Joachim Böhler, M.D., Johannes Donauer, Frieder Keller 

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Pharmacokinetic principles during continuous renal replacement therapy: Drugs and dosage  Joachim Böhler, M.D., Johannes Donauer, Frieder Keller  Kidney International  Volume 56, Pages S24-S28 (November 1999) DOI: 10.1046/j.1523-1755.56.s.72.2.x Copyright © 1999 International Society of Nephrology Terms and Conditions

Figure 1 Continuous renal replacement therapy (CRRT) results in different drug clearance rates depending on the treatment modality used. (A) In postdilution hemofiltration, ultrafiltrate is saturated to 100% compared with the drug concentration in plasma water. The drug clearance equals the ultrafiltration rate. (B) In predilution hemofiltration, the drug concentration is diluted by substitution fluid prior to entry into the dialyzer, resulting in a lower saturation of ultrafiltrate compared with the patient's plasma water. The clearance is lower than the ultrafiltrate flow rate. (C) In continuous hemodialysis, diffusion of the free non-protein-bound fraction of the drug is variable and depends mainly on the molecular weight of the drug. Kidney International 1999 56, S24-S28DOI: (10.1046/j.1523-1755.56.s.72.2.x) Copyright © 1999 International Society of Nephrology Terms and Conditions

Figure 2 Drug clearance by diffusion in continuous hemodialysis. Diffusion of the free non-protein-bound fraction of the drug into the dialysate depends on molecular weight. Although drug clearance increases with higher dialysate flow rates, clearance of larger molecules benefits less from higher dialysate flow rates. Kidney International 1999 56, S24-S28DOI: (10.1046/j.1523-1755.56.s.72.2.x) Copyright © 1999 International Society of Nephrology Terms and Conditions