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依托度酸、阿司匹林与胃肠道微出血

Etodolac, aspirin, and gastrointestinal microbleeding.

作者信息

Arnold J D, Mullane J F, Hayden D M, March L, Hart K, Perdomo C A, Fencik M, Berger A E

出版信息

Clin Pharmacol Ther. 1984 May;35(5):716-21. doi: 10.1038/clpt.1984.100.

Abstract

The effects of etodolac, a new nonsteroidal anti-inflammatory drug, on gastrointestinal (GI) microbleeding were quantitatively assessed in two studies in healthy adult men. The first was a two-group, open-label, parallel comparison of etodolac, 600 mg/day, aspirin, 2600 mg/day, and placebo in 20 subjects; the second was a four-group, double-blind, parallel comparison of etodolac, 600, 800, and 1200 mg/day, aspirin, 2600 mg/day, and placebo in 41 subjects. Subjects in both studies received a single-blind placebo on days 1 through 7, either etodolac or aspirin on days 8 through 14, and a single-blind placebo on days 15 through 19. GI blood loss (milliliters per day) was estimated by the radiolabeled (51Cr) erythrocyte method and was based on daily radioactivity counts of stool specimens and regression-estimated daily blood radioactivity. Etodolac, 600 mg/day, induced no significant GI blood loss at any time during the experiments, nor was there significant blood loss after 800 and 1200 mg/day in experiment 2. Blood loss was noted after aspirin in both.

摘要

在两项针对健康成年男性的研究中,对新型非甾体抗炎药依托度酸对胃肠道微出血的影响进行了定量评估。第一项研究为开放标签、两组平行对照试验,纳入20名受试者,比较600毫克/天的依托度酸、2600毫克/天的阿司匹林及安慰剂;第二项研究为双盲、四组平行对照试验,纳入41名受试者,比较600、800和1200毫克/天的依托度酸、2600毫克/天的阿司匹林及安慰剂。两项研究的受试者在第1至7天接受单盲安慰剂,第8至14天接受依托度酸或阿司匹林,第15至19天接受单盲安慰剂。胃肠道失血量(每天毫升数)采用放射性标记(51Cr)红细胞法估算,基于粪便标本的每日放射性计数及回归估计的每日血液放射性。在实验期间,600毫克/天的依托度酸在任何时间均未引起显著胃肠道失血,在实验2中,800和1200毫克/天的依托度酸给药后也未出现显著失血。两项研究中阿司匹林给药后均出现失血。

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