Kinetic modeling of peritoneal transport.
Explore the source record for details and available documents.
Biomedical subjects
Publications and source records attributed to J W Moncrief.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
The technique of continuous ambulatory peritoneal dialysis was evaluated in nine patients during 136 patient weeks. The major objectives were to see if continuous ambulatory peritoneal dialysis would provide [1] acceptable control of serum chemistries by usual criteria, [2] adequate removal of sodium and water, [3] tolerable protein losses, and [4] a low prevalence of peritonitis with episodes responsive to therapy with continuing continuous ambulatory peritoneal dialysis. Preliminary findings suggest continuous ambulatory peritoneal dialysis represents an effective ambulatory, portable, internal dialysis technique. Larger-solute clearances per week may approach values six times greater than with most hemodialysis techniques. Small-solute clearances approach dialysate flow rate (8.3 ml/min) and are comparable to other dialysis techniques on a weekly basis. Edema is readily controlled and protein losses should be tolerable with adequate protein intake. Peritonitus occurs on the average every 10 weeks but responds to therapy promptly with continuing continuous ambulatory peritoneal dialysis. If the prevalence of peritonitis can be reduced, continuous ambulatory peritoneal dialysis appears to represent a very attractive dialysis technique.
Explore the source record for details and available documents.
The transmittance coefficients of Cuprophan PT-150 and Rhone-Poulenc AN69 have been defined over a broad MW range. The results can be completely characterized by a simple Gaussian distribution employing 2 parameters, the selectivity and the mean molecular diameter. The selectivities of the membranes studies are identical. The mean MW at 50% cutoff for Cuprophan and RP69 are 2,500 and 11,500, respectively. A membrane model illustrating a semi-empirical correlation between permeability and transmittance has been developed.
Explore the source record for details and available documents.
A diffusion limited, multicompartment patient-artifical kidney transport model has been developed. The physiological transport parameters have been clincially elevated for radiosotopically tagged urea, creatinine, uric acid, vitamin B12, and inulin with anuric, chronic uremic patients. Concomitant hemodialysis simulations illustrate that a 3 compartment patient model is adequate to characterize physiological transport. However, because of the high value of the transcapillary mass transfer coefficient, it is concluded that a 2 compartment (intracellular/extracellular) model is adequate to define mass transfer in the patient-artifical kidney system: a single pool may be assumed for very low hemodialyzer (less than 20 ml/min) clearances. Dialysis simulations also demonstrate that a point of diminshing returns is reached with respect to increasing mass removal from the patient, via increasing dialyzer clearance for middle molecules. In a 5 hr hemodialysis simulation the system becomes limited by physiological mass transfer resistances for dialyzer clearances greater than 100 ml/min. It is concluded that physiological transport resistances significantly impeded the removal of middle molecules from the patient-artifical kidney system. As a result, a single, well mixed pool assumption is not generally adequate to describe solute transport. A consequence of this conclusion is that the M2-hr hypothesis, which is based on a single pool assumption, cannot be generally utilized to accurately adjust hemodialysis treatment schedules for equivalent middle molecule removal. We are currently analyzing the patient-artifical kidney system to define improved adjustments modes for equivalent mass removal employing a 2 pool patiemt model.
Explore the source record for details and available documents.