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2016 ; 65
(11
): 1784-1792
Nephropedia Template TP
gab.com Text
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Twit Text #
English Wikipedia
Sequential therapy for 10?days versus triple therapy for 14?days in the
eradication of Helicobacter pylori in the community and hospital populations: a
randomised trial
#MMPMID26338825
Liou JM
; Chen CC
; Chang CY
; Chen MJ
; Chen CC
; Fang YJ
; Lee JY
; Yang TH
; Luo JC
; Wu JY
; Liou TC
; Chang WH
; Hsu YC
; Tseng CH
; Chang CC
; Bair MJ
; Liu TY
; Hsieh CF
; Tsao FY
; Shun CT
; Lin JT
; Lee YC
; Wu MS
Gut
2016[Nov]; 65
(11
): 1784-1792
PMID26338825
show ga
OBJECTIVE: Significant heterogeneity was observed in previous trials that
assessed the efficacies of sequential therapy for 10?days (S10) versus triple
therapy for 14?days (T14) in the first-line treatment of Helicobacter pylori. We
aimed to compare the efficacy of S10 and T14 and assess the factors affecting
their efficacies. DESIGN: We conducted this open-label randomised multicentre
trial in eight hospitals and one community in Taiwan. 1300 adult subjects with H
pylori infection naïve to treatment were randomised (1:1) to receive S10
(lansoprazole and amoxicillin for the first 5?days, followed by lansoprazole,
clarithromycin and metronidazole for another 5?days) or T14 (lansoprazole,
amoxicillin and clarithromycin for 14?days). All drugs were given twice daily.
Successful eradication was defined as negative (13)C-urea breath test at least
6?weeks after treatment. Our primary outcome was the eradication rate by
intention-to-treat (ITT) and per-protocol (PP) analyses. Antibiotic resistance
was determined by agar dilution test. RESULTS: The eradication rates of S10 and
T14 were 87.2% (567/650, 95% CI 84.4% to 89.6%) and 85.7% (557/650, 95% CI 82.8%
to 88.2%) in the ITT analysis, respectively, and were 91.6% (556/607, 95% CI
89.1% to 93.4%) and 91.0% (548/602, 95% CI 88.5% to 93.1%) in the PP analysis,
respectively. There were no differences in compliance or adverse effects. The
eradication rates in strains susceptible and resistant to clarithromycin were
90.7% and 62.2%, respectively, for S10, and were 91.5% and 44.4%, respectively,
for T14. The efficacy of T14, but not S10, was affected by CYP2C19 polymorphism.
CONCLUSIONS: S10 was not superior to T14 in areas with low clarithromycin
resistance. TRIAL REGISTRATION NUMBER: NCT01607918.