Department of Gastroenterology, Daping Hospital, The Army Medical University, Chongqing, China.
Am J Gastroenterol. 2019 Mar;114(3):437-445. doi: 10.14309/ajg.0000000000000132.
This study assessed the effectiveness, adverse events, patient adherence, and costs of modified dual therapy compared with bismuth-containing quadruple therapy for treating Helicobacter pylori infection in Chinese patients. We also sought to determine whether modified dual therapy could be used as an alternative first-line treatment for H. pylori infection.
A total of 232 H. pylori-infected, treatment-naive patients were enrolled in this open-label, randomized controlled clinical trial. Patients were randomly allocated into 2 groups: the 14-day modified dual therapy group and the bismuth-containing quadruple therapy group. Eradication rates, drug-related adverse events, patient compliance, and drug costs were compared between the 2 groups.
The modified dual therapy group achieved eradication rates of 87.9%, 91.1%, and 91.1% as determined by the intention-to-treat, per-protocol, and modified intention-to-treat analyses, respectively. The eradication rates were similar compared with the bismuth-containing quadruple therapy group: 89.7%, 91.2%, and 90.4%. In addition, modified dual therapy ameliorated variations in the CYP2C19, IL-1B-511, and H. pylori VacA genotypes. There were no significant differences in the compliance rates between the 2 groups. The modified dual therapy group exhibited significantly less overall side effects compared with the bismuth-containing quadruple therapy group (P < 0.001). Furthermore, the cost of medications in the modified dual therapy was lower compared with that in the bismuth-containing quadruple therapy.
Modified dual therapy at high dose and administration frequency is equally effective and safer and less costly compared with bismuth-containing quadruple therapy.
本研究评估了改良双联疗法与含铋四联疗法治疗中国幽门螺杆菌感染的疗效、不良反应、患者依从性和成本,旨在确定改良双联疗法是否可作为幽门螺杆菌感染的一线替代治疗方案。
这是一项开放标签、随机对照临床试验,共纳入 232 例未经治疗的幽门螺杆菌感染初治患者。患者被随机分为两组:14 天改良双联疗法组和含铋四联疗法组。比较两组的根除率、药物相关不良反应、患者依从性和药物成本。
意向治疗、符合方案和改良意向治疗分析的改良双联疗法组根除率分别为 87.9%、91.1%和 91.1%,与含铋四联疗法组的根除率(89.7%、91.2%和 90.4%)相似。此外,改良双联疗法改善了 CYP2C19、IL-1B-511 和幽门螺杆菌 VacA 基因型的变异。两组的依从率无显著差异。改良双联疗法组的总体不良反应发生率明显低于含铋四联疗法组(P<0.001)。此外,改良双联疗法的药物总成本低于含铋四联疗法。
高剂量和高频率的改良双联疗法与含铋四联疗法疗效相当,且安全性更高,成本更低。