Phull P S, Price A B, Halliday D, Jacyna M R
Department of Gastroenterology, Northwick Park Hospital, Harrow, Middlesex.
Br J Clin Pract. 1996 Oct-Nov;50(7):360-2.
The aim of this pilot study was to evaluate the efficacy and safety of lansoprazole plus clarithromycin for eradication of Helicobacter pylori. A total of 26 patients with H. pylori infection were randomised to receive clarithromycin, 500 mg t.i.d. for 14 days, plus either lansoprazole, 30 mg o.m., (group L30, n = 13) or lansoprazole, 30 mg b.i.d., (group L60, n = 13). H. pylori status was determined pre-treatment and four to six weeks after completion of the study medication by histology and 13C-urea breath test. Two patients were unable to complete the course of medication. Of the remaining 24 patients, 14 (58%) successfully eradicated H. pylori--8/12 (67%) patients in group L30 and 6/12 (50%) in group L60. Side-effects were experienced by 17/26 (65%) of patients, most commonly a taste disturbance. The results from this pilot study suggest that dual therapy with lansoprazole plus clarithromycin is only a moderately effective regimen for eradicating H. pylori.
这项初步研究的目的是评估兰索拉唑联合克拉霉素根除幽门螺杆菌的疗效和安全性。共有26例幽门螺杆菌感染患者被随机分为两组,一组接受克拉霉素,500毫克,每日三次,共14天,加兰索拉唑,30毫克,每日一次(L30组,n = 13);另一组接受兰索拉唑,30毫克,每日两次(L60组,n = 13)。在治疗前以及完成研究用药后的四至六周,通过组织学检查和13C - 尿素呼气试验确定幽门螺杆菌状态。两名患者未能完成疗程。在其余24例患者中,14例(58%)成功根除幽门螺杆菌——L30组12例中有8例(67%),L60组12例中有6例(50%)。26例患者中有17例(65%)出现副作用,最常见的是味觉障碍。这项初步研究的结果表明,兰索拉唑联合克拉霉素的双重疗法仅是一种中度有效的根除幽门螺杆菌的方案。