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. 2016 Mar 25;60(4):2150–2156. doi: 10.1128/AAC.02592-15

TABLE 5.

Bootstrap validation of the population pharmacokinetic parameters

Model parameterb Final estimate ± SE Bootstrap validation (n = 1,000)a
θ1 (liters/h/kg0.75) 0.395 ± 0.049 0.396 (0.315 to 0.550)
θ2 (liters/kg) 0.406 ± 0.023 0.404 (0.361 to 0.451)
θ3 0.460 ± 0.020 0.452 (0.002 to 0.487)
θ4 (liters/h/kg0.75) 0.575 ± 0.049 0.580 (0.488 to 2.570)
θ5 0.705 ± 0.039 0.705 (0.598 to 0.785)
θ6 1.09 ± 0.087 1.09 (0.945 to 1.320)
θ7 0.010 ± 0.003 0.010 (0.004 to 0.016)
θ8 −0.392 ± 0.101 −0.396 (−0.620 to −0.191)
θ9 −0.548 ± 0.221 −0.555 (−1.01 to −0.106)
%ωCL 31.80 ± 12.90 30.6 (25.1 to 35.8)
%ωVss 22.20 ± 12.60 21.1 (14.1 to 28.7)
66.30 ± 37.30 66.1 (48.6 to 98.8)
a

Values are medians (2.5th to 97.5th percentile). The success rate was 86.9%.

b

θ1, TVCL after maturation; θ2, TVVss; θ3, ratio of TVV/TVVss; θ4, typical value of intercompartmental clearance; θ5, fraction of additive and proportional error; θ6, fraction of mature CL at birth; θ7, rate constant for CL gain; θ8, exponent for serum creatinine for CL; θ9, exponent for gestational age for Vss. CL, clearance; Vss, steady-state volume of distribution.