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Clinical |
Division of Nephrology,1 Department of Medicine, Academic Medical Center, University of Amsterdam, Amsterdam; Dianet Foundation Amsterdam-Utrecht,2 The Netherlands
Correspondence to: A. Parikova, Clinic of Nephrology, 1st Faculty of Medicine, Charles University, U nemocnice 2, 120 00 Prague 2, Czech Republic. Alenaparikova{at}hotmail.com
Background: Peritoneal function tests are performed in
peritoneal dialysis (PD) patients to characterize peritoneal membrane status.
A low pH/high glucose degradation product (GDP) dialysis solution is used as
the test solution. The objective of the present study was to compare a 3.86%
glucose, low pH/high GDP dialysis solution (pH 5.5) with a 3.86% glucose,
normal pH/low GDP dialysis solution (pH 7.4) in assessments of peritoneal
membrane function.
Methods: Two standard peritoneal permeability analyses
(SPA) were performed in 10 stable PD patients within 2 weeks. One SPA was done
with the 3.86% low pH/high GDP solution, and the other with the 3.86% normal
pH/low GDP solution. The sequence of the two tests was randomized.
Results: Fluid transport parameters and glucose
absorption were not different between the two groups. No differences were
found for the mass transfer area coefficients (MTACs) of low molecular weight
solutes calculated over the whole dwell. However, MTAC urea in the first hour
of the dwell was higher in the test done with low pH/high GDP dialysate,
suggesting more peritoneal vasodilation. No difference was found in protein
clearances. Sodium sieving at multiple time points during the dwell was
similar with the two solutions.
Conclusion: The results obtained with the
glucose-containing normal pH/low GDP dialysis solution were similar to those
obtained with the glucose-containing low pH/high GDP dialysate in assessments
of peritoneal membrane function.
KEY WORDS: Assessment of peritoneal membrane function; biocompatible dialysis solution; solute transport; fluid kinetics; protein clearances; mesothelial cell mass marker CA125.
Received 18 April 2005; accepted 18 June 2007.
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