Skip to main content
. 2016 Dec 22;56(9):1045–1055. doi: 10.1007/s40262-016-0492-2

Table 3.

Parameter estimates of the population pharmacokinetic model

Parameter Units Estimate RSEa, % Description
CLKOV dL/h 1.51 7.33 Clearance of BAY 81-8973
V1KOV,ADV dL 23.6 2.76 Central volume of distribution of BAY 81-8973 and rAHF-PFM
QKOV,ADV dL/h 1.59 5.5 Intercompartmental clearance of BAY 81-8973 and rAHF-PFM
V2KOV dL 5.35 12.8 Peripheral volume of distribution of BAY 81-8973
ΔCLADV % 47.8 8.05 Change in clearance for rAHF-PFM compared with BAY 81-8973
ΔV2ADV % 86.6 23.4 Change in peripheral volume of distribution for rAHF-PFM compared with BAY 81-8973
IIVCl CV %b 27.2 13.9 Intraindividual variability in clearance
IIVV1 CV %b 7.93 36.9 Intraindividual variability in central volume of distribution
IIVΔCl CV %b 35 27.1 Intraindividual variability in change in clearance
IOVF1 CV %b 10.3 31.7 Intraoccasional variability in bioavailability
εprop CV %c 5.73 6.84 Proportional residual error

CV coefficient of variation, rAHF-PFM antihemophilic factor (recombinant) plasma/albumin-free method, RSE relative standard error, SQRT square root

aAssessed via bootstrap (n = 500, with 485 successful runs)

bCalculated by SQRT(EXP(variance) − 1) × 100

cCalculated by SQRT(variance) × 100