Savarino V, Mela G S, Zentilin P, Sumberaz A, Bonifacino G, Celle G
Istituto Scientifico di Medicina Interna, Università di Genova, Italy.
Am J Gastroenterol. 1991 Mar;86(3):281-4.
To assess whether there is rebound of gastric acidity after a short-term course of H2-receptor antagonists, we performed a 24-h in situ pH monitoring on 17 duodenal ulcer patients before, during, and after completing 4 wks' treatment with nizatidine 300 mg at bedtime (2200 h). Three around-the-clock continuous intragastric pH-metries were carried out the day before beginning treatment, at the end of the nizatidine course, and 67 h after the last dose of the drug was given. Nizatidine produced mean pH values that were significantly higher (p less than 0.001) than those of the pretreatment profile during both the whole 24-h period and the nighttime (2400-0759), and this confirms that it effectively inhibited gastric acidity. Conversely, there was no significant difference between the acidity indexes of pH profiles obtained before dosing and after discontinuing treatment in any of the time intervals considered. Therefore, it appears that a short term course of nizatidine therapy does not cause rebound hyperacidity in duodenal ulcer patients.
为评估短期使用H2受体拮抗剂后胃酸是否会反弹,我们对17例十二指肠溃疡患者进行了24小时原位pH监测,监测时间为睡前(22:00)服用300毫克尼扎替丁4周治疗前、治疗期间及治疗后。在开始治疗前一天、尼扎替丁疗程结束时以及最后一剂药物服用后67小时进行了三次24小时连续胃内pH测量。尼扎替丁在整个24小时期间和夜间(24:00 - 07:59)产生的平均pH值均显著高于治疗前水平(p < 0.001),这证实了它能有效抑制胃酸。相反,在任何考虑的时间间隔内,给药前和停药后获得的pH曲线酸度指数之间均无显著差异。因此,看来短期尼扎替丁治疗不会导致十二指肠溃疡患者胃酸反跳性增高。