Luo Jin-Yan, Niu Chun-Yan, Wang Xue-Qin, Zhu You-Ling, Gong Jun
Department of Gastroenterology, The Second Hospital of Xi'an Jiaotong University, Xi'an 710004, Shanxi Province, China.
World J Gastroenterol. 2003 Nov;9(11):2583-6. doi: 10.3748/wjg.v9.i11.2583.
To study the effect of rabeprazole (RAB) on nocturnal acid breakthrough (NAB) and nocturnal alkaline amplitude (NAKA) and to compare it with omeprazole (OME) and pantoprazole (PAN).
By an open comparative study, forty patients with active peptic ulcer were randomly assigned to receive one of the three PPIs (proton pump inhibitor) with a single oral dose. They were divided into RAB group (10 mg), OME group (20 mg) and PAN group (40 mg). Twenty healthy volunteers were enrolled to the control group (without taking any drug). Intragastric pH monitoring was then performed 1 hour before and 24 hours after the dose was given.
No clinically undesirable signs and symptoms possibly attributed to the administration of RAB or OME and PAN were recognizable throughout the study period. All subjects completed the study according to the protocol. All data were processed by a computer using the Student t test or t' test followed by an analysis of covariance. P<0.05 was considered to have statistical significance. The intragastric pH of NAB was significantly higher in RAB group (1.84+/-0.55) than in either OME group (1.15+/-0.31) or PAN group (1.10+/-0.30) (both P<0.01). RAB produced a longer sustaining time (4.65+/-1.22 h) on NAKA than OME (3.22+/-1.89 h) (P<0.05), PAN (3.15+/-1.92 h) (P<0.05), and the sustaining time of NAKA in RAB group was longer than that in the healthy control group (P<0.01) too. In addition, RAB produced a much higher pH on NAKA (6.41+/-0.45) in comparison with PAN (6.01+/-0.92) (P<0.05).
A single oral dose of 10 mg RAB may increase the pH of NAB and shorten the sustaining time of NAB, and it may increase the pH of NAKA as well as prolong the sustaining time of NAKA.
研究雷贝拉唑(RAB)对夜间酸突破(NAB)和夜间碱潮幅度(NAKA)的影响,并与奥美拉唑(OME)和泮托拉唑(PAN)进行比较。
采用开放对照研究,将40例活动性消化性溃疡患者随机分为三组,分别单次口服三种质子泵抑制剂(PPI)之一。分为RAB组(10毫克)、OME组(20毫克)和PAN组(40毫克)。选取20名健康志愿者作为对照组(不服用任何药物)。给药前1小时和给药后24小时进行胃内pH监测。
在整个研究期间,未发现可能归因于RAB、OME或PAN给药的临床不良体征和症状。所有受试者均按方案完成研究。所有数据通过计算机使用Student t检验或t'检验,随后进行协方差分析。P<0.05被认为具有统计学意义。RAB组NAB的胃内pH值(1.84±0.55)显著高于OME组(1.15±0.31)和PAN组(1.10±0.30)(均P<0.01)。RAB对NAKA的维持时间(4.65±1.22小时)长于OME(3.22±1.89小时)(P<0.05)、PAN(3.15±1.92小时)(P<0.05),且RAB组NAKA的维持时间也长于健康对照组(P<0.01)。此外,与PAN(6.01±0.92)相比,RAB在NAKA时产生的pH值更高(6.41±0.45)(P<0.05)。
单次口服10毫克RAB可能会提高NAB的pH值并缩短NAB的维持时间,同时可能会提高NAKA的pH值并延长NAKA的维持时间。