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两剂右美托咪定联合丁丙诺啡用于犬的术前用药;与乙酰丙嗪和丁丙诺啡的比较。

Two doses of dexmedetomidine in combination with buprenorphine for premedication in dogs; a comparison with acepromazine and buprenorphine.

作者信息

Bell Andrew M, Auckburally Adam, Pawson Patricia, Scott E Marian, Flaherty Derek

机构信息

Anaesthesia Group, Institute of Comparative Medicine, Faculty of Veterinary Medicine, University of Glasgow, Glasgow, UK.

出版信息

Vet Anaesth Analg. 2011 Jan;38(1):15-23. doi: 10.1111/j.1467-2995.2010.00576.x.

Abstract

OBJECTIVE

To assess as premedicants, the sedative, cardiorespiratory and propofol-sparing effects in dogs of dexmedetomidine and buprenorphine compared to acepromazine and buprenorphine.

STUDY DESIGN

Prospective, randomised, blinded clinical study.

ANIMALS

Sixty healthy dogs (ASA grades I/II). Mean (SD) body mass 28.0 ± 9.1 kg, and mean age 3.4 ± 2.3 years.

METHODS

Dogs were allocated randomly to receive 15 μg kg(-1) buprenorphine combined with either 30 μg kg(-1) acepromazine (group 1), 62.5 μg m(-2) dexmedetomidine (group 2), or 125 μg m(-2) dexmedetomidine (group 3) intramuscularly. After 30 minutes, anaesthesia was induced using a propofol target controlled infusion. Heart rate, respiratory rate, and oscillometric arterial blood pressure were recorded prior to induction, at endotracheal intubation and at 3 and 5 minutes post-intubation. Induction quality and pre-induction sedation were scored on 4 point scales. Propofol target required for endotracheal intubation was recorded. Data were analysed using Chi-squared tests, Kruskal-Wallis, one way and general linear model ANOVA (p<0.05).

RESULTS

Age was significantly lower in group 1 (1.0 (1.0-3.8) years) than group 2 (5.0 (2.0-7.0) years), (median, (IQR)). There were no significant differences in sedation or quality of induction between groups. After premedication, heart rate was significantly lower and arterial blood pressures higher in groups 2 and 3 than group 1, but there was no significant difference between groups 2 and 3. Propofol targets were significantly lower in group 3 (1.5 (1.0-2.5) μg mL(-1) ) than group 1 (2.5 (2.0-3.0) μg mL(-1) ); no significant differences existed between group 2 (2.0 (1.5-2.5) μg mL(-1) ) and the other groups (median, (interquartile range)).

CONCLUSIONS AND CLINICAL RELEVANCE

When administered with buprenorphine, at these doses, dexmedetomidine had no advantages in terms of sedation and induction quality over acepromazine. Both doses of dexmedetomidine produced characteristic cardiovascular and respiratory effects of a similar magnitude.

摘要

目的

评估与乙酰丙嗪和丁丙诺啡相比,右美托咪定和丁丙诺啡作为术前用药在犬中的镇静、心肺和节省丙泊酚的效果。

研究设计

前瞻性、随机、双盲临床研究。

动物

60只健康犬(美国麻醉医师协会分级I/II级)。平均(标准差)体重28.0±9.1kg,平均年龄3.4±2.3岁。

方法

将犬随机分配接受15μg/kg丁丙诺啡联合30μg/kg乙酰丙嗪(第1组)、62.5μg/m²右美托咪定(第2组)或125μg/m²右美托咪定(第3组)肌肉注射。30分钟后,使用丙泊酚靶控输注诱导麻醉。在诱导前、气管插管时以及插管后3分钟和5分钟记录心率、呼吸频率和示波动脉血压。诱导质量和诱导前镇静用4分制评分。记录气管插管所需的丙泊酚靶浓度。数据采用卡方检验、Kruskal-Wallis检验、单因素和一般线性模型方差分析(p<0.05)。

结果

第1组(1.0(1.0 - 3.8)岁)的年龄显著低于第2组(5.0(2.0 - 7.0)岁)(中位数,(四分位间距))。各组之间在镇静或诱导质量方面无显著差异。术前用药后,第2组和第3组的心率显著低于第1组,动脉血压高于第1组,但第2组和第3组之间无显著差异。第3组(1.5(1.0 - 2.5)μg/mL)的丙泊酚靶浓度显著低于第1组(2.5(2.0 - 3.0)μg/mL);第2组(2.0(1.5 - 2.5)μg/mL)与其他组之间无显著差异(中位数,(四分位间距))。

结论及临床意义

在与丁丙诺啡联合使用时,在这些剂量下,右美托咪定在镇静和诱导质量方面并不优于乙酰丙嗪。两种剂量的右美托咪定产生的心血管和呼吸效应特征相似且程度相近。

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