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Sedative and cardiopulmonary effects of acepromazine, midazolam, butorphanol, acepromazine-butorphanol and midazolam-butorphanol on propofol anaesthesia in goats

机译:乙酰丙嗪,咪达唑仑,布托啡诺,乙酰丙嗪 - 布托啡诺和咪达唑仑 - 布托啡诺对山羊异丙酚麻醉的镇静和心肺作用

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摘要

The sedative, propofol-sparing and cardiopulmonary effects of acepromazine, midazolam, butorphanol and combinations of butorphanol with acepromazine or midazolam in goats were evaluated. Six healthy Boer - Indigenous African crossbreed goats were by randomised cross-over designated to 6 groups: Group SAL that received saline, Group ACE that received acepromazine, Group MID that received midazolam, Group BUT that received butorphanol, Group ACEBUT that received acepromazine and butorphanol and Group MIDBUT that received midazolam and butorphanol as premedication agents intramuscularly on different occasions at least 3 weeks apart. The degree of sedation was assessed 20 minutes after administration of the premedication agents. Thirty minutes after premedication, the dose of propofol required for induction of anaesthesia adequate to allow placement of an endotracheal tube was determined. Cardiovascular, respiratory and arterial blood-gas parameters were assessed up to 30 minutes after induction of general anaesthesia. Acepromazine and midazolam produced significant sedation when administered alone, but premedication regimens incorporating butorphanol produced inconsistent results. The dose of propofol required for induction of anaesthesia was significantly reduced in goats that received midazolam alone, or midazolam combined with either acepromazine or butorphanol. The quality of induction of anaesthesia was good in all groups, including the control group. Cardiovascular, respiratory and blood-gas parameters were within normal limits in all groups and not significantly different between or within all groups. In conclusion: sedation with midazolam alone, or midazolam combined with either acepromazine or butorphanol significantly reduces the induction dose of propofol with minimal cardiopulmonary effects in goats.
机译:评估了乙酰丙嗪,咪达唑仑,丁吗啡醇的镇静,保留异丙酚和心肺作用以及丁烷啡醇与乙酰丙嗪或咪达唑仑的组合在山羊中的作用。将六只健康的布尔人-非洲土著杂种山羊随机分为6组:SAL组接受生理盐水,ACE组接受乙酰丙嗪,MID组接受咪达唑仑,BUT组接受butorphanol,ACEBUT组接受乙酰丙嗪和butorphanol。 MIDBUT组在不同情况下至少间隔3周,在不同情况下肌肉注射咪达唑仑和丁啡诺尔作为前药。在施用前药后20分钟评估镇静程度。在用药前三十分钟,确定足以引起气管插管的麻醉诱导所需的异丙酚剂量。全身麻醉诱导后30分钟内评估心血管,呼吸和动脉血气参数。单独使用时,乙酰丙嗪和咪达唑仑会产生明显的镇静作用,但结合丁苯啡诺的前药治疗方案却产生不一致的结果。在单独接受咪达唑仑或咪达唑仑与乙酰丙嗪或丁啡诺联用的山羊中,诱导麻醉所需的异丙酚剂量显着降低。在包括对照组在内的所有组中,麻醉诱导的质量均良好。在所有组中,心血管,呼吸和血气参数均在正常范围内,并且在所有组之间或之内没有显着差异。结论:在山羊中,单独使用咪达唑仑或咪达唑仑与醋丙嗪或布托啡诺合用镇静剂可显着降低异丙酚的诱导剂量,对心肺的影响最小。

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