Spencer C M, Faulds D
Adis International Limited, Auckland, New Zealand.
Drugs. 1994 Sep;48(3):404-30. doi: 10.2165/00003495-199448030-00007.
Lansoprazole is a benzimidazole derivative that effectively decreases gastric acid secretion, regardless of the primary stimulus, via inhibition of gastric H+,K(+)-adenosine triphosphatase (ATPase). It provides effective symptom relief and healing of peptic ulcer and reflux oesophagitis after 4 to 8 weeks of therapy and appears to prevent recurrence of lesions when administered as maintenance therapy. When administered at therapeutic dosages, lansoprazole produced higher healing rates than ranitidine or famotidine in patients with duodenal and gastric ulcers. Lansoprazole heals duodenal ulcers more rapidly than ranitidine or famotidine. Relief of ulcer symptoms in lansoprazole recipients is at least equivalent to, and tends to be more rapid than, that in patients receiving histamine H2-receptor antagonists. In comparisons with omeprazole 20 mg/day, lansoprazole 30 mg/day produced duodenal ulcer healing more rapidly and reduced ulcer pain to a greater extent at 2 weeks, but overall healing rates were similar after 4 weeks of therapy. At therapeutic dosages, lansoprazole produces superior healing and symptom relief of reflux oesophagitis in comparison with ranitidine, and it tends to relieve heartburn more effectively than omeprazole, although both agents produce equivalent healing. Healing of peptic ulcers or reflux oesophagitis refractory to histamine H2-receptor antagonists occurs after 8 weeks in the majority of patients treated with lansoprazole, and lansoprazole and omeprazole demonstrate similar efficacy in patients with refractory peptic ulcers. In patients with Zollinger-Ellison syndrome, lansoprazole effectively controls mean basal gastric acid output. Lansoprazole is generally well tolerated in clinical trials. The incidence of adverse effects is similar to that of omeprazole, ranitidine and famotidine in comparative studies. Combination therapy with lansoprazole and antibacterial agents such as amoxicillin, tinidazole, roxithromycin and/or metronidazole appears to eradicate Helicobacter pylori in 22 to 80% of patients with this organism. Limited data also suggest that lansoprazole may have superior activity against H. pylori in comparison with omeprazole, although the clinical relevance of this preliminary finding requires further confirmation. Thus, lansoprazole may be considered as alternative to existing antisecretory agents available for the treatment of acid-related disorders, particularly because it may provide more rapid healing and relief of symptoms.
兰索拉唑是一种苯并咪唑衍生物,它通过抑制胃H⁺,K⁺-腺苷三磷酸酶(ATP酶),有效地减少胃酸分泌,而不论其主要刺激因素如何。在治疗4至8周后,它能有效缓解症状并治愈消化性溃疡和反流性食管炎,并且在作为维持治疗给药时似乎能预防病变复发。在十二指肠溃疡和胃溃疡患者中,以治疗剂量给药时,兰索拉唑产生的愈合率高于雷尼替丁或法莫替丁。兰索拉唑治愈十二指肠溃疡的速度比雷尼替丁或法莫替丁更快。接受兰索拉唑治疗的患者溃疡症状的缓解至少与接受组胺H₂受体拮抗剂治疗的患者相当,并且往往更快。与每天20毫克奥美拉唑相比,每天30毫克兰索拉唑能更快地治愈十二指肠溃疡,并且在2周时能更大程度地减轻溃疡疼痛,但在治疗4周后总体愈合率相似。在治疗剂量下,与雷尼替丁相比,兰索拉唑能更好地治愈反流性食管炎并缓解症状,并且它缓解烧心的效果往往比奥美拉唑更有效,尽管两种药物的愈合效果相当。在大多数接受兰索拉唑治疗的患者中,8周后组胺H₂受体拮抗剂难治性消化性溃疡或反流性食管炎会愈合,并且兰索拉唑和奥美拉唑在难治性消化性溃疡患者中显示出相似的疗效。在卓-艾综合征患者中,兰索拉唑能有效控制平均基础胃酸分泌量。在临床试验中,兰索拉唑一般耐受性良好。在比较研究中,不良反应的发生率与奥美拉唑、雷尼替丁和法莫替丁相似。兰索拉唑与阿莫西林、替硝唑、罗红霉素和/或甲硝唑等抗菌药物联合治疗似乎能使22%至80%感染这种细菌的患者根除幽门螺杆菌。有限的数据还表明,与奥美拉唑相比,兰索拉唑对幽门螺杆菌可能具有更强的活性,尽管这一初步发现的临床相关性需要进一步证实。因此,兰索拉唑可被视为治疗酸相关疾病的现有抗分泌药物的替代品,特别是因为它可能能更快地促进愈合并缓解症状。