Savarino V, Mela G S, Scalabrini P, Di Timoteo E, Magnolia M R, Celle G
Digestion. 1987;37(2):103-9. doi: 10.1159/000199475.
In 11 duodenal ulcer patients, the antisecretory effects of bedtime famotidine 40 mg were compared to those obtained with ranitidine 300 mg and placebo by means of continuous 24-hour intragastric pH monitoring. The 24-hour areas under the curve of pH profiles of the two H2 blockers were significantly different from those related to placebo (p approximately 0 for ranitidine and p = 0.00001 for famotidine), but not from each other (p = 0.51). Onset and duration of the famotidine action, however, were respectively earlier and longer lasting (12 vs. about 9 h) than those of ranitidine. Famotidine was also significantly superior (p approximately 0) to ranitidine in keeping intragastric pH at high values (especially those comprised between 6 and 8 pH units), although theoretically equipotent doses of the two H2 antagonists were used.
在11例十二指肠溃疡患者中,通过连续24小时胃内pH监测,比较了睡前服用40毫克法莫替丁与服用300毫克雷尼替丁及安慰剂的抑酸效果。两种H2受体阻滞剂的24小时pH曲线下面积与安慰剂相关的曲线下面积有显著差异(雷尼替丁p约为0,法莫替丁p = 0.00001),但两者之间无显著差异(p = 0.51)。然而,法莫替丁作用的起效时间和持续时间分别比雷尼替丁更早且更持久(12小时对约9小时)。尽管理论上使用的两种H2拮抗剂剂量等效,但在使胃内pH保持在较高值(尤其是pH值在6至8单位之间)方面,法莫替丁也显著优于雷尼替丁(p约为0)。