Pharmacokinetic Training Packet for Pharmacists Revised 1/09, 6/12 Original document compiled by: Elizabeth D. Hermsen, Pharm.D., M.B.A., BCPS-ID Updated by: Alan Gross, Pharm.D., BCPS Thanks to Erin Iselin, Scott McMullen, Chris Shaffer, & Keith Olsen for your thoughtful review! Any questions? Call or email Alan Gross at 559-4149/
[email protected] Table of Contents Pharmacokinetic definitions and principles 3 Aminoglycoside overview 4 Extended-interval (Once daily) aminoglycoside dosing 8 Aminoglycoside pharmacokinetic calculations 10 Aminoglycoside dosing in patients with cystic fibrosis 12 Vancomycin overview and pharmacokinetic calculations 15 Clinical Pearls 21 Dialysis – Aminoglycosides and Vancomycin 21 TNMC Nephrology Protocol for Vancomycin Dosing 21 Clinical Pharmacokinetic Consult Service 23 2 Pharmacokinetic Definitions and Principles Kel, Ke, or Kd or Elimination Rate Constant 1 • The fraction or percentage of the total amount of drug in the body eliminated per unit of time. • Estimated with 2 drug levels taken between doses (the slope of the line). To be accurate, 2-4 half-lives should occur between the levels.1 -kel(τ) • In pharmacokinetic calculations, the term e represents the fraction of the serum concentration that remains. Thus, 1 - e- kel(τ) represents the fraction of the serum concentration that is eliminated. t 1/2 or Half-life 1 • The time required for the TOTAL amount of remaining drug in the body to decline by 50%. • Sometimes referred to as β t ½ to distinguish it from the distribution half-life, α t ½, used in two compartment modeling.1 Peak, C max1 • C max is the maximum measurable drug concentration at the end of an infusion BEFORE significant distribution occurs.