We analytically solved the equation of the Variable volume, two-compar
tment solute kinetic model (TCSKM). From the solution, we constructed
an expression of weekly concentration profiles developing in the patie
nt's body by routine hemodialyses. Obtained formulas can be used to ca
lculate Kt/V, solute reduction index (SRI), the solute generation rate
(G) per unit distribution volume (V), and a mass transfer coefficient
(MTC) between the two compartments. To estimate these parameters, the
formulas only need three-point data during a dialysis, that is, pre-,
one-hour, and post-dialysis solute concentrations instead of four tha
t would otherwise be needed. A 48 hour data point is not required. The
weekly concentration profiles can be easily calculated by the formula
s. As examples of clinical applications, we calculated Kt/V, G/V, and
SRI of urea, Cr, and uric acid using plasma data of 121 hemodialyzed p
atients. Then the results were compared with the single-compartment so
lute kinetic model (SCSKM). The obtained mean MTC/V values, that is, 1
.08 (1/hr) for urea, 0.53 (1/hr) for Cr, and 1.11 (1/hr) for uric acid
, were consistent with the previous works. SCSKM overestimated the mea
n G/V by 7.1%, 15.9%, and 10.0%, and the mean SRI by 6.7%, 18.6%, and
10.0%, for urea, Cr, and uric acid, respectively. The solute distribut
ion volume ratio of TCSKM to SCSKM, (V)(TCSKM)/(V)(SCSKM), depended on
the value of MTC/V and the hemodialysis duration. Using pedometers, w
e measured the total number of steps the patients took during a week.
We found that the total number of steps in a week was significantly co
rrelated with the Cr generation rate (r = 0.285, P < 0.03), but that i
t was not significantly correlated with the other generation rates (r
= 0.204, P > 0.09 for urea, and r = 0.209, P > 0.08 for uric acid). Th
ese data suggest that the Cr generation rate is related to the patient
's physical activity. We conclude that the formulas can estimate an ad
equate dialysis prescription for the hemodialyzed patient.