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14 day sequential therapy versus 10 day bismuth quadruple therapy containing high-dose esomeprazole in the first-line and second-line treatment of Helicobacter pylori: a multicentre, non-inferiority, randomized trial.
Liou, Jyh-Ming; Chen, Chieh-Chang; Fang, Yu-Jen; Chen, Po-Yueh; Chang, Chi-Yang; Chou, Chu-Kuang; Chen, Mei-Jyh; Tseng, Cheng-Hao; Lee, Ji-Yuh; Yang, Tsung-Hua; Chiu, Min-Chin; Yu, Jian-Jyun; Kuo, Chia-Chi; Luo, Jiing-Chyuan; Hsu, Wen-Feng; Hu, Wen-Hao; Tsai, Min-Horn; Lin, Jaw-Town; Shun, Chia-Tung; Twu, Gary; Lee, Yi-Chia; Bair, Ming-Jong; Wu, Ming-Shiang.
Affiliation
  • Liou JM; Division of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
  • Chen CC; Department of Internal Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan.
  • Fang YJ; Division of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
  • Chen PY; Department of Internal Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan.
  • Chang CY; Department of Internal Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan.
  • Chou CK; Department of Internal Medicine, National Taiwan University Hospital, Yun-Lin Branch, Yun-Lin, Taiwan.
  • Chen MJ; Division of Gastroenterology and Hepatology, Department of Internal Medicine, Chia-Yi Christian Hospital, Chia-Yi, Taiwan.
  • Tseng CH; School of Medicine, Fu Jen Catholic University, New Taipei City, Taiwan.
  • Lee JY; Department of Internal Medicine, E-DA Hospital and I-Shou University, Kaohsiung, Taiwan.
  • Yang TH; Division of Gastroenterology and Hepatology, Department of Internal Medicine, Chia-Yi Christian Hospital, Chia-Yi, Taiwan.
  • Chiu MC; Division of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
  • Yu JJ; Department of Internal Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan.
  • Kuo CC; School of Medicine, Fu Jen Catholic University, New Taipei City, Taiwan.
  • Luo JC; Department of Internal Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan.
  • Hsu WF; Department of Internal Medicine, National Taiwan University Hospital, Yun-Lin Branch, Yun-Lin, Taiwan.
  • Hu WH; Department of Internal Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan.
  • Tsai MH; Department of Internal Medicine, National Taiwan University Hospital, Yun-Lin Branch, Yun-Lin, Taiwan.
  • Lin JT; Department of Internal Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan.
  • Shun CT; Department of Internal Medicine, National Taiwan University Hospital, Yun-Lin Branch, Yun-Lin, Taiwan.
  • Twu G; Department of Internal Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan.
  • Lee YC; Department of Internal Medicine, National Taiwan University Hospital, Yun-Lin Branch, Yun-Lin, Taiwan.
  • Bair MJ; Department of Internal Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan.
  • Wu MS; Department of Internal Medicine, National Taiwan University Hospital, Yun-Lin Branch, Yun-Lin, Taiwan.
J Antimicrob Chemother ; 73(9): 2510-2518, 2018 09 01.
Article in En | MEDLINE | ID: mdl-29846605
ABSTRACT

Background:

Whether extending the treatment length and the use of high-dose esomeprazole may optimize the efficacy of Helicobacter pylori eradication remains unknown.

Objectives:

To compare the efficacy and tolerability of optimized 14 day sequential therapy and 10 day bismuth quadruple therapy containing high-dose esomeprazole in first-line therapy.

Methods:

We recruited 620 adult patients (≥20 years of age) with H. pylori infection naive to treatment in this multicentre, open-label, randomized trial. Patients were randomly assigned to receive 14 day sequential therapy or 10 day bismuth quadruple therapy, both containing esomeprazole 40 mg twice daily. Those who failed after 14 day sequential therapy received rescue therapy with 10 day bismuth quadruple therapy and vice versa. Our primary outcome was the eradication rate in the first-line therapy. Antibiotic susceptibility was determined. ClinicalTrials.gov NCT03156855.

Results:

The eradication rates of 14 day sequential therapy and 10 day bismuth quadruple therapy were 91.3% (283 of 310, 95% CI 87.4%-94.1%) and 91.6% (284 of 310, 95% CI 87.8%-94.3%) in the ITT analysis, respectively (difference -0.3%, 95% CI -4.7% to 4.4%, P = 0.886). However, the frequencies of adverse effects were significantly higher in patients treated with 10 day bismuth quadruple therapy than those treated with 14 day sequential therapy (74.4% versus 36.7% P < 0.0001). The eradication rate of 14 day sequential therapy in strains with and without 23S ribosomal RNA mutation was 80% (24 of 30) and 99% (193 of 195), respectively (P < 0.0001).

Conclusions:

Optimized 14 day sequential therapy was non-inferior to, but better tolerated than 10 day bismuth quadruple therapy and both may be used in first-line treatment in populations with low to intermediate clarithromycin resistance.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bismuth / Helicobacter Infections / Esomeprazole / Antacids / Anti-Ulcer Agents / Anti-Bacterial Agents Type of study: Clinical_trials Limits: Adult / Aged / Aged80 / Humans / Middle aged Language: En Journal: J Antimicrob Chemother Year: 2018 Type: Article Affiliation country: Taiwan

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bismuth / Helicobacter Infections / Esomeprazole / Antacids / Anti-Ulcer Agents / Anti-Bacterial Agents Type of study: Clinical_trials Limits: Adult / Aged / Aged80 / Humans / Middle aged Language: En Journal: J Antimicrob Chemother Year: 2018 Type: Article Affiliation country: Taiwan