Simon B, Dammann H G, Müller P
Medizinische Universitätsklinik Heidelberg, Abteilung für Gastroenterologie.
Z Gastroenterol. 1987 Aug;25 Suppl 3:146-51.
Omeprazole is a substituted benzimidazole which inhibits profoundly and long-lasting human acid secretion. The maximum inhibition effect of omeprazole begins after 3-5 days treatment. Even after 28 days application no significant rebound effects were seen after withdrawal from the medication. Omeprazole was clinically tested on several thousand patients. The daily doses of 20 mg to 60 mg in cases of duodenal ulcer led to healing rates of 60-100% after 14 days. In direct comparative studies omeprazole was superior in cases of duodenal ulcers to cimetidine and ranitidine. With regard to gastric ulcers identical successful results were seen with 20 mg omeprazole daily as with 2 X 150 mg ranitidine daily. Omeprazole was also superior to H2-blockers in the treatment of erosive reflux-oesophagitis. Results from long-term therapy with the exception of Zollinger-Ellison syndrome are not yet available. In the clinical studies, omeprazole proved to be well tolerated. Its definite place in the management of peptic ulcer disease, however, remains to clearly established.
奥美拉唑是一种取代苯并咪唑,能深刻且持久地抑制人体胃酸分泌。奥美拉唑的最大抑制作用在治疗3 - 5天后开始。即使应用28天后停药,也未见明显的反跳效应。奥美拉唑已在数千名患者身上进行了临床试验。十二指肠溃疡患者每日服用20毫克至60毫克,14天后愈合率达60 - 100%。在直接对比研究中,奥美拉唑治疗十二指肠溃疡的效果优于西咪替丁和雷尼替丁。对于胃溃疡,每日服用20毫克奥美拉唑与每日服用2次150毫克雷尼替丁的效果相同。在治疗糜烂性反流性食管炎方面,奥美拉唑也优于H2受体阻滞剂。除卓 - 艾综合征外,长期治疗的结果尚不可得。在临床研究中,奥美拉唑耐受性良好。然而,其在消化性溃疡疾病治疗中的明确地位仍有待明确确立。