Duval Justin D, Pang Jessica M, Boysen Søren R, Caulkett Nigel A
Department of Veterinary Clinical and Diagnostic Sciences, Faculty of Veterinary Medicine, University of Calgary, Calgary, Alberta, Canada.
Department of Clinical Sciences, Faculty of Veterinary Medicine, University of Montreal, Quebec, Canada.
J Am Assoc Lab Anim Sci. 2018 Jul 1;57(4):376-381. doi: 10.30802/AALAS-JAALAS-17-000164. Epub 2018 Jun 22.
Various anesthetic protocols are used in laboratory swine, each with specific advantages and disadvantages. Partial intravenous anesthetic techniques (PIVA) help minimize dose-dependent cardiopulmonary effects of inhalant drugs. The aim of this study was to determine the cardiopulmonary effects of a PIVA in laboratory swine. In a prospective, nonrandomized clinical study, 8 healthy juvenile Landrace-White pigs were premedicated with azaperone (0.20 ± 0.20 mg/kg IM), dexmedetomidine (0.02 ± 0.002 mg/kg IM), and alfaxalone (2.0 ± 0.20 mg/kg IM), and anesthesia was induced with intravenous alfaxalone. Anesthesia was maintained by using constant-rate infusion of dexmedetomidine (2 μg/kg/h) and alfaxalone (25 μg/kg/min) in combination with isoflurane. After the fraction of expired isoflurane was adjusted to 1.1% to 1.5%, respiratory rate, heart rate, systemic and pulmonary arterial pressure, central venous pressure, cardiac output, bispectral index, systemic vascular resistance, and arterial and mixed venous blood gases were recorded every 10 min for 60 min. Statistical analysis consisted of repeated-measures one-way ANOVA. Significant decreases occurred in heart rate, pulmonary mean arterial pressure, pulmonary diastolic pressure, partial pressure of arterial oxygen, partial pressure of venous oxygen; significant increases occurred in respiratory rate, minute volume index, diastolic arterial blood pressure, systemic vascular resistance, and arterial pH over time. We consider that the observed statistically significant cardiopulmonary changes were clinically important and that the PIVA protocol provided hemodynamic and respiratory stability for short-term anesthesia of laboratory swine.
实验室猪使用了各种麻醉方案,每种方案都有其特定的优缺点。部分静脉麻醉技术(PIVA)有助于将吸入性药物的剂量依赖性心肺效应降至最低。本研究的目的是确定PIVA对实验室猪的心肺效应。在一项前瞻性、非随机临床研究中,8只健康的幼年长白猪先用阿扎哌隆(0.20±0.20毫克/千克,肌肉注射)、右美托咪定(0.02±0.002毫克/千克,肌肉注射)和阿法沙龙(2.0±0.20毫克/千克,肌肉注射)进行预处理,然后用静脉注射阿法沙龙诱导麻醉。通过持续输注右美托咪定(2微克/千克/小时)和阿法沙龙(25微克/千克/分钟)并联合异氟烷维持麻醉。将呼出异氟烷分数调整至1.1%至1.5%后,每10分钟记录一次呼吸频率、心率、体循环和肺动脉压、中心静脉压、心输出量、脑电双频指数、体循环血管阻力以及动脉血和混合静脉血气,共记录60分钟。统计分析采用重复测量单向方差分析。随着时间的推移,心率、肺平均动脉压、肺舒张压、动脉血氧分压、静脉血氧分压显著下降;呼吸频率、分钟通气量指数、动脉舒张压、体循环血管阻力和动脉pH值显著升高。我们认为观察到的具有统计学意义的心肺变化具有临床重要性,并且PIVA方案为实验室猪的短期麻醉提供了血流动力学和呼吸稳定性。