The urea kinetic model is used to monitor the dialysis and dietary protein prescriptions. Because patient urea distribution volume (V) is difficult to measure, it is usualyasumed to be 58 % of body weight although total body water may vary between 35 and 75 % of body weight. In this study we have calculated V by a precise method, by direct quantitation of urea in dialysate and have-determined whater dialysis characteristics modify V. Twenty patients, ten male and 10 female, on thrice weekly dialysis (3 hours/session) were studied. All dialysate was collected in a graduated 120 litertank. Urea concentration in blood and dialysate was measured hourly and V calculated. In each patient we performed 6 dialysis in which blood flow (250 or 350 ml/hr), ultrafiltration (0.5 or 1.5 l/h), membrane or buffer (bicarbonate or acetate) was varied. At the end of haemodialysis V varied between 43 and 72 % of body weigh, but in each patient this value was practically constant. V increased during haemodialysis, 41.7 +/- 7.1 % in the first hour, 50.4 +/- 7.5 in second hour and 55.5 +/- 7.9 % in the third hour. This data suggest a bi or multicompartmental urea kinetic model. The blood flow, ultrafiltration, membrane or buffer did not influence the results. V was significantly increased in males as compared to females, 60.5 +/- 6.1 % versus 50.9 +/- 6.1 % (p < 0.01).