Attumi Taraq A, Graham David Y
Michael E. DeBakey Veterans Affairs Medical Center, RM 3A-320 (111D), 2002 Holcombe Boulevard and Baylor College of Medicine, Houston, TX, 77030, USA.
Helicobacter. 2014 Aug;19(4):319-22. doi: 10.1111/hel.12126. Epub 2014 Apr 3.
Helicobacter pylori infections have become increasingly difficult to treat.
To examine whether amoxicillin and high-dose dexlansoprazole would reliably achieve an H. pylori eradication rate of ≥90%.
An open-label prospective pilot study of H. pylori eradication in treatment-naïve subjects with active H. pylori infection (positive by two tests).
amoxicillin 1 g and dexlansoprazole 120 mg each twice a day at approximately 12-hour intervals for 14 days. Success was accessed by urea breath test. An effective therapy was defined as a per-protocol treatment success of 90% or greater; treatment success of 80% or less was prespecified as an unacceptable result.
After 13 subjects were entered (12 men, one woman; average age of 54 years), the prespecified stopping rule of six treatment failures was achieved (i.e., the 95% confidence interval excluded achieving the required 90% success rate even if the proposed study of 50 completed patients were entered) and enrollment was stopped. Per-protocol and intention-to-treat treatment success were both 53.8%; (7/13); 95% CI = 25-80%. Compliance was 100%. Three patients (23%) reported side effects, all of which were mild and none interrupted therapy.
Theoretically, dual PPI plus amoxicillin should reliably eradicate H. pylori provided nearly neutral intragastric pH can be maintained. Clearly, dexlansoprazole, despite being administered at high dose and twice a day (i.e., total daily dose 240 mg), failed to achieve an intragastric milieu consistent with dual PPI plus amoxicillin therapy being an effective anti-H. pylori regimen.
幽门螺杆菌感染的治疗难度日益增大。
探讨阿莫西林和高剂量右兰索拉唑能否可靠地实现幽门螺杆菌根除率≥90%。
一项针对初治的活动性幽门螺杆菌感染受试者(两种检测均为阳性)进行的幽门螺杆菌根除开放标签前瞻性试验研究。
阿莫西林1克和右兰索拉唑120毫克,均每日两次,间隔约12小时,共治疗14天。通过尿素呼气试验评估治疗效果。有效治疗定义为符合方案治疗成功率达到90%或更高;治疗成功率为80%或更低则预先设定为不可接受的结果。
纳入13名受试者(12名男性,1名女性;平均年龄54岁)后,达到了预先设定的6例治疗失败的停止规则(即即使纳入拟研究的50例完成患者,95%置信区间也排除了达到所需90%成功率的可能性),于是停止入组。符合方案和意向性治疗的治疗成功率均为53.8%(7/13);95%置信区间=25 - 80%。依从性为100%。3名患者(23%)报告有副作用,均为轻度,无一例中断治疗。
理论上,双重质子泵抑制剂加阿莫西林应能可靠地根除幽门螺杆菌,前提是能维持胃内pH值接近中性。显然,尽管右兰索拉唑大剂量每日两次给药(即每日总剂量240毫克),但仍未能实现与双重质子泵抑制剂加阿莫西林疗法作为有效的抗幽门螺杆菌方案相一致的胃内环境。