PD does not require direct access to the circulation; rather, it obligates placement of a peritoneal catheter that allows infusion of a dialysate solution into the abdominal cavity; this allows transfer of solutes (i.e., urea, potassium, other uremic molecules) across the peritoneal membrane, which serves as the artificial kidney. This solution is similar to that used for hemodialysis, except that it must be sterile, and it uses lactate, rather than bicarbonate, to provide base equivalents. PD is far less efficient at cleansing the bloodstream than hemodialysis and therefore requires a much longer duration of therapy. Pts generally have the choice of performing their own exchanges (2-3 L of dialysate, four to five times during daytime hours) or using an automated device at night. Compared with hemodialysis, PD offers the major advantages of (1) independence and flexibility, and (2) a more gentle hemodynamic profile, with better preservation of residual renal function.
Complications are outlined in Table 140-2. Peritonitis is the most important complication. The clinical presentation typically consists of abdominal pain and cloudy dialysate; peritoneal fluid leukocyte count is typically >100/µL, 50% neutrophils. In addition to the negative effects of the systemic inflammatory response, protein loss is magnified severalfold during the peritonitis episode. If severe or prolonged, an episode of peritonitis may prompt removal of the peritoneal catheter or even discontinuation of the modality (i.e., switch to hemodialysis). Gram-positive organisms (especially Staphylococcus aureus and other Staphylococcus spp.) predominate; Pseudomonas or fungal (usually Candida) infections tend to be more resistant to medical therapy and typically obligate catheter removal. Antibiotic administration may be intravenous or intraperitoneal when intensive therapy is required.
For a more detailed discussion, see Liu KD, Chertow GM: Dialysis in the Treatment of Renal Failure: Chap. 336, p. 1822, in HPIM-19. |