Kapila A, Glass P S, Jacobs J R, Muir K T, Hermann D J, Shiraishi M, Howell S, Smith R L
Department of Anesthesia, Duke University Medical Center, Durham, North Carolina 27710, USA.
Anesthesiology. 1995 Nov;83(5):968-75. doi: 10.1097/00000542-199511000-00009.
The context-sensitive half-time, rather than the terminal elimination half-life, has been proposed as a more clinically relevant measure of decreasing drug concentration after a constant infusion of a given duration. The context-sensitive half-time is derived from computer modelling using known pharmacokinetic parameters. The modelled context-sensitive half-time for a 3-h infusion of alfentanil is 50-55 min and is 3 min for remifentanil. The terminal elimination half-life is 111 min for alfentanil and 12-30 min for remifentanil. It has not been tested whether the modelled context-sensitive half-time reflects the true time for a 50% decrease in drug concentration or drug effect.
Thirty volunteers received a 3-h infusion of remifentanil or alfentanil at equieffective concentrations. Depression of minute ventilation to 7.5% ETCO2 was used as a measure of drug effect. Minute ventilation response was measured, and blood samples for drug concentration were taken during and after drug infusion. The recovery of minute ventilation (drug effect) and decrease in blood drug concentration was plotted, and the time for a 50% change was determined.
The measured pharmacokinetic context-sensitive half-time for remifentanil after a 3-h infusion was 3.2 +/- 0.9 min, and its pharmacodynamic offset was 5.4 +/- 1.8 min. Alfentanil's measured pharmacokinetic context-sensitive half-time was 47.3 +/- 12 min, and its pharmacodynamic offset was 54.0 +/- 48 min. The terminal elimination half-life modelled from the volunteers was 11.8 +/- 5.1 min for remifentanil and 76.5 +/- 12.6 min for alfentanil.
The measured context-sensitive half-times were in close agreement with the context-sensitive half-times previously modelled for these drugs. The results of this study confirm the value of the context-sensitive half-time in describing drug offset compared to the terminal elimination half-life.
对于给定持续时间的持续输注后药物浓度下降情况,有人提出用上下文敏感半衰期而非终末消除半衰期作为更具临床相关性的指标。上下文敏感半衰期是通过使用已知药代动力学参数的计算机建模得出的。阿芬太尼输注3小时的建模上下文敏感半衰期为50 - 55分钟,瑞芬太尼为3分钟。阿芬太尼的终末消除半衰期为111分钟,瑞芬太尼为12 - 30分钟。尚未测试建模的上下文敏感半衰期是否反映药物浓度或药物效应降低50%的真实时间。
30名志愿者接受了等效应浓度的瑞芬太尼或阿芬太尼3小时输注。将分钟通气量降低至7.5%呼气末二氧化碳分压作为药物效应的指标。测量分钟通气反应,并在药物输注期间及之后采集血样以测定药物浓度。绘制分钟通气量(药物效应)的恢复情况和血药浓度的下降情况,并确定变化50%的时间。
瑞芬太尼输注3小时后测得的药代动力学上下文敏感半衰期为3.2±0.9分钟,其药效学消退时间为5.4±1.8分钟。阿芬太尼测得的药代动力学上下文敏感半衰期为47.3±12分钟,其药效学消退时间为54.0±48分钟。根据志愿者建模得出的瑞芬太尼终末消除半衰期为11.8±5.1分钟,阿芬太尼为76.5±12.6分钟。
测得的上下文敏感半衰期与先前针对这些药物建模得到的上下文敏感半衰期密切一致。本研究结果证实了与终末消除半衰期相比,上下文敏感半衰期在描述药物消退方面的价值。