Metz D C, Amer F, Hunt B, Vakily M, Kukulka M J, Samra N
University of Pennsylvania Health Sciences, Philadelphia, 19004, USA.
Aliment Pharmacol Ther. 2006 Apr 1;23(7):985-95. doi: 10.1111/j.1365-2036.2006.02850.x.
Orally and intravenously administered proton pump inhibitors have been shown to reduce rebleeding rates, surgery and transfusion requirement.
To compare lansoprazole intravenous and orally disintegrating tablet (Prevacid SoluTab) regimens with a pantoprazole intravenously administered regimen in sustaining intragastric pH >6.0.
Two similarly designed three-way, randomized crossover studies each enrolled 36 Helicobacter pylori-negative healthy volunteers. Study 1 regimens included intravenously administered bolus followed by 24-h continuous infusion (lansoprazole 90 mg, 6 mg/h; lansoprazole 120 mg, 6 mg/h; pantoprazole 80 mg, 8 mg/h). Study 2 regimens included intravenous bolus followed by lansoprazole orally disintegrating tablet or intravenous continuous infusion for 24 h (lansoprazole 90 mg, lansoprazole orally disintegrating tablet 60 mg every 6 h; lansoprazole 120 mg, 9 mg/h; pantoprazole 80 mg, 8 mg/h). Percentage of time pH >6.0 was assessed with 24-h intragastric pH monitoring.
All regimens produced comparable gastric acid suppression. In both studies, regimens superior to pantoprazole included lansoprazole 90 mg, 6-mg/h; lansoprazole 90 mg, lansoprazole orally disintegrating tablet 60 mg q.d.s. and lansoprazole 120 mg, 9 mg/h (P < or = 0.013). The lansoprazole 120-mg, 6-mg/h regimen (P = 0.082) was not superior to pantoprazole in percentage of time intragastric pH >6.0. Mild reaction at the intravenous injection site was the most frequently reported adverse event.
The intravenous bolus and continuously infused lansoprazole or intravenous bolus and intermittent lansoprazole orally disintegrating tablet regimens are as effective as intravenous pantoprazole in sustaining intragastric pH >6.0.
口服和静脉注射质子泵抑制剂已被证明可降低再出血率、手术需求和输血需求。
比较兰索拉唑静脉注射和口腔崩解片(耐信速溶片)方案与泮托拉唑静脉注射方案维持胃内pH>6.0的效果。
两项设计相似的三向随机交叉研究各纳入36名幽门螺杆菌阴性的健康志愿者。研究1的方案包括静脉推注后24小时持续输注(兰索拉唑90毫克,6毫克/小时;兰索拉唑120毫克,6毫克/小时;泮托拉唑80毫克,8毫克/小时)。研究2的方案包括静脉推注后口服兰索拉唑口腔崩解片或静脉持续输注24小时(兰索拉唑90毫克,兰索拉唑口腔崩解片60毫克,每6小时一次;兰索拉唑120毫克,9毫克/小时;泮托拉唑80毫克,8毫克/小时)。通过24小时胃内pH监测评估pH>6.0的时间百分比。
所有方案产生的胃酸抑制效果相当。在两项研究中,优于泮托拉唑的方案包括兰索拉唑90毫克,6毫克/小时;兰索拉唑90毫克,兰索拉唑口腔崩解片60毫克,每日四次;以及兰索拉唑120毫克,9毫克/小时(P≤0.013)。兰索拉唑120毫克,6毫克/小时方案在胃内pH>6.0的时间百分比方面并不优于泮托拉唑(P = 0.082)。静脉注射部位的轻度反应是最常报告的不良事件。
静脉推注并持续输注兰索拉唑或静脉推注并间歇性口服兰索拉唑口腔崩解片方案在维持胃内pH>6.0方面与静脉注射泮托拉唑一样有效。