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Effect of a single oral dose of rabeprazole on nocturnal acid breakthrough and nocturnal alkaline amplitude

机译:单次口服雷贝拉唑对夜间酸突破和夜间碱性振幅的影响

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摘要

AIM: 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).METHODS: 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 h before and 24 h after the dose was given.RESULTS: 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).CONCLUSION: 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.
机译:目的:研究雷贝拉唑(RAB)对夜间酸突破(NAB)和夜间碱性振幅(NAKA)的影响,并将其与奥美拉唑(OME)和pan托拉唑(PAN)进行比较。方法:通过一项开放比较研究,对40名患者进行了研究。患有活动性消化性溃疡的患者被随机分配为接受单次口服剂量的三种PPI(质子泵抑制剂)之一。将其分为RAB组(10mg),OME组(20mg)和PAN组(40mg)。二十名健康志愿者被纳入对照组(不服用任何药物)。然后在给药前1小时和给药后24小时进行胃内pH监测。结果:在整个研究期间,均未发现可归因于RAB或OME和PAN给药的临床不良体征和症状。所有受试者均按照方案完成了研究。所有数据均通过计算机使用Student t检验或t'检验进行处理,然后进行协方差分析。 P <0.05被认为具有统计学意义。 RAB组的胃内pH值(1.84±0.55)显着高于OME组(1.15±0.31)或PAN组(1.10±0.30)(均P <0.01)。 RAB组NAKA的持续时间(4.65±1.22 h)比OME组(3.22±1.89 h)(P <0.05),PAN(3.15±1.92 h)(P <0.05)和NAKA组更长。也比健康对照组更长(P <0.01)。此外,与PAN(6.01±0.92)相比,RAB在NAKA上产生的pH值更高(6.41±0.45)(P <0.05)。结论:一次口服10 mg RAB可能会增加NAB的pH值并缩短NAB的pH。 NAB的维持时间,可能会增加NAKA的pH值,并延长NAKA的维持时间。

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