Liao PenTing, Sinclair Melissa, Valverde Alexander, Mosley Cornelia, Chalmers Heather, Mackenzie Shawn, Hanna Brad
Department of Clinical Studies, Ontario Veterinary College, University of Guelph, Guelph, ON, Canada.
Department of Clinical Studies, Ontario Veterinary College, University of Guelph, Guelph, ON, Canada.
Vet Anaesth Analg. 2017 Sep;44(5):1016-1026. doi: 10.1016/j.vaa.2017.02.011. Epub 2017 Apr 29.
To compare propofol and alfaxalone, with or without midazolam, for induction of anesthesia in fentanyl-sedated dogs, and to assess recovery from total intravenous anesthesia (TIVA).
Prospective, incomplete, Latin-square study.
Ten dogs weighing 24.5 ± 3.1 kg (mean ± standard deviation).
Dogs were randomly assigned to four treatments: treatment P-M, propofol (1 mg kg) and midazolam (0.3 mg kg); treatment P-S, propofol and saline; treatment A-M, alfaxalone (0.5 mg kg) and midazolam; treatment A-S, alfaxalone and saline, administered intravenously (IV) 10 minutes after fentanyl (7 μg kg) IV. Additional propofol or alfaxalone were administered as necessary for endotracheal intubation. TIVA was maintained for 35-55 minutes by infusions of propofol or alfaxalone. Scores were assigned for quality of sedation, induction, extubation and recovery. The drug doses required for intubation and TIVA, times from sedation to end of TIVA, end anesthesia to extubation and to standing were recorded. Analysis included a general linear mixed model with post hoc analysis (p < 0.05).
Significant differences were detected in the quality of induction, better in A-M than A-S and P-S, and in P-M than P-S; in total intubation dose, lower in P-M (1.5 mg kg) than P-S (2.1 mg kg), and A-M (0.62 mg kg) than A-S (0.98 mg kg); and lower TIVA rate in P-M (268 μg kg minute) than P-S (310 μg kg minute). TIVA rate was similar in A-M and A-S (83 and 87 μg kg minute, respectively). Time to standing was longer after alfaxalone than propofol, but was not influenced by midazolam.
Addition of midazolam reduced the induction doses of propofol and alfaxalone and improved the quality of induction in fentanyl-sedated dogs. The dose rate of propofol for TIVA was decreased.
比较丙泊酚和阿法沙龙单独或联合咪达唑仑用于芬太尼镇静犬的麻醉诱导,并评估全静脉麻醉(TIVA)后的苏醒情况。
前瞻性、不完全拉丁方研究。
10只体重为24.5±3.1千克(均值±标准差)的犬。
将犬随机分为四种处理组:P-M组,丙泊酚(1毫克/千克)和咪达唑仑(0.3毫克/千克);P-S组,丙泊酚和生理盐水;A-M组,阿法沙龙(0.5毫克/千克)和咪达唑仑;A-S组,阿法沙龙和生理盐水,在静脉注射芬太尼(7微克/千克)10分钟后静脉注射。必要时追加丙泊酚或阿法沙龙以进行气管插管。通过输注丙泊酚或阿法沙龙维持TIVA 35 - 55分钟。对镇静、诱导、拔管和苏醒质量进行评分。记录插管和TIVA所需的药物剂量、从镇静到TIVA结束、麻醉结束到拔管以及到站立所需的时间。分析采用一般线性混合模型并进行事后分析(p<0.05)。
在诱导质量方面检测到显著差异,A-M组优于A-S组和P-S组,P-M组优于P-S组;在总插管剂量方面,P-M组(1.5毫克/千克)低于P-S组(2.1毫克/千克),A-M组(0.62毫克/千克)低于A-S组(0.98毫克/千克);P-M组的TIVA速率(268微克/千克·分钟)低于P-S组(310微克/千克·分钟)。A-M组和A-S组的TIVA速率相似(分别为83和87微克/千克·分钟)。阿法沙龙组后的站立时间比丙泊酚组长,但不受咪达唑仑影响。
添加咪达唑仑可降低丙泊酚和阿法沙龙在芬太尼镇静犬中的诱导剂量,并改善诱导质量。丙泊酚用于TIVA的剂量率降低。