Do distribution volumes and clearances relate to tissue volumes and blood flows? A computer simulation
© Hendrickx et al; licensee BioMed Central Ltd. 2006
Received: 03 February 2006
Accepted: 13 June 2006
Published: 13 June 2006
Kinetics of inhaled agents are often described by physiological models. However, many pharmacokinetic concepts, such as context-sensitive half-times, have been developed for drugs described by classical compartmental models. We derived classical compartmental models that describe the course of the alveolar concentrations (FA) generated by the physiological uptake and distribution models used by the Gas Man® program, and describe how distribution volumes and clearances relate to tissue volumes and blood flows.
Gas Man® was used to generate FA vs. time curves during the wash-in and wash-out period of 115 min each with a high fresh gas flow (8 L.min-1), a constant alveolar minute ventilation (4 L.min-1), and a constant inspired concentration (FI) of halothane (0.75%), isoflurane (1.15%), sevoflurane (2%), or desflurane (6%). With each of these FI, simulations were ran for a 70 kg patient with 5 different cardiac outputs (CO) (2, 3, 5, 8 and 10 L.min-1) and for 5 patients with different weights (40, 55, 70, 85, and 100 kg) but the same CO (5 L.min-1). Two and three compartmental models were fitted to FA of the individual 9 runs using NONMEM. After testing for parsimony, goodness of fit was evaluated using median prediction error (MDPE) and median absolute prediction error (MDAPE). The model was tested prospectively for a virtual 62 kg patient with a cardiac output of 4.5 L.min-1 for three different durations (wash-in and wash-out period of 10, 60, and 180 min each) with an FI of 1.5% halothane, 1.5% isoflurane, sevoflurane 4%, or desflurane 12%.
A three-compartment model fitted the data best (MDPE = 0% and MDAPE ≤ 0.074%) and performed equally well when tested prospectively (MDPE ≤ 0.51% and MDAPE ≤ 1.51%). The relationship between CO and body weight and the distribution volumes and clearances is complex.
The kinetics of anesthetic gases can be adequately described e by a mammilary compartmental model. Therefore, concepts that are traditionally thought of as being applicable to the kinetics of intravenous agents can be equally well applied to anesthetic gases. Distribution volumes and clearances cannot be equated to tissue volumes and blood flows respectively.
Like intravenous anesthetics, inhaled anesthetic agents can and are being safely administered without the knowledge of any pharmacokinetic model. In addition, the MAC and MAC awake concept link the end-expired concentrations (FA) with the clinically two most relevant endpoints, immobility and unconsciousness. Kinetic models can nevertheless be useful. Models are used to explain differences in wash-in and wash-out characteristics of different agents that may be relevant to clinical practice. Uptake models have also been used to try to predict the relationship between fresh gas flow, and delivered, inspired (FI), and end-expired concentrations of anesthetic agents in the commonly used circle breathing system . Once a kinetic model has been developed, it can be linked to clinically relevant endpoints (immobility and unconsciousness) by incorporating an effect site compartment.
Physiological models are appealing because they can be understood in terms of anatomy, physiology, and physics. The kinetics of inhaled agents are commonly described using physiological modeling because of the availability of values for tissue partition coefficients, tissue volumes and organ blood flows. Yet many assumptions underlie these models, such as the absence of an arterial-end-expired gradient or the assumption that uptake and distribution in an organ is uniform and instantaneous as implicitly assumed by flow limited uptake and the use of a single value for tissue partition coefficients . In addition, it is mathematically impossible to accurately fit all these parameters to "uptake" as it is clinically available in the operating room: the product of inspired concentration (FI) and ventilation minus the product of the end-expired concentration (FA) and ventilation. A parsimonious empirical polyexponential model ("classical compartmental modeling") similar to that used to describe the course of the concentration over time of intravenous agents may be better suited to analyze the partial pressure (or infusion rate) of potent inhaled anesthetics over time [3–5]. The first goal of this manuscript is to examine whether the kinetics of four different anesthetic agents generated by a physiological uptake model (used by the Gas Man® program, Med Man Simulations, Inc., Chestnut Hill, MA) can be equally well described by a mammilary compartmental model (derived using non-linear mixed effect modeling or NONMEM) . If so, concepts applied to intravenous agents, like the context-sensitive half time, would also be applicable to inhaled agents. The derived compartmental model will be prospectively tested against the physiological model used by the Gas Man® program. More detail about both models is provided in the Appendix. The second goal of this manuscript is to address the controversial issue whether or to what an extent distribution volumes and clearances relate to tissue volumes and blood flows. We therefore examined whether distribution volumes and clearances match the tissue volumes and blood flows from the physiological model used to generate the data from which the parameters of the compartmental model were derived.
Part I: Deriving the kinetic parameters of the compartmental model
Gas Man® was used to generate FA for 4 different agents (halothane, isoflurane, sevoflurane, and desflurane) during a wash-in and washout period of 115 min each with a high fresh gas flow (8 L.min-1) and a constant alveolar minute ventilation (4 L.min-1, regardless of patient weight). The default settings were used for the circuit and tissue composition. The inspired concentrations of halothane, isoflurane, sevoflurane, and desflurane were maintained constant during the wash-in period at 0.75; 1.15; 2; and 6% respectively. With each of these inspired concentrations, simulations were run for a 70 kg patient with 5 different cardiac outputs (2, 3, 5, 8 and 10 L.min-1) and for 5 patients with different weights (40, 55, 70, 85, and 100 kg) but the same cardiac output (5 L.min-1). This yielded 9 unique simulations for each agent (note that each group includes a 70 kg patient with a cardiac output of 5 L.min-1, which is why there were not 10 unique simulations). Two and three compartmental models were fitted to FA of the individual 9 simulations using NONMEM (the original data and the NONMEM control code are available in the Web supplement). The total administered dose was entered in the NONMEM data file as the product of the inspired concentration and duration. A naïve pooled data fit was done to obtain starting values for the structural parameters (distribution volumes and clearances) for each of the four agents. The effect of weight and cardiac output on each of the structural parameters (covariate analysis) was assessed using the minimum objective function of NONMEM, -2 × Log Likelihood (-2LL), to decide whether to accept or omit a covariate. The results were then tested for parsimony by sequentially deleting each of the covariate parameters using the NONMEM objective function as the criteria to accept or delete any covariate parameter. Goodness of fit was evaluated using median prediction error (MDPE) and median absolute prediction error (MDAPE) as a measure for bias and accuracy respectively . MDPE and MDAPE were calculated as (FAGas Man - FA3compartmental model)/FA3compartmental model) and |(FAGas Man - FA3compartmental model)/FA3compartmental model| respectively, and are expressed in %.
Part II: Prospective testing of the compartmental model
Using the previously derived parameters with their covariates, the compartmental model was tested prospectively by having it generate FA for a patient with parameters different from those from which the model was derived. The FA output for a 62 kg patient with a cardiac output of 4.5 L.min-1 for three different durations (wash-in and wash-out period of 10, 60, and 180 min each) with an FI of 1.5% halothane, 1.5% isoflurane, sevoflurane 4%, or desflurane 12% was calculated by converting the volume and clearance parameters, including any covariate effects, into the coefficients and exponents defining the three exponential functions that together describe the FA course. Conversions were done with the Excel spreadsheet CONVERT.XLS . The same patient parameter set was entered into Gas Man® and the respective end-expired concentrations were obtained. The predictive performance of the compartmental model was tested using MDPE and MDAPE as described above. MDPE and MDAPE less than 20% have been considered acceptable. All data and control files are available upon simple request to the authors (JHX).
The pharmacokinetic parameters for the three compartmental model with cardiac output (CO, L.min-1) and weight (WT, kg) as covariates (tested for parsimony).
V1 = 5.65 + 0.020(WT-70) + 0.68(CO-5)
V2 = 8.35 + 0.15(WT-70) - 0.49(CO-5)
V3 = 134.09 + 1.91(WT-70)
CL1 = 1.23 + 0.050(CO-5)
CL2 = 2.57 + 0.010(WT-70) + 0.47(CO-5)
CL3 = 0.87 + 0.17(CO-5)
V1 = 4.21 + 0.020(WT-70) + 0.39(CO-5)
V2 = 3.16 + 0.065(WT-70) - 0.31(CO-5)
V3 = 61.40 + 0.87(WT-70)
CL1 = 1.12 + 0.024(CO-5)
CL2 = 1.05 + 0.0037(WT-70) + 0.17(CO-5)
CL3 = 0.46 + 0.092(CO-5)
V1 = 3.33 + 0.018(WT-70) + 0.21(CO-5)
V2 = 1.51 + 0.033(WT-70) - 0.18(CO-5)
V3 = 33.69 + 0.47(WT-70)
CL1 = 1.05 + 0.011(CO-5)
CL2 = 0.37 + 0.0034(WT-70) + 0.053(CO-5)
CL3 = 0.23 + 0.046(CO-5)
V1 = 2.94 + 0.017(WT-70) + 0.14(CO-5)
V2 = 1.56 + 0.030(WT-70) - 0.14(CO-5)
V3 = 14.08 + 0.19(WT-70)
CL1 = 1.03 + 0.0066(CO-5)
CL2 = 0.25 + 0.0022(WT-70) + 0.036(CO-5)
CL3 = 0.14 + 0.029(CO-5)
Goodness of fit for the predictions by three compartment model predictions during model derivation and prospective testing.
The time course of FA of a potent inhaled anesthetic generated by a physiological uptake model (Gas Man®) can be equally well described using a classical three compartmental model derived from data generated by the very same physiological model (Gas Man®). While the relationship between the distribution volumes and clearances and organ capacities and tissue blood flows is complex, it is nevertheless intuitively tempting to try to explain e.g. the associations between a decrease in cardiac output and the changes in the volumes of distribution in terms of alterations in tissue blood flow of distributions. Yasuda and colleagues used NONMEM derived classical compartmental parameters from end-expired concentrations and related the parameters of the exponential curves (exponents and time constants) to known physiological processes and anatomical compartments . These parameters were subsequently used to help delineate several physiological compartments: the first, second, third, fourth, and fifth compartment were interpreted as representing lungs, vessel rich group, muscle group, intertissue diffusion, and the fat group. Hull, however, acclaims that while it is often suggested that some particular tissue or organ (such as the brain) be 'in' one compartment or another, such suggestions are ill-founded because parameters of the fit to the uptake data contain no information that might support such assumptions [10, 11]. Similarly, Wissing argues that a precise allocation of several hypothetical peripheral compartments to anatomical defined tissues is hardly feasible [2, 3].
If it is true that distribution volumes and clearances can be directly interpreted in terms of tissue volumes and tissue blood flows, a change in weight or cardiac output that is known to cause proportional changes in tissue volumes or tissue blood flow in the (physiological) model of Gas Man® should also cause proportional changes in the distribution volumes and clearances of the empirical compartmental (NONMEM) model. In our current simulations, an increase in cardiac output and weight does indeed increase clearance and distribution volume (Figures 1 and 2). However, this type of relationship is not consistent. An increase in cardiac output is associated with a decrease in the clearance of V2 (the second compartment) with sevoflurane and isoflurane. In addition, the non-linear (almost hyperbolic) relationship between V3 (the third compartment) and cardiac output for all four gases cannot be interpreted in terms of an underlying physiological model or process. Therefore, the parameters of the underlying physiological model (organ capacities and blood flows) and those of an empirical model (distribution volumes and clearances) therefore cannot be interpreted in terms of one another.
We have shown that the kinetics of anesthetic gases can be described by a mammilary model. Therefore, concepts that are traditionally thought of as being applicable to the kinetics of intravenous agents can be equally well applied to anesthetic gases. One example of one of these concepts are context sensitive half-times, which interestingly had been described for inhaled agents before the term context sensitive half-time was introduced but were labeled "coasting times" by Lowe and Ernst [12, 13].
This study does not address when or whether to use physiological modeling or classical compartmental modeling. Either modeling approach adequately describes and predicts the course of FA, but their parameters cannot be interpreted in terms of one another. A three compartment model can be a good fit of a concentration that is effectively the sum of a multi-organ (physiological) system, where each organ displays first order kinetics . This study does not address the validity of the GasMan® model either. Even though GasMan® can be used to gain additional insights into the kinetic of inhaled agents, clinical validation of the GasMan® model is lacking.
We describe how non-linear mixed-effect modeling can be used to derive a three compartmental empirical model to describe the kinetic behavior of potent inhaled anesthetic generated by a physiological model (Gas Man®). Therefore, concepts that are traditionally thought of as being applicable to the kinetics of intravenous agents can be equally well applied to anesthetic gases. The relationship between the distribution volumes and clearances of the empirical model and tissue capacities and blood flow of the physiological model are complex, however. Our study reinforces the fact that the compartmental models (even with co-variate models) are an empirical description of a data set, and that the parameters have virtually no physiological interpretation.
Appendix. Graphical display and formulas of the empirical three-compartmental model (NONMEM) and the physiological model of Gas Man®
The empirical three-compartmental model (NONMEM)
By using a sum of least squares method (the minimum objective function or MOF), NONMEM determines whether a one, two or three compartmental model best describes the concentration course. Depending on the type of control file used, NONMEM analysis will yield either the exponents and coefficients or distribution volumes and clearances. The best fitting model is then optimized by mathematically linking patient covariates (e.g. weight, height, cardiac output) to those parameters, again using the MOF to decide whether or not a covariate significantly improves the fit.
The physiological model of Gas Man®
The authors would like to thank Eger EI II, UCSF, CA, for reviewing the manuscript, even though not all of his suggestions have been incorporated.
- Lowe HJ, Ernst EA: The Quantitative Practice of Anesthesia – Use of a Closed Circuit. 1981, Baltimore/London: Williams & WilinsGoogle Scholar
- Hendrickx JFA, Soetens M, Van der Donck A, Meeuwis H, Smolders F, De Wolf AM: Uptake of desflurane and isoflurane during closed-circuit anesthesia with spontaneous and controlled ventilation. Anesth Analg. 1997, 84: 413-418. 10.1097/00000539-199702000-00032.PubMedGoogle Scholar
- Wissing H, Kuhn I, Rietbrock S, Fuhr U: Pharmacokinetics of inhaled anesthetics in a clinical setting: comparison of desflurane, isoflurane and sevoflurane. Br J Anaesth. 2000, 84: 443-449.View ArticlePubMedGoogle Scholar
- Rietbrock S, Wissing H, Kuhn I, Fuhr U: Pharmacokinetics of inhaled anesthetics in a clinical setting: description of a novel method based on routine monitoring data. Br J Anaesth. 2000, 84: 437-442.View ArticlePubMedGoogle Scholar
- Bouillon T, Shafer SL: Hot air or full steam ahead? An empirical pharmacokinetic model of potent inhalational agents [editorial]. Br J Anaesth. 2000, 84: 429-431.View ArticlePubMedGoogle Scholar
- Beal SL, Sheiner L: NONMEM Users Guide. 1980, San Francisco: University of CaliforniaGoogle Scholar
- Varvel JR, Donoho DL, Shafer SL: Measuring the predictive performance of computer-controlled infusion pumps. J Pharmacokinet Biopharm. 1992, 20: 63-94. 10.1007/BF01143186.View ArticlePubMedGoogle Scholar
- Yasuda N, Lockhart SH, Eger EI, Weiskopf RB, Johnson BH, Freire BA, Fassoulaki A: Kinetics of desflurane, isoflurane, and halothane in humans. Anesthesiology. 1991, 74: 489-498.View ArticlePubMedGoogle Scholar
- Hull CJ: Pharmacokinetics for Anaesthesia. 1997, Oxford: Butterworth Heinemann, 176-183, 209Google Scholar
- Shafer SL: Chapter 52. Principles of pharmacokinetics and pharmacodynamics. Principles and Practice of Anesthesiology. Edited by: Longnecker DE, Tinker JH, Morgan GE. 1998, St Louis: Mosby, 1173-2Google Scholar
- Lowe HJ, Ernst EA: The quantitative practice of anesthesia – use of closed circuit. 1981, Baltimore: Williams & WilkinsGoogle Scholar
- Eger EI, Shafer SL: Tutorial: context-sensitive decrement times for inhaled anesthetics. Anesth Analg. 2005, 101: 688-696. 10.1213/01.ANE.0000158611.15820.3D.View ArticlePubMedGoogle Scholar
- Van Liew HD: Semilogarithmic plots of data which reflect a continuum of exponential processes. Science. 1962, 138: 682-683.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2253/6/7/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.