首页> 外文期刊>Veterinary Anaesthesia and Analgesia >Two doses of dexmedetomidine in combination with buprenorphine for premedication in dogs; a comparison with acepromazine and buprenorphine.
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Two doses of dexmedetomidine in combination with buprenorphine for premedication in dogs; a comparison with acepromazine and buprenorphine.

机译:两剂右美托咪定联合丁丙诺啡用于犬的前药治疗;与醋丙嗪和丁丙诺啡的比较。

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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+or-9.1 kg, and mean age 3.4+or-2.3 years. Methods: Dogs were allocated randomly to receive 15 micro g kg-1 buprenorphine combined with either 30 micro g kg-1 acepromazine (group 1), 62.5 micro g m-2 dexmedetomidine (group 2), or 125 micro g 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) micro g mL-1) than group 1 (2.5 (2.0-3.0) micro g mL-1); no significant differences existed between group 2 (2.0 (1.5-2.5) micro g 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.
机译:目的:评估右美托咪定和丁丙诺啡与乙酰丙嗪和丁丙诺啡相比在犬中的镇静,心肺和丙泊酚的镇静作用。研究设计:前瞻性,随机,盲法临床研究。动物:六十只健康的狗(ASA I / II级)。平均(SD)体重28.0 +或-9.1公斤,平均年龄3.4 +或-2.3岁。方法:将狗随机分配以接受15 micro g kg -1 丁丙诺啡和30 micro g kg -1 醋丙嗪(第1组),62.5 micro gm 肌肉注射-2 右美托咪定(第2组)或125 micro gm -2 右美托咪定(第3组)。 30分钟后,使用异丙酚靶控输注进行麻醉。诱导前,气管内插管时以及插管后3和5分钟记录心率,呼吸率和示波动脉血压。归纳质量和归纳前镇静以4分制评分。记录气管插管所需的异丙酚靶标。使用卡方检验,Kruskal-Wallis,一种方法和一般线性模型ANOVA( p <0.05)来分析数据。结果:第1组(1.0(1.0-3.8)岁)的年龄明显低于第2组(5.0(2.0-7.0)岁)(中位数(IQR))。两组之间的镇静或诱导质量无明显差异。预防性用药后,第2组和第3组的心率显着降低,而动脉血压高于第1组,但第2组和第3组之间无显着差异。第3组的异丙酚靶点显着降低(1.5(1.0-2.5)micro g mL -1 )比第1组(2.5(2.0-3.0)micro g mL -1 );第2组(2.0(1.5-2.5)micro g mL -1 )与其他组(中位数,(四分位间距))之间没有显着差异。结论和临床意义:当与丁丙诺啡一起使用时,在这些剂量下,右美托咪定在镇静和诱导质量方面均不优于乙酰丙嗪。两种剂量的右美托咪定均产生相似程度的特征性心血管和呼吸作用。

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