Urea kinetic modelling: comparison of three methods. 1989

R Vanholder, and P Van Trimpont, and S Ringoir
Nephrology Department, University Hospital, Ghent, Belgium.

It has been claimed that computed urea kinetic (UK) modelling in haemodialysed patients for the estimation of protein intake and of the relation between total dialyser urea clearance and distribution volume (Kt/V) leads to an overestimation of protein catabolic rate (PCR). In the present study three different methods of kinetic modelling for the determination of PCR and Kt/V are compared in 15 patients. The first method (MI) is the direct quantification method based on the collection of all urea eliminated from the body. The two other methods are based on an iterative computed calculation. The second method (MII) is the urea kinetic modelling method as described by Sargent. Dialyser clearances were measured directly and not estimated by theoretical extrapolation. The third method described here (MIII), is based on the indirect calculation of urea distribution volume (Vw) according to Watson and of dialyser clearances from this Vw and from pre- and post-dialysis urea concentrations. All three methods result in PCRs that are not significantly different (MI: 1.04 +/- 0.29; MII: 1.07 +/- 0.28; MIII: 1.05 +/- 0.24 mg/kg BW per 24 h; p greater than 0.05). When the results are correlated, the following results are obtained: MI vs MII: r = 0.76, p less than 0.001; MI vs MIII: r = 0.78, p less than 0.001; MII vs MIII: r = 0.90, p less than 0.001. For Kt/V virtually identical results were obtained for each of the methods under study. In conclusion, all methods under study seem equally reliable in determining mean PCR.(ABSTRACT TRUNCATED AT 250 WORDS)

UI MeSH Term Description Entries
D007700 Kinetics The rate dynamics in chemical or physical systems.
D008297 Male Males
D008657 Metabolic Clearance Rate Volume of biological fluid completely cleared of drug metabolites as measured in unit time. Elimination occurs as a result of metabolic processes in the kidney, liver, saliva, sweat, intestine, heart, brain, or other site. Total Body Clearance Rate,Clearance Rate, Metabolic,Clearance Rates, Metabolic,Metabolic Clearance Rates,Rate, Metabolic Clearance,Rates, Metabolic Clearance
D008954 Models, Biological Theoretical representations that simulate the behavior or activity of biological processes or diseases. For disease models in living animals, DISEASE MODELS, ANIMAL is available. Biological models include the use of mathematical equations, computers, and other electronic equipment. Biological Model,Biological Models,Model, Biological,Models, Biologic,Biologic Model,Biologic Models,Model, Biologic
D011506 Proteins Linear POLYPEPTIDES that are synthesized on RIBOSOMES and may be further modified, crosslinked, cleaved, or assembled into complex proteins with several subunits. The specific sequence of AMINO ACIDS determines the shape the polypeptide will take, during PROTEIN FOLDING, and the function of the protein. Gene Products, Protein,Gene Proteins,Protein,Protein Gene Products,Proteins, Gene
D005260 Female Females
D006435 Renal Dialysis Therapy for the insufficient cleansing of the BLOOD by the kidneys based on dialysis and including hemodialysis, PERITONEAL DIALYSIS, and HEMODIAFILTRATION. Dialysis, Extracorporeal,Dialysis, Renal,Extracorporeal Dialysis,Hemodialysis,Dialyses, Extracorporeal,Dialyses, Renal,Extracorporeal Dialyses,Hemodialyses,Renal Dialyses
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D014508 Urea A compound formed in the liver from ammonia produced by the deamination of amino acids. It is the principal end product of protein catabolism and constitutes about one half of the total urinary solids. Basodexan,Carbamide,Carmol

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