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阿替美唑作为犬咪达唑仑拮抗剂的临床疗效。

The clinical effectiveness of atipamezole as a medetomidine antagonist in the dog.

作者信息

Vähä-Vahe A T

机构信息

Farmos Group Ltd., Research Center, Turku, Finland.

出版信息

J Vet Pharmacol Ther. 1990 Jun;13(2):198-205. doi: 10.1111/j.1365-2885.1990.tb00769.x.

Abstract

The efficacy of atipamezole, a recently introduced alpha 2-adrenoceptor antagonist, in reversing medetomidine-induced effects in dogs was investigated in a clinical study. Dogs from eight Finnish small-animal hospitals were sedated with a 40-microgram/kg dose of the alpha 2-agonist medetomidine i.m. In the first part of the study (n = 319), a randomized, double-blind design with respect to the dose of atipamezole (0, 80, 160 and 240 micrograms/kg i.m.) was used. In a separate study (n = 358), which was an open trial, the selected dose of atipamezole was 200 micrograms/kg i.m. Atipamezole at dose rates of 80-240 micrograms/kg rapidly and effectively reversed medetomidine-induced deep sedation-analgesia, recumbency and bradycardia. The median arousal time after atipamezole was 3-5 min, and walking time was 6-10 min compared to greater than 30 min for both effects after placebo. Heart rate also increased in a dose-related manner after atipamezole administration. The investigators' overall evaluation of the ability of atipamezole to reverse the effects of medetomidine was 'good' in 90%, and 'moderate' in 9% of cases. Relapse into sedation was reported in three individual cases. Side-effects were minimal. It is concluded that at doses four- to sixfold the medetomidine dose, atipamezole is a highly effective and safe agent in reversing medetomidine-induced sedation-analgesia, recumbency and bradycardia in dogs in veterinary practice.

摘要

在一项临床研究中,对最近引入的α2-肾上腺素能受体拮抗剂阿替美唑逆转美托咪定对犬类的诱导作用的疗效进行了研究。来自芬兰八家小动物医院的犬只通过肌肉注射40微克/千克剂量的α2-激动剂美托咪定进行镇静。在研究的第一部分(n = 319)中,采用了关于阿替美唑剂量(0、80、160和240微克/千克肌肉注射)的随机双盲设计。在另一项单独的开放性研究(n = 358)中,选择的阿替美唑剂量为200微克/千克肌肉注射。剂量为80 - 240微克/千克的阿替美唑能迅速有效地逆转美托咪定诱导的深度镇静镇痛、卧姿和心动过缓。与安慰剂后两种效应均大于30分钟相比,阿替美唑后的中位苏醒时间为3 - 5分钟,行走时间为6 - 10分钟。给药后心率也呈剂量相关增加。研究者对阿替美唑逆转美托咪定作用能力的总体评价在90%的病例中为“良好”,在9%的病例中为“中等”。有三例个体报告出现镇静复发。副作用极小。结论是,在美托咪定剂量的四至六倍剂量下,阿替美唑在兽医实践中是逆转美托咪定诱导的犬类镇静镇痛、卧姿和心动过缓的高效安全药物。

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