B. Rippe, PATHOPHYSIOLOGICAL DESCRIPTION OF THE ULTRASTRUCTURAL-CHANGES OF THE PERITONEAL MEMBRANE DURING LONG-TERM CONTINUOUS AMBULATORY PERITONEAL-DIALYSIS, Blood purification, 12(4-5), 1994, pp. 211-220
Some of the patients on continuous ambulatory peritoneal dialysis (CAP
D) develop with time on treatment an increased transperitoneal transpo
rt of small solutes, implying that glucose is more rapidly absorbed fr
om the dialysate. Hence, the dialysate/serum crystalloid osmotic gradi
ent dissipates at a faster rate, so that ultrafiltration failure may r
esult. The pathophysiological correlates to these changes are not well
understood. However, it seems that with time on CAPD, there are chang
es in the submesothelial interstitium, affecting both the ground subst
ance and spacing and orientation of collagen fibers. There may also be
mesothelial alterations with patchy shedding of the cells. The presen
t article discusses these changes in terms of a modified three-pore mo
del of peritoneal permeability. In this model, the capillary walls act
as a major barrier for solutes ranging in size from inulin (molecular
radius 14 Angstrom) to macromolecules (molecular radius >30 Angstrom.
However, for solutes smaller than inulin both capillary wall and inst
erstitium contribute to the blood-peritoneum transport impedance. The
increased small-solute exchange sometimes occurring in long-term CAPD
can be explained either by recruitment of vascular surface area, due,
e.g., to an increased capillarization of the peritoneal membrane with
time, or, more likely, a drop in the interstitial transport resistance
to small solutes. The latter possibility is supported by the often mo
re pronounced increase in the transperitoneal transfer of small solute
s than that of macromolecules over time in CAPD.