Quantifying the effect of changes in the hemodialysis prescription on effective solute removal with a mathematical model.

One potential benefit of chronic hemodialysis (HD) regimens of longer duration or greater frequency than typical three-times-weekly schedules is enhanced solute removal over a relatively wide molecular weight spectrum of uremic toxins. This study assesses the effect of variations in HD frequency (F: per week), duration (T: min per treatment), and blood/dialysate flow rates (QB/QD: ml/min) on steady-state concentration profiles of five surrogates: urea (U), creatinine (Cr), vancomycin (V), inulin (I), and beta2-microglobulin (beta2M). The regimens assessed for an anephric 70-kg patient were: A (standard): F = 3, T = 240, QB = 350, QD = 600; B (daily/short-time): F = 7, T = 100, QB = 350, QD = 600; C/D/E (low-flow/long-time): F = 3/5/7, T = 480, QB = 300, QD = 100. HD was simulated with a variable-volume double-pool model, which was solved by numerical integration (Runge-Kutta method). Endogenous generation rates (G) for U, Cr, and beta2M were 6.25, 1.0, and 0.17 mg/min, respectively; constant infusion rates for V and I of 0.2 and 0.3 mg/min, respectively, were used to simulate middle molecule (MM) G values. Intercompartment clearances of 600, 275, 125, 90, and 40 ml/min were used for U, Cr, V, I, and beta2M, respectively, For each solute/regimen combination, the equivalent renal clearance (EKR: ml/min) was calculated as a dimensionless value normalized to the regimen A EKR, which was 13.4, 10.8, 6.6, 3.7, and 4.8 ml/min for U, Cr, V, I, and beta2M, respectively. For regimens B, C, D, and E, respectively, these normalized EKR values were U: 1.04, 0.96, 1.58, and 2.22; Cr: 1.03, 1.08, 1.80, and 2.55; V: 1.06, 1.32, 2.21, and 3.12; I: 1.05, 1.54, 2.57, and 3.62; beta2M: 1.00, 1.27, 1.73, and 2.19. The extent of post-HD rebound (%) was highest for regimens A and B, ranging from 16% (urea) to 50% (inulin), and lowest for regimen E, ranging from 6% (urea) to 28% (beta2M). The following conclusions can be made: (1) Relative to a standard three-times-weekly HD regimen of approximately the same total (weekly) treatment duration, a daily/short-time regimen results in modest (3 to 6%) increases in effective small solute and MM removal. (2) Relative to a standard three-times-weekly HD regimen, a three-times-weekly low-flow/long-time regimen results in comparable effective small solute removal and progressive increases in MM and beta2M removal. A daily low-flow/long-time regimen substantially increases the effective removal of all solutes.

[1]  P. A. Peterson,et al.  Turnover in humans of β2‐microglobulin: the constant chain of HLA‐antigens , 1971 .

[2]  E. Klein,et al.  Evaluation of two pool model for prediciting serum creatinine levels during intra- and inter-dialytic periods. , 1975, Transactions - American Society for Artificial Internal Organs.

[3]  Moncrief Jw,et al.  The consequences of physiological resistances on metabolite removal from the patient-artifical kidney system. , 1975 .

[4]  T. H. Frost,et al.  Kinetics of hemodialysis: a theoretical study of the removal of solutes in chronic renal failure compared to normal health. , 1977, Kidney international.

[5]  K. Schindhelm,et al.  Patient-hemodialyzer interactions. , 1978, Transactions - American Society for Artificial Internal Organs.

[6]  Heterogeneity of interstitial fluid space demonstrated by simultaneous kinetic analysis of the distribution and elimination of inulin and gallamine. , 1982, The Journal of pharmacology and experimental therapeutics.

[7]  L. Pedrini,et al.  Causes, kinetics and clinical implications of post-hemodialysis urea rebound. , 1988, Kidney international.

[8]  J. Rotschafer,et al.  Vancomycin pharmacokinetics in patients with various degrees of renal function , 1988, Antimicrobial Agents and Chemotherapy.

[9]  Kinetic analysis of beta-2-microglobulin behavior for hemodialysis patients. , 1988 .

[10]  Of time, TACurea, and treatment schedules. , 1988, Kidney international. Supplement.

[11]  N. Levin,et al.  Kinetics of beta-2-microglobulin in hemodialysis. , 1989, Contributions to nephrology.

[12]  Difference in beta 2-microglobulin removal between cellulosic and synthetic polymer membrane dialyzers. , 1990, ASAIO transactions.

[13]  Beta-2-microglobulin generation rate and clearance rate in maintenance hemodialysis patients. , 1990, Nephron.

[14]  J. Floege,et al.  Clearance and synthesis rates of beta 2-microglobulin in patients undergoing hemodialysis and in normal subjects. , 1991, The Journal of laboratory and clinical medicine.

[15]  M J Lysaght,et al.  Kinetic modeling as a prescription aid in peritoneal dialysis. , 1991, Blood purification.

[16]  K. Schindhelm,et al.  Beta2-microglobulin kinetics in end-stage renal failure , 1991 .

[17]  D. Sahm,et al.  Vancomycin elimination during high-flux hemodialysis: kinetic model and comparison of four membranes. , 1992, American journal of kidney diseases : the official journal of the National Kidney Foundation.

[18]  B. Charra,et al.  Survival as an index of adequacy of dialysis. , 1992, Kidney international.

[19]  Urea rebound and residual renal function in the calculation of Kt/V and protein catabolic rate. , 1993, Kidney international. Supplement.

[20]  W R Clark,et al.  Membrane adsorption of beta 2-microglobulin: equilibrium and kinetic characterization. , 1994, Kidney international.

[21]  B. Maroni,et al.  Vancomycin redistribution: dosing recommendations following high-flux hemodialysis. , 1994, Kidney international.

[22]  J. Bosch,et al.  Measurement of kinetic parameters for urea in end-stage renal disease patients using a two-compartment model. , 1994, Journal of the American Society of Nephrology : JASN.

[23]  P. Keshaviah,et al.  A New Approach to Dialysis Quantification: An Adequacy Index Based on Solute Removal , 1994 .

[24]  J T Daugirdas,et al.  A nomogram approach to hemodialysis urea modeling. , 1994, American journal of kidney diseases : the official journal of the National Kidney Foundation.

[25]  A. Zydney,et al.  Importance of convection in artificial kidney treatment. , 1994, Contributions to nephrology.

[26]  N W Levin,et al.  Is intercompartmental urea clearance during hemodialysis a perfusion term? A comparison of two pool urea kinetic models. , 1995, Journal of the American Society of Nephrology : JASN.

[27]  K. Sakai,et al.  An estimate of beta 2-microglobulin deposition rate in uremic patients on hemodialysis using a mathematical kinetic model. , 1995, Kidney international.

[28]  R. Toto,et al.  Accuracy of urea removal estimated by kinetic models. , 1995, Kidney international.

[29]  J T Daugirdas,et al.  Overestimation of hemodialysis dose depends on dialysis efficiency by regional blood flow but not by conventional two pool urea kinetic analysis. , 1995, ASAIO journal.

[30]  F. Casino,et al.  The equivalent renal urea clearance: a new parameter to assess dialysis dose. , 1996, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

[31]  Rodney S. Kenley Tearing down the barriers to daily home hemodialysis and achieving the highest value renal therapy through holistic product design. , 1996, Advances in renal replacement therapy.

[32]  K. Farrington,et al.  The post-hemodialysis rebound: predicting and quantifying its effect on Kt/V. , 1996, Kidney international.

[33]  R Charbonneau,et al.  Postdialysis urea rebound: determinants and influence on dialysis delivery in chronic hemodialysis patients. , 1996, American journal of kidney diseases : the official journal of the National Kidney Foundation.

[34]  S. Vas,et al.  Slow nocturnal home hemodialysis at the Wellesley Hospital. , 1996, Advances in renal replacement therapy.

[35]  C A Shanks,et al.  Recirculatory pharmacokinetic models of markers of blood, extracellular fluid and total body water administered concomitantly. , 1996, The Journal of pharmacology and experimental therapeutics.

[36]  F. Marumo,et al.  Quasi-steadiness approximation for the two-compartment solute kinetic model. , 1997, Kidney international.

[37]  J T Daugirdas,et al.  Comparison of methods to predict equilibrated Kt/V in the HEMO Pilot Study. , 1997, Kidney international.

[38]  Death on dialysis and the time/flux trade-off. , 1997, Blood purification.

[39]  J. Moran,et al.  Discrepancies between Urea Ktn versus Normalized Creatinine Clearance , 1997, Peritoneal dialysis international : journal of the International Society for Peritoneal Dialysis.

[40]  J. Scott Bioavailability of vitamin B12. , 1997, European journal of clinical nutrition.

[41]  J T Daugirdas,et al.  Hemodialyzer mass transfer-area coefficients for urea increase at high dialysate flow rates. The Hemodialysis (HEMO) Study. , 1997, Kidney international.

[42]  W. Clark,et al.  Vancomycin mass transfer characteristics of high-flux cellulosic dialysers. , 1997, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

[43]  M. Rocco,et al.  Quantification of hemodialysis: analysis of methods and the relevance to patient outcome. , 1997, Blood purification.

[44]  M. Büchler,et al.  Cytokines in Surgical Trauma: Cholecystectomy as an Example , 1998, Digestive Surgery.