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口服环拉马多治疗术后疼痛。

Oral ciramadol in the treatment of postoperative pain.

作者信息

Lasagna L, Calimlim J F

出版信息

Clin Pharmacol Ther. 1985 Aug;38(2):176-82. doi: 10.1038/clpt.1985.155.

Abstract

The efficacy and safety of single oral 15, 30, and 60 mg doses of ciramadol, an investigational agonist/antagonist analgesic, were studied in a postoperative pain model and compared with aspirin, 325 and 650 mg. Two visual analog pain assessment scales were also compared. Results showed that a pain relief score of moderate or better was reported at some time during the 6-hour observation period by 76% of the patients who took 15 mg ciramadol, by 60% of those who took 30 mg ciramadol, by 59% of those who took 60 mg ciramadol, and by 38% and 92% of the patients who took the low and high doses of aspirin, respectively. From 1 to 4 hours after drug dosing, 15 mg ciramadol generally produced higher scores, indicative of greater pain relief, on the three pain intensity efficacy scales used (verbal, linear analog, and curvilinear analog) than did the other two ciramadol doses, but these differences were generally not significant. The differences between 15 mg ciramadol and 650 mg aspirin were generally not significant, although the higher aspirin dose had some advantages over 15 mg ciramadol. The most frequently reported adverse effect was dizziness/vertigo in 22% of patients taking 60 mg ciramadol, in 17% of those taking 30 mg ciramadol, in 13% of those taking 15 mg ciramadol, in 4% of those taking high aspirin doses, and in none of those who received the low aspirin doses. The correlation coefficient for the linear and curvilinear pain analog intensity scales was 0.955, indicating a highly significant correlation (P less than 0.001).

摘要

在术后疼痛模型中研究了单次口服15毫克、30毫克和60毫克剂量的环拉马朵(一种研究中的激动剂/拮抗剂镇痛药)的疗效和安全性,并与325毫克和650毫克的阿司匹林进行了比较。还比较了两种视觉模拟疼痛评估量表。结果显示,在6小时观察期内的某个时间,服用15毫克环拉马朵的患者中有76%报告疼痛缓解评分中等或更好,服用30毫克环拉马朵的患者中有60%,服用60毫克环拉马朵的患者中有59%,服用低剂量和高剂量阿司匹林的患者分别有38%和92%。给药后1至4小时,在使用的三种疼痛强度疗效量表(言语、线性模拟和曲线模拟)上,15毫克环拉马朵通常比其他两种环拉马朵剂量产生更高的评分,表明疼痛缓解更大,但这些差异通常不显著。15毫克环拉马朵与650毫克阿司匹林之间的差异通常不显著,尽管较高剂量的阿司匹林比15毫克环拉马朵有一些优势。最常报告的不良反应是头晕/眩晕,服用60毫克环拉马朵的患者中有22%出现,服用30毫克环拉马朵的患者中有17%,服用15毫克环拉马朵的患者中有13%,服用高剂量阿司匹林的患者中有4%,而服用低剂量阿司匹林的患者中无一出现。线性和曲线疼痛模拟强度量表的相关系数为0.955,表明相关性非常显著(P小于0.001)。

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