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. 2005 Sep;60(3):276–286. doi: 10.1111/j.1365-2125.2005.02436.x

Table 2.

Parameter estimates for the final pharmacokinetic model for indinavir and the results of bootstrap analysis

Basic model Final model Bootstrap analysis
Est RSE (%) Est RSE (%) Median 95% PI
CL/F (l h−1) 49.3 6.19 46.8 5.75 46.6 41.5, 55.3
 θritonavir* 0.362 7.27 0.354 6.07 0.357 0.314, 0.406
 θconcomitant NNRTI* 1.41 4.78 1.41 1.27, 1.56
V/F (l) 77.2 5.03 82.3 4.70 81.8 74.4, 102.
ka (h−1) 2.64 16.4 2.62 16.0 2.59 1.90, 3.93
Lag-time (h)# 0.483 2.40 0.485 1.79 0.485 0.431, 0.545
IIV CL/F (%) 34.8 24.1 24.2 44.5 24.4 11.2, 52.3
IIV V/F (%) 28.5 50.6 24.6 52.3 24.0 10.6, 77.7
Correlation IIV CL/F-V/F 0.729 44.4 0.629 84.8 0.757 −1, 1-
IOV CL/F (%) 21.2 40.6 20.9 37.0 20.5 11.5, 32.6
IOV F (%) 22.8 48.3 23.1 50.7 22.2 7.74, 56.5
 θfemale* 1.48 16.7 1.46 0.882, 2.040
Additive error (mg l−1) 0.0491 17.0 0.0491 16.7 0.0492 0.0306, 0.0782
Proportional error (%) 35.0 6.06 35.3 6.18 34.8 25.0, 39.4
*

Relative change in pharmacokinetic parameter in the presence of the covariate, resulting in the following equations: CL/F = 46.8 × 0.354RTV × 1.41NNRTI, V/F = 77.2, F = 1 × 1.48SEX.

#

Only estimated when indinavir and ritonavir were combined. CL/F = clearance, V/F = volume of distribution, F = apparent bioavailability, ka = absorption rate constant, IIV = interindividual variability, IOV = interoccasion variability, Est = parameter estimate, RSE = relative standard error, PI = prediction interval.