100% retreatment success. The overall incidence of adverse events was higher in the QUAD (16.7%) than in the SEQ (8.1%; p=0.032) group. CONCLUSIONS: Ten day sequential and modified bismuth quadruple therapies are both highly effective as empirical firstline therapies for H pylori in Chinese patients. CLINICALTRIALS.GOV: NCT 01760824.
Persistent Identifierhttp://hdl.handle.net/10722/193877
ISSN
2021 Impact Factor: 31.793
2020 SCImago Journal Rankings: 8.413
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLiu, KSH-
dc.contributor.authorHung, IFN-
dc.contributor.authorSeto, WKW-
dc.contributor.authorTong, T-
dc.contributor.authorHsu, ASJ-
dc.contributor.authorLam, FYF-
dc.contributor.authorBut, DYK-
dc.contributor.authorWong, SY-
dc.contributor.authorLeung, WK-
dc.date.accessioned2014-01-28T06:30:45Z-
dc.date.available2014-01-28T06:30:45Z-
dc.date.issued2014-
dc.identifier.citationGut, 2014, v. 63 n. 9, p. 1410-1415-
dc.identifier.issn0017-5749-
dc.identifier.urihttp://hdl.handle.net/10722/193877-
dc.description.abstractOBJECTIVE: Treatments with sequential therapy (SEQ) or bismuth quadruple (QUAD) therapy have been proposed as empirical firstline regimens for Helicobacter pylori. We compared the efficacy and tolerability of 10 day SEQ with 10 day modified QUAD as both firstline and secondline treatments for H pylori in a randomised crossover study. DESIGN: H pylori positive and treatment naive patients were randomly assigned to receive either 10 day SEQ (esomeprazole for 10 days, amoxicillin for an initial 5 days, followed by clarithromycin and metronidazole for a subsequent 5 days) or modified QUAD (esomeprazole, bismuth subcitrate, tetracycline and metronidazole). H pylori eradication was confirmed by urea breath test at 8 weeks. Patients who failed the initial assigned treatment were crossed over to receive the alternate regimen. The primary outcome was eradication rates of firstline treatment by intention to treat (ITT) and per protocol (PP) analyses. RESULTS: 357 patients were randomised to receive either SEQ or QUAD. The PP eradication rates of the SEQ and QUAD groups were 95.2% and 98.8%, respectively (p=0.10). Based on ITT analysis, the corresponding eradication rates were 89.4% and 92.7%, respectively (p=0.36). Eight (4.8%) patients in the SEQ and two (1.2%) patients in the QUAD who failed the firstline treatment were crossed over to the alternate regimen with 100% retreatment success. The overall incidence of adverse events was higher in the QUAD (16.7%) than in the SEQ (8.1%; p=0.032) group. CONCLUSIONS: Ten day sequential and modified bismuth quadruple therapies are both highly effective as empirical firstline therapies for H pylori in Chinese patients. CLINICALTRIALS.GOV: NCT 01760824.-
dc.languageeng-
dc.publisherBMJ Publishing Group. The Journal's web site is located at http://gut.bmjjournals.com/-
dc.relation.ispartofGut-
dc.subject13C-Urea Breath Test-
dc.subjectAntibiotics-
dc.subjectHelicobacter Pylori - Treatment-
dc.titleTen day sequential versus 10 day modified bismuth quadruple therapy as empirical firstline and secondline treatment for Helicobacter pylori in Chinese patients: an open label, randomised, crossover trial-
dc.typeArticle-
dc.identifier.emailHung, IFN: ivanhung@hkucc.hku.hk-
dc.identifier.emailSeto, WKW: wkseto2@hku.hk-
dc.identifier.emailHsu, ASJ: axelhsu@hku.hk-
dc.identifier.emailLam, FYF: fyflam@hku.hk-
dc.identifier.emailBut, DYK: drdbut@hku.hk-
dc.identifier.emailWong, SY: ksywong@hkucc.hku.hk-
dc.identifier.emailLeung, WK: hku75407@hku.hk-
dc.identifier.authorityHung, IFN=rp00508-
dc.identifier.authoritySeto, WKW=rp01659-
dc.identifier.authorityLam, FYF=rp02564-
dc.identifier.authorityLeung, WK=rp01479-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1136/gutjnl-2013-306120-
dc.identifier.pmid24295850-
dc.identifier.scopuseid_2-s2.0-84905440362-
dc.identifier.hkuros227483-
dc.identifier.volume63-
dc.identifier.issue9-
dc.identifier.spage1410-
dc.identifier.epage1415-
dc.identifier.isiWOS:000341014600012-
dc.publisher.placeUnited Kingdom-
dc.identifier.issnl0017-5749-

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