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在降低胃酸度和抗分泌反应变异性方面,pH值反馈控制的雷尼替丁输注并不比固定剂量输注更有效。

pH-feedback controlled infusions of ranitidine are no more effective than fixed-dose infusions in reducing gastric acidity and variability in antisecretory responses.

作者信息

Wilder-Smith C H, Halter F, Häcki W, Merki H S

机构信息

Department of Medicine, University of Berne, Switzerland.

出版信息

Br J Clin Pharmacol. 1992 May;33(5):487-93. doi: 10.1111/j.1365-2125.1992.tb04075.x.

Abstract
  1. The antisecretory responses to pH-feedback controlled (maximum dose 800 mg 24 h-1) and fixed-dose (0.25 mg kg-1 h-1) continuous infusions of ranitidine were compared in a randomised, placebo-controlled, cross-over study in 10 healthy male volunteers. 2. To assess tolerance during repeated dosing with ranitidine, the same infusion regimens were given before and after 6 days oral dosing with ranitidine 300 mg four times daily. 3. With the pH-feedback controlled infusion of ranitidine the median % time (interquartile range) with pH greater than 4 in the 24 h period was 57% (45-76) before and 23% (17-34) after 6 days oral dosing (P less than 0.001). The respective values with fixed-dose infusion were 51% (38-63) and 26% (15-32) (P less than 0.002). 4. The median 24 h doses (interquartile range) of ranitidine given by feedback-controlled infusion before and after 6 days oral dosing were 675 mg (542-728) and 749 mg (709-760), respectively (P less than 0.01). The dose of ranitidine given by fixed-rate infusion was 423 mg (393-502) on both study days (P less than 0.001 vs feedback infusion). 5. Plasma gastrin concentrations remained slightly elevated after 6 days of oral ranitidine dosing, whereas pancreatic polypeptide plasma levels remained unchanged. 6. The antisecretory efficacy of infusions of ranitidine is significantly decreased by circadian stimuli and tolerance. Individually-adapted infusions of high doses of ranitidine were not superior to fixed-dose infusion of 0.25 mg kg-1 h-1 in overcoming this variability.
摘要
  1. 在一项针对10名健康男性志愿者的随机、安慰剂对照、交叉研究中,比较了雷尼替丁pH反馈控制(最大剂量800毫克/24小时)和固定剂量(0.25毫克/千克/小时)持续输注的抗分泌反应。2. 为评估雷尼替丁重复给药期间的耐受性,在每日4次口服300毫克雷尼替丁6天前后,给予相同的输注方案。3. 采用pH反馈控制输注雷尼替丁时,24小时内pH大于4的中位时间百分比(四分位间距)在口服给药6天前为57%(45 - 76),给药后为23%(17 - 34)(P小于0.001)。固定剂量输注时的相应值分别为51%(38 - 63)和26%(15 - 32)(P小于0.002)。4. 口服给药6天前后,通过反馈控制输注的雷尼替丁24小时中位剂量(四分位间距)分别为675毫克(542 - 728)和749毫克(709 - 760)(P小于0.01)。在两个研究日,固定速率输注的雷尼替丁剂量均为423毫克(393 - 502)(与反馈输注相比,P小于0.001)。5. 口服雷尼替丁6天后,血浆胃泌素浓度仍略有升高,而血浆胰多肽水平保持不变。6. 昼夜刺激和耐受性会显著降低雷尼替丁输注的抗分泌疗效。在克服这种变异性方面,个体化调整的高剂量雷尼替丁输注并不优于0.25毫克/千克/小时的固定剂量输注。

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Scand J Gastroenterol. 1984 May;19(3):429-32.

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