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. 2006 Jul 21;63(1):75–84. doi: 10.1111/j.1365-2125.2006.02725.x

Table 1b.

Vancomycin population pharmacokinetic parameter estimates using a variable slope sigmoidal model relating postmenstrual age (PMA) to clearance (CL)

Parameter Estimate BSV BOV %SE
CLstd ‘mature’ (lh−170kg−1) and RF=1 3.79 0.209 0.122 20.2
Vstd (l70kg−1) 39.4 0.197 2.6
EMATCL50 (weeks) 33.3 28.3
HillCL 3.68 37.2
Fventilation (on CL) 1.03 3.6
Finotrope (on V) 1.18 10.8
Kage 0.00789 64.9
Residual unidentified variability additive 1.5mgl−1 32.1
proportional 0.23% 11.7

BSV and BOV are the between-subject and between-occasion variability expressed as the square root of their variance, SE is the standard error of the structural estimate. V = Vstd×(Wt/70) × Finotrope × Inot l. CL=CLstd × (Wt/70)0.75 × [PMAHillCL/(PMAHillCL + EMATCL50HillCL)]×RF×Fventilation×Vent lh−1where Vstd and CLstd are the population estimates for V and CL, respectively, standardized to a 70-kg person using allometric models; PMA is the postmenstrual age in weeks; EMATCL50 is the PMA at which clearance is 50% that of the mature value; HillCL is the Hill coefficient for clearance; Finotrope and Fventilation are scaling factors applied for the use of inotropes (Inot) or positive pressure artificial ventilation (Vent); Inot and Vent have a value of 1 if present and 0 if absent. The calculation of renal function (RF) is explained in the text.