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. Author manuscript; available in PMC: 2019 Oct 1.
Published in final edited form as: Paediatr Drugs. 2018 Oct;20(5):483–495. doi: 10.1007/s40272-018-0305-1

Table 3.

Individual empiric Bayesian post-hoc parameter estimates for pantoprazole in children, excluding the CYP2C19 poor metabolizer (PM).

Variable N CL/F
(L/kg TBW/h)
CL/F
(L/h)
CL/F
(L/h for 70kg TBW)
Vss/Fb
(L/kg TBW)
Half-life
(h)
Age
 6–11 years 18 0.11 (0.06–0.20) 6.13 (2.64–13.19) 7.50 (4.04–12.19) 0.11 0.90 (0.65–1.39)
 12–17 years 19 0.09 (0.04–0.15) 9.07 (3.65–16.71) 7.01 (3.16–11.30) 0.11 1.09 (0.81–1.94)
2C19 genotype
 Poor metabolizers 1 0.02 1.29 1.47 0.11 3.60
 Intermediate metabolizer 16 0.09 (0.04–0.13) 6.00 (2.64–11.62) 6.73 (3.16–7.97) 0.11 1.10 (0.82–1.94)
 Extensive metabolizer 21 0.11 (0.06–0.20) 8.97 (4.66–16.71) 7.98 (5.03–12.19) 0.11 0.95 (0.65–1.45)

Data are presented as median (range). Vss/F was calculated as a sum of Vc/F and Vp/F. All participants had the same TBW normalized Vss/F as no inter-individual variability was estimated on Vc and Vp in the final model.

CL/F, apparent clearance; TBW, total body weight; Vss/F, steady-state volume of distribution.