Hybrid vs sequential therapy for eradication of Helicobacter pylori in Taiwan: a prospective randomized trial

被引:26
作者
Chen, Kuan-Yang [1 ,2 ,3 ]
Lin, Tsung-Jung [3 ]
Lin, Chin-Lin [3 ]
Lee, Hsi-Chang [3 ]
Wang, Chung-Kwe [3 ]
Wu, Deng-Chyang [4 ,5 ,6 ,7 ,8 ]
机构
[1] Natl Yang Ming Univ, Inst Clin Med, Taipei 10629, Taiwan
[2] Natl Chengchi Univ, Inst Neurosci, Taipei 11651, Taiwan
[3] Taipei City Hosp, Ren Ai Branch, Dept Gastroenterol, Ctr Liver, Taipei 10629, Taiwan
[4] Kaohsiung Med Univ Hosp, Dept Internal Med, Div Gastroenterol, Kaohsiung 80708, Taiwan
[5] Kaohsiung Med Univ, Kaohsiung Municipal Hsiao Kang Hosp, Div Internal Med, Kaohsiung 80708, Taiwan
[6] Kaohsiung Med Univ Hosp, Ctr Stem Cell Res, Kaohsiung 80708, Taiwan
[7] Kaohsiung Med Univ, Coll Med, Fac Med, Dept Med, Kaohsiung 80708, Taiwan
[8] Kaohsiung Med Univ, Ctr Infect Dis & Canc Res, Kaohsiung 80708, Taiwan
关键词
Helicobacter pylori; Sequential therapy; Hybrid therapy; PROTON PUMP INHIBITOR; TRIPLE THERAPY; GASTRIC-CANCER; INFECTION; ULCER; CONCOMITANT; MANAGEMENT; DIAGNOSIS; REGIMENS; FAILURE;
D O I
10.3748/wjg.v21.i36.10435
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
AIM: To evaluate the efficacy of sequential vs hybrid therapy in patients with Helicobacter pylori (H. pylori) infection. METHODS: From March 2013 to May 2014, one hundred and seventy-five H. pylori infected patients who had not been treated for H. pylori before were randomized to receive either sequential therapy (rabeprazole 20 mg and amoxicillin 1 g twice daily for 5 d, followed by rabeprazole 20 mg, clarithromycin 500 mg and metronidazole 500 mg twice daily for 5 d) or hybrid therapy (rabeprazole 20 mg and amoxicillin 1 g for 7 d, followed by rabeprazole 20 mg, amoxicillin 1 g, clarithromycin 500 mg and metronidazole 500 mg twice daily for 7 d). H. pylori status was confirmed by positive results of both rapid urease test and histology examination or a positive result of culture. Eradication efficacy was assessed by follow-up endoscopy with rapid urease test and histological examination 8 wk after the end of anti-H. pylori therapy, or C-13-urea breath test at least 4 wk after completion of treatment. The primary outcome was H. pylori eradication by intension-to-treat (ITT) and per-protocol (PP) analyses. RESULTS: One hundred and sixty-seven patients (83 patients in the sequential group and 84 patients in the hybrid group) completed the study. The compliance rates were 97.6% and 97.7% for the two groups, respectively. The eradication rate was 78.2% for the sequential group and 92% for the hybrid group by ITT analysis (P = 0.01). The eradication rate was 81.9% for the sequential group and 96.4% for the hybrid group by PP analysis (P = 0.01). Univariate analysis for the clinical and bacterial factors did not identify any risk factors associated with treatment failure. Severe adverse events were observed in 2.3% of patients in the sequential group and 2.4% of those in the hybrid group. CONCLUSION: Due to a grade A (> 95%) success rate for H. pylori eradication by PP analysis, similar compliance and adverse events, hybrid therapy seems to be an appropriate eradication regimen in Taiwan.
引用
收藏
页码:10435 / 10442
页数:8
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