Analytical Solution of Multicompartment Solute Kinetics for Hemodialysis

Author:

Korohoda Przemysław1ORCID,Schneditz Daniel2

Affiliation:

1. AGH University of Science and Technology, Faculty of Computer Science, Electronics and Telecommunications, Department of Electronics, al. A. Mickiewicza 30, 30-059 Krakow, Poland

2. Institute of Physiology, Center for Physiological Medicine, Medical University of Graz, Harrachgasse 21/5, 8010 Graz, Austria

Abstract

Objective.To provide an exact solution for variable-volume multicompartment kinetic models with linear volume change, and to apply this solution to a 4-compartment diffusion-adjusted regional blood flow model for both urea and creatinine kinetics in hemodialysis.Methods.A matrix-based approach applicable to linear models encompassing any number of compartments is presented. The procedure requires the inversion of a square matrix and the computation of its eigenvaluesλ, assuming they are all distinct. This novel approach bypasses the evaluation of the definite integral to solve the inhomogeneous ordinary differential equation.Results.For urea two out of four eigenvalues describing the changes of concentrations in time are about 105times larger than the other eigenvalues indicating that the 4-compartment model essentially reduces to the 2-compartment regional blood flow model. In case of creatinine, however, the distribution of eigenvalues is more balanced (a factor of 102between the largest and the smallest eigenvalue) indicating that all four compartments contribute to creatinine kinetics in hemodialysis.Interpretation.Apart from providing an exact analytic solution for practical applications such as the identification of relevant model and treatment parameters, the matrix-based approach reveals characteristic details on model symmetry and complexity for different solutes.

Publisher

Hindawi Limited

Subject

Applied Mathematics,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,Modelling and Simulation,General Medicine

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