» Articles » PMID: 30255401

Population Pharmacokinetic Modelling for Estimation of Remifentanil Metabolic-Ratio Using Non-steady-State Concentrations Under Rapidly Adaptive Dosing

Overview
Journal Pharm Res
Specialties Pharmacology
Pharmacy
Date 2018 Sep 27
PMID 30255401
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: To predict steady-state metabolite-to-drug concentration ratio (metabolic ratio) for analgesic drug remifentanil, using sparse non-steady-state data from patients with normal or impaired renal function during individualised, highly variable and rapidly adaptive intravenous infusion.

Methods: A three-compartment joint parent-metabolite population pharmacokinetic model was developed using concentrations of remifentanil and its metabolite remifentanil acid from two trials. Renal function was included as an important mechanistic covariate. To address the large covariate effect and highly individualised and rapidly adaptive dosing, standardised visual predictive check was conducted on the observations and individualised visual predictive check was conducted on metabolic ratio estimates. The model was used to simulate metabolic ratio distribution in patients with various renal functions.

Results: The model, including its covariate structure, adequately described the data. The predictive checks allowed informative model evaluation. The predicted median (10th - 90th percentile) of remifentanil metabolic ratio was 12.5 (2.4-58.2) for patients with normal or mildly impaired renal function, or 54.3 (12.8-218.4) for patients with moderately or severely impaired renal function.

Conclusions: The methodologies applied here allowed robust estimation of steady-state parameters using non-steady-state sparse data under highly variable adaptive dosing.

References
1.
Dershwitz M, Hoke J, Rosow C, Michalowski P, Connors P, Muir K . Pharmacokinetics and pharmacodynamics of remifentanil in volunteer subjects with severe liver disease. Anesthesiology. 1996; 84(4):812-20. DOI: 10.1097/00000542-199604000-00008. View

2.
Bender J, van den Elshout J, Selinger K, Broeders G, Dankers J, van der Heiden C . Determination of remifentanil in human heparinised whole blood by tandem mass spectrometry with short-column separation. J Pharm Biomed Anal. 2000; 21(3):559-67. DOI: 10.1016/s0731-7085(99)00151-x. View

3.
Hoke J, Shlugman D, Dershwitz M, Michalowski P, Connors P, Martel D . Pharmacokinetics and pharmacodynamics of remifentanil in persons with renal failure compared with healthy volunteers. Anesthesiology. 1997; 87(3):533-41. DOI: 10.1097/00000542-199709000-00012. View

4.
Breen D, Wilmer A, Bodenham A, Bach V, Bonde J, Kessler P . Offset of pharmacodynamic effects and safety of remifentanil in intensive care unit patients with various degrees of renal impairment. Crit Care. 2004; 8(1):R21-30. PMC: 420060. DOI: 10.1186/cc2399. View

5.
Frame B, Miller R, Lalonde R . Evaluation of mixture modeling with count data using NONMEM. J Pharmacokinet Pharmacodyn. 2003; 30(3):167-83. DOI: 10.1023/a:1025564409649. View