Pettifer G, Dyson D, McDonell W
Department of Clinical Studies, Ontario Veterinary College, University of Guelph.
Can J Vet Res. 1997 Jul;61(3):221-6.
Repeat determinations of the arrhythmogenic dose of epinephrine (ADE) were made over two 6 h periods on 2 separate days during halothane and isoflurane anesthesia. Each of 6 dogs underwent 4 trials (2 halothane and 2 isoflurane). During each trial, the ADE was determined at baseline, 3 and 6 h. Epinephrine was infused for 3.0 min at increasing dose rates (2.5, 5.0, 10.0 and 20.0 mg/kg/min) until the arrhythmia criterion (4 or more intermittent or continuous premature ventricular contractions) was reached. The inter-infusion interval was 20 min. There were no significant differences in the measured cardiovascular parameters (SBP, DBP, MBP, and HR), arterial blood gases, or acid-base status prior to each determination during a single trial. The cardiovascular responses to epinephrine infusion were not significantly different between inhalants or determinations. The range of the ADE determined over both trials during isoflurane anesthesia was 30.12 +/- 12.21 micrograms/kg to 50.83 +/- 9.17 micrograms/kg. The baseline ADE during Day 1 of halothane anesthesia (6.70 +/- 1.36 micrograms/kg) was significantly greater than ADE determinations at 3 (4.65 +/- 0.88 micrograms/kg) and 6 h (4.61 +/- 0.87 micrograms/kg). The reduction in the ADE over time during day 2 of halothane anesthesia was not statistically significant (P = 0.0669). These results suggest that during halothane anesthesia, the ADE is not repeatable over time, and they may influence our interpretation of the results of investigations that measure alterations in the ADE due to pharmacological manipulations without repeated control ADE determinations.
在氟烷和异氟烷麻醉期间,于两个不同日期的两个6小时时间段内重复测定肾上腺素致心律失常剂量(ADE)。6只犬每只进行4次试验(2次氟烷试验和2次异氟烷试验)。在每次试验期间,于基线、3小时和6小时测定ADE。以递增的剂量率(2.5、5.0、10.0和20.0毫克/千克/分钟)输注肾上腺素3.0分钟,直至达到心律失常标准(4次或更多次间歇性或持续性室性早搏)。输注间隔为20分钟。在单次试验的每次测定之前,所测量的心血管参数(收缩压、舒张压、平均动脉压和心率)、动脉血气或酸碱状态均无显著差异。吸入麻醉剂之间或各次测定之间,对肾上腺素输注的心血管反应无显著差异。异氟烷麻醉期间两次试验所测定的ADE范围为30.12±12.21微克/千克至50.83±9.17微克/千克。氟烷麻醉第1天的基线ADE(6.70±1.36微克/千克)显著高于3小时(4.65±0.88微克/千克)和6小时(4.61±0.87微克/千克)时的ADE测定值。氟烷麻醉第2天期间ADE随时间的降低无统计学意义(P = 0.0669)。这些结果表明,在氟烷麻醉期间,ADE随时间不可重复,这可能会影响我们对那些在未重复对照ADE测定的情况下测量由于药理学操作导致的ADE变化的研究结果的解释。