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. Author manuscript; available in PMC: 2011 Aug 1.
Published in final edited form as: J Clin Psychopharmacol. 2010 Aug;30(4):404–410. doi: 10.1097/JCP.0b013e3181e66a62

Table 2.

Population pharmacokinetic estimates of lithium

Parameter (unit) Population estimate (between subject variability %)
Base modela Allometric scaling by total body weightb Allometric scaling by fat-free massc
CL (L/h) 1.34 (51.6) 1.50 (44.5) 1.79 (42.2)
V (L)d 39.7 (8.84) 63.4 (9.16) 56.4 (5.51)
T1/2abs (min) 29.3 (39.1) 27.6 (39.5) 29.9 (32.2)
Tlag (min) 16.8 (78.7) 17.5 (76.7) 17.4 (82.6)
T1/2α (h)e 2.66 (31.7) 2.96 (10.9) 2.43 (31.1)
T1/2β (h)f 27.3 (41.0) 36.2 (25.3) 27.4 (28.4)
CVcp (%) 38.1 39.4 38.6
SDcp (mEq/L) 0.1 (fixed) 0.1 (fixed) 0.1 (fixed)
a

no covariate included

b

CL, V, and T1/2β allometrically scaled based on a standard total body weight of 70 kg to allow comparison to results from adult trials

c

CL, V, and T1/2β allometrically scaled based on a standard fat-free mass of 53 kg

d

V: total volume of distribution (Vc + Vp), average (%CV) calculated from individual parameter estimates of Vc and Vp

e

average (% coefficient of variation) half-life of the α-phase calculated from individual population parameter estimates

f

average (% coefficient of variation) terminal half-life calculated from individual population parameter estimates