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Clinical Sciences |
Manchester Institute of Nephrology and Transplantation, Manchester Royal Infirmary, Manchester, United Kingdom
Correspondence to: A. Hutchison, Renal Department, Manchester Royal Infirmary, Oxford Road, Manchester, M13 9WL, United Kingdom. alastair.hutchison{at}cmft.nhs.uk
Background: Calcium and magnesium balance in continuous
ambulatory peritoneal dialysis (CAPD) has been extensively studied with
several of the different formulations of fluid available. Calcium and
magnesium balance in automated PD (APD) is less well studied and the effect on
Ca and Mg flux is unknown. Data on glucose polymer solutions are also lacking.
This prospective observational study was undertaken to examine mass transfer
of Ca and Mg in APD patients.
Methods: 12 patients on APD were studied for two
24-hour periods using, alternately, 1.75 mmol/L and 1.25 mmol/L Ca (Dianeal
PD1 and Dianeal PD4; Baxter Healthcare, Newbury, UK) 1.36% glucose-based
dialysis fluid for the 9-hour overnight dialysis, followed by a 15-hour
daytime dwell of glucose polymer-based fluid (icodextrin). Serum ionized Ca,
serum Mg, and dialysate Ca and Mg concentrations were measured at the
beginning and end of each period. Mass transfer was calculated as millimoles
per exchange.
Results: During rapid overnight exchanges with Dianeal
PD1 and PD4, mass transfer of Mg and Ca did not show significant correlations
with serum levels when using PD1 fluid; however, mass transfer of Mg, but not
Ca, was significantly correlated to serum levels when using PD4 fluid. During
the long dwell with icodextrin, dialysate drain volume was the most
significant factor determining the flux of both Ca and Mg.
Conclusion: Mass transfer of Ca and Mg in APD patients
using conventional dialysis fluid was not related to drain volume in this
study, which differs to studies in CAPD. Flux of Ca and Mg during icodextrin
use was found to be dependent on ultrafiltration rate and not dialysate or
serum concentration.
KEY WORDS: Calcium; magnesium; automated peritoneal dialysis; mass transfer; chronic kidney disease.
Received 4 April 2007; accepted 22 September 2008.
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