|
|
||||||||
Icodextrin |
Lund University Hospital,1 Lund, Sweden; University of Toronto,2 Toronto, Canada; Akdeniz University,3 Antalya, Turkey
Correspondence to: D. Venturoli, Department of Nephrology, Lund University Hospital, S-22185 Lund, Sweden. Daniele.Venturoli{at}med.lu.se
Background: A recent study by Jeloka et al.
(Perit Dial Int 2006; 26:336–40) highlighted the high
variability in maximum ultrafiltered volume (UFmax) and the
corresponding dwell time (tmax) obtained using 7.5% icodextrin
solution. We aimed to pinpoint the possible sources of this phenomenon by
simulating the icodextrin ultrafiltration (UF) profiles according to the
three-pore model of peritoneal transport.
Method: The individual UF time courses observed in the
study by Jeloka et al. (n = 29) were first characterized by
linear and quadratic regression. We were then able to identify four main
patterns. These were then adapted to UF profiles generated by the three-pore
model by systematically altering the values of some model parameters, namely,
the mass transfer area coefficient (MTAC or PS) for icodextrin/glucose, the
peritoneal UF coefficient (LpS), the plasma colloid osmotic pressure gradient
(
), and the macromolecular clearance out of the peritoneal cavity
(ClLF).
Results: Modifications in the PS values caused only
marginal variations in UFmax and tmax, while more
significant changes were produced by altering LpS and ClLF.
However, far more evident was the importance of changes in 
. In
fact, lowering 
to 14 mmHg caused a steady increase in UF with 10
– 14 hour dwells. On the contrary, the UF profiles became nearly
"flat" when 
was increased to 30 mmHg. The parallel
shifts induced by altering icodextrin metabolite concentrations did not
markedly influence UFmax or tmax.
Conclusion: The UF pattern in icodextrin dwells seem to
be mainly determined by the plasma colloid osmotic pressure, while only
moderate changes can be seen with alterations in LpS and ClLF. The
result is not completely unexpected considering that icodextrin acts by
inducing a strong colloid osmotic gradient. A number of clinical studies would
be needed, however, in order to prove this hypothesis.
KEY WORDS: Three-pore model; macromolecular clearance; amylase; plasma protein concentration; colloid osmotic pressure.
Received 23 January 2008; accepted 22 September 2008.
This article has been cited by other articles:
|
|
M. Lambie, T. Stompor, and S. Davies UNDERSTANDING THE VARIABILITY IN ULTRAFILTRATION OBTAINED WITH ICODEXTRIN Perit. Dial. Int., July 1, 2009; 29(4): 407 - 411. [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |