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一种维持静脉注射药物血浆水平恒定的近似的与模型无关的方法。

An approximate model-independent method to maintain constant plasma levels of intravenous drugs.

作者信息

Bailey J M

机构信息

Division of Cardiothoracic Anesthesia, Emory University School of Medicine, Atlanta, Georgia 30322.

出版信息

J Pharmacokinet Biopharm. 1991 Dec;19(6):635-45. doi: 10.1007/BF01080871.

DOI:10.1007/BF01080871
PMID:1815045
Abstract

To rapidly achieve and maintain constant plasma concentrations most intravenous drugs must be administered as an initial bolus followed by a combination of exponentially declining plus constant-rate infusions. In the clinical practice of anesthesia and critical care medicine this is often not practical without specialized equipment. In this paper a simpler approach of maintaining approximately constant plasma concentrations is developed using a loading dose with a two-stage infusion scheme (an initial rapid infusion reduced at a given time to a lower rate). Equations are developed for determining the rate of the infusions as well as the duration of the initial infusion by equating moments of the Laplace transform of the approximate infusion to the moments of the Laplace transform of an exact solution. This approach is independent of models and uses as parameters the moments of the curve relating the concentration following a single iv dose of unit magnitude as a function of time. The accuracy of this technique was assessed by computer simulation.

摘要

为了迅速达到并维持恒定的血浆浓度,大多数静脉注射药物必须先给予一次初始推注,随后进行指数衰减加恒速输注的联合给药方式。在麻醉和重症医学的临床实践中,如果没有专门的设备,这种方法往往不实用。本文提出了一种更简单的维持近似恒定血浆浓度的方法,即采用负荷剂量和两阶段输注方案(初始快速输注,在给定时间后降至较低速率)。通过使近似输注的拉普拉斯变换的矩与精确解的拉普拉斯变换的矩相等,推导出了确定输注速率以及初始输注持续时间的方程。这种方法独立于模型,并将单次静脉注射单位剂量后浓度随时间变化曲线的矩作为参数。通过计算机模拟评估了该技术的准确性。

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引用本文的文献

1
Rapid attainment of steady state plasma drug concentrations within precise limits.在精确限度内迅速达到稳态血浆药物浓度。
J Pharmacokinet Biopharm. 1998 Jun;26(3):319-28. doi: 10.1023/a:1023285426388.

本文引用的文献

1
Intravenous fentanyl kinetics.静脉注射芬太尼的动力学
Clin Pharmacol Ther. 1980 Jul;28(1):106-14. doi: 10.1038/clpt.1980.138.
2
A method for achieving rapidly steady-state blood concentrations of I.V. drugs.一种实现静脉注射药物快速稳态血药浓度的方法。
Br J Anaesth. 1981 Dec;53(12):1247-57. doi: 10.1093/bja/53.12.1247.
3
Automated gas chromatography for studies of midazolam pharmacokinetics.用于咪达唑仑药代动力学研究的自动气相色谱法。
Anesthesiology. 1981 Aug;55(2):176-9. doi: 10.1097/00000542-198108000-00014.
4
Continuous intravenous infusion and multicompartment accumulation.
Eur J Pharmacol. 1968 Oct;4(3):317-24. doi: 10.1016/0014-2999(68)90100-3.
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A safe method for rapidly achieving plasma concentration plateaus.一种快速达到血浆浓度平台期的安全方法。
Clin Pharmacol Ther. 1974 Oct;16(4):691-700. doi: 10.1002/cpt1974164691.
6
Computer-assisted continuous infusions of fentanyl during cardiac anesthesia: comparison with a manual method.心脏麻醉期间计算机辅助持续输注芬太尼:与手动方法的比较。
Anesthesiology. 1985 Jul;63(1):41-9. doi: 10.1097/00000542-198507000-00006.
7
Pharmacokinetics of fentanyl administered by computer-controlled infusion pump.
Anesthesiology. 1990 Dec;73(6):1091-102. doi: 10.1097/00000542-199012000-00005.
8
Pharmacokinetic model-driven infusion of fentanyl: assessment of accuracy.药代动力学模型驱动的芬太尼输注:准确性评估
Anesthesiology. 1990 Dec;73(6):1082-90. doi: 10.1097/00000542-199012000-00004.
9
General derivation of the ideal intravenous drug input required to achieve and maintain a constant plasma drug concentration. Theoretical application to lignocaine therapy.实现并维持恒定血浆药物浓度所需理想静脉药物输入的一般推导。利多卡因治疗的理论应用。
Eur J Clin Pharmacol. 1976;10(6):433-40. doi: 10.1007/BF00563080.
10
A linear recirculation model for drug disposition.一种药物处置的线性再循环模型。
J Pharmacokinet Biopharm. 1979 Feb;7(1):101-16. doi: 10.1007/BF01059445.