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奥美拉唑20毫克每周三次、10毫克每日一次用于预防十二指肠溃疡复发。双盲对照试验。

Omeprazole 20 mg three days a week and 10 mg daily in prevention of duodenal ulcer relapse. Double-blind comparative trial.

作者信息

Lauritsen K, Andersen B N, Laursen L S, Hansen J, Havelund T, Eriksen J, Rehfeld J F, Kjaergaard J, Rask-Madsen J

机构信息

Department of Medical Gastroenterology, Odense University Hospital, Denmark.

出版信息

Gastroenterology. 1991 Mar;100(3):663-9. doi: 10.1016/0016-5085(91)80009-x.

Abstract

In a double-blind, parallel-group clinical trial of 195 patients with duodenal ulcers who after a short-term study had relief of pain and healed ulcers proved endoscopically, 65 were randomized to receive 20 mg omeprazole 3 days a week (once in the morning from Friday to Sunday), 64 to receive 10 mg omeprazole once daily in the morning, and 66 to receive placebo for up to 6 months. The patients underwent repeat endoscopy with biopsy of the gastric fundic mucosa (qualitative assessment of argyrophilic cell population), assessment of symptoms, and laboratory screening with measurement of basal serum gastrin concentrations at 3 and 6 months or more often if indicated by recurrence of symptoms. At 3 months, endoscopically proved ulcer relapse occurred in 16% receiving 20 mg omeprazole 3 days a week; 21% receiving 10 mg omeprazole daily; and 50% receiving placebo. At 6 months, corresponding rates were 23%, 27%, and 67% with 95% confidence intervals of difference between the placebo group and omeprazole groups of 28%-60% and 24%-56% (P less than 0.00001), respectively, and between omeprazole groups of -19%-11% (NS). No major clinical or laboratory side effects were noted. Thus both omeprazole regimens are effective and safe in preventing duodenal ulcer relapse.

摘要

在一项针对195例十二指肠溃疡患者的双盲平行组临床试验中,这些患者在短期研究后疼痛缓解且经内镜检查溃疡已愈合。65例患者被随机分配,每周3天接受20毫克奥美拉唑(周五至周日每天早晨服用一次);64例患者每天早晨接受10毫克奥美拉唑;66例患者接受安慰剂,为期6个月。患者在3个月和6个月时接受重复内镜检查并取胃底黏膜活检(嗜银细胞群体的定性评估)、症状评估以及实验室筛查,测量基础血清胃泌素浓度,若症状复发则更频繁地进行检测。3个月时,每周3天接受20毫克奥美拉唑的患者中,经内镜证实溃疡复发的比例为16%;每天接受10毫克奥美拉唑的患者中为21%;接受安慰剂的患者中为50%。6个月时,相应比例分别为23%、27%和67%,安慰剂组与奥美拉唑组之间差异的95%置信区间分别为28% - 60%和24% - 56%(P小于0.00001),奥美拉唑组之间为 - 19% - 11%(无显著性差异)。未观察到重大临床或实验室副作用。因此,两种奥美拉唑治疗方案在预防十二指肠溃疡复发方面均有效且安全。

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