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  4. Sequential versus triple therapy for the first-line treatment of Helicobacter pylori: a multicentre, open-label, randomised trial
 
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Sequential versus triple therapy for the first-line treatment of Helicobacter pylori: a multicentre, open-label, randomised trial

Journal
LANCET
Journal Volume
381
Journal Issue
9862
Pages
205
Date Issued
2013-01
Author(s)
JYH-MING LIOU  
CHIEH-CHANG CHEN  
MEI-JYH CHEN  
CHIEN-CHUAN CHEN  
Chang, Chi-Yang
YU-JEN FANG  
Lee, Ji-Yuh
SHIH-JER HSU  
Luo, Jiing-Chyuan
Chang, Wen-Hsiung
Hsu, Yao-Chun
Tseng, Cheng-Hao
PING-HUEI TSENG  
HSIU-PO WANG  
Yang, Ueng-Cheng
CHIA-TUNG SHUN  
Lin, Jaw-Town
YI-CHIA LEE  
MING-SHIANG WU  
DOI
10.1016/S0140-6736(12)61579-7
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/628669
URL
https://api.elsevier.com/content/abstract/scopus_id/85101728276
Abstract
Background Whether sequential treatment can replace triple therapy as the standard treatment for Helicobacter pylori infection is unknown. We compared the efficacy of sequential treatment for 10 days and 14 days with triple therapy for 14 days in first-line treatment. Methods For this multicentre, open-label, randomised trial, we recruited patients (≥20 years of age) with H pylori infection from six centres in Taiwan. Using a computer-generated randomisation sequence, we randomly allocated patients (1:1:1; block sizes of six) to either sequential treatment (lansoprazole 30 mg and amoxicillin 1 g for the first 7 days, followed by lansoprazole 30 mg, clarithromycin 500 mg, and metronidazole 500 mg for another 7 days; with all drugs given twice daily) for either 10 days (S-10) or 14 days (S-14), of 14 days of triple therapy (T-14; lansoprazole 30 mg, amoxicillin 1 g, and clarithromycin 500 mg for 14 days; with all drugs given twice daily). Investigators were masked to treatment allocation. Our primary outcome was the eradication rate in first-line treatment by intention-totreat (ITT) and per-protocol (PP) analyses. This trial is registered with ClinicalTrials.gov, number NCT01042184. Findings Between Dec 28, 2009, and Sept 24, 2011, we enrolled 900 patients: 300 to each group. The eradication rate was 90.7% (95% CI 87.4.94.0; 272 of 300 patients) in the S-14 group, 87.0% (83.2.90.8; 261 of 300 patients) in the S-10 group, and 82.3% (78.0.86.6; 247 of 300 patients) in the T-14 group. Treatment efficacy was better in the S-14 group than it was in the T-14 group in both the ITT analysis (number needed to treat of 12.0 [95% CI 7.2.34.5]; p=0.003) and PP analyses (13.7 [8.3.40], p=0.003). We recorded no significant difference in the occurrence of adverse effects or in compliance between the three groups. Interpretation Our findings lend support to the use of sequential treatment as the standard first-line treatment for H pylori infection.
Subjects
ERADICATION THERAPY; CLINICAL-TRIAL; INFECTION; METAANALYSIS; LEVOFLOXACIN; RESISTANCE; MANAGEMENT; DIAGNOSIS; GENOTYPES; CHILDREN
Publisher
ELSEVIER SCIENCE INC
Type
journal article

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