Vonoprazan-amoxicillin dual therapy with different amoxicillin dosages for treatment-naive patients of Helicobacter pylori infection in China: a prospective, randomized controlled study

被引:0
|
作者
Liu, Zhu [1 ,2 ]
Sun, Dongjie [3 ]
Kou, Luan [2 ]
Jia, Li [2 ]
Hao, Jiaorong [2 ]
Zhou, Jihai [2 ]
Zheng, Wenwen [2 ]
Gao, Fengyu [2 ]
Chen, Xin [1 ]
机构
[1] Tianjin Med Univ, Tianjin Inst Digest Dis, Dept Gastroenterol & Hepatol, Tianjin Key Lab Digest Dis,Gen Hosp, 154 Anshan Rd, Tianjin 300052, Peoples R China
[2] Qingdao Univ, Shandong Prov Maternal & Child Hlth Care Hosp Affi, Dept Gastroenterol, Jinan, Peoples R China
[3] Fujian Med Univ, Fuzong Clin Med Coll, Dept Digest Dis, Fuzhou, Peoples R China
关键词
amoxicillin; dual therapy; eradication rate; Helicobacter pylori; vonoprazan; ANTIBIOTIC-RESISTANCE; 1ST-LINE;
D O I
10.1097/MEG.0000000000002760
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background The vonoprazan (VPZ)-amoxicillin (AMO) dual therapy (VA) demonstrates a satisfactory eradication rate for Helicobacter pylori (H. pylori). However, the optimal dosage of AMO in this regimen remains uncertain. The objective of this study is to investigate the efficacy of different doses of AMO in the VA regimen for first-line treatment of H. pylori infection. Methods A total of 192 treatment-naive H. pylori-infected patients were randomly assigned to one of three groups: low-dose VA (LD-VA: VPZ 20 mg b.i.d + AMO 750 mg t.i.d), moderate-dose VA (MD-VA:VPZ 20 mg b.i.d + AMO 1000 mg t.i.d), and high-dose VA (HD-VA: VPZ 20 mg b.i.d + AMO 1250 mg t.i.d). All groups received 14 days of treatment. The study evaluated and compared the eradication rates, adverse events (AEs), and patient compliance among the three groups. Results Eradication rates for LD-VA, MD-VA, and HD-VA were 76.6% (49/64), 79.7% (51/64), and 84.4% (54/64), respectively, as determined by intention-to-treat analysis; 90.6% (48/53), 94.3% (50/53), and 98.1% (53/54) according to per-protocol analysis; 89.1% (49/55), 94.4% (51/54), and 96.4% (54/56) with modified intention-to-treat analysis (all P > 0.05). Although not statistically significant, numerically higher eradication rates were observed with the higher dose AMO VA regimen. There were no statistically significant differences in the incidence of AEs and compliance among the three VA regimens. Conclusion Fourteen-day VA regimens with AMO doses exceeding 2 g/day demonstrated satisfactory eradication rates. HD-VA therapy is potentially the most effective regimen. Large-sample clinical trials are required to further validate these findings. Copyright (c) 2024 Wolters Kluwer Health, Inc. All rights reserved.
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页码:712 / 719
页数:8
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