G. Woodrow et al., Comparison of icodextrin and glucose solutions for the daytime dwell in automated peritoneal dialysis, NEPH DIAL T, 14(6), 1999, pp. 1530-1535
Background. The sustained ultrafiltration achieved by icodextrin is more su
ited for the daytime dwell in automated peritoneal dialysis (APD) than gluc
ose solutions.
Methods. Seventeen patients receiving APD underwent assessment using three
different solutions for the daytime dwell: 2.27% glucose, 3.86% glucose and
7.5% icodextrin. Patients were then observed on icodextrin for a 6 month p
eriod.
Results. Daytime ultrafiltration was greater for 3.86% glucose (median 0.10
, IQR 0.01 to 0.321) P<0.01 and icodextrin (median 0.26, IQR 0.14 to 0.361)
P<0.001 than 2.27% glucose (median -0.19, IQR -0.54 to -0.081), with 3.86%
glucose and icodextrin not being significantly different. Positive ultrafi
ltration occurred in 3/17 patients with 2.27% glucose, 13/17 patients with
3.86% glucose and 16/17 patients with icodextrin (chi(2) P<0.0001). The dif
ference in ultrafiltration of icodextrin and 3.86% glucose correlated with
the 4h dialysate/plasma creatinine ratio in a PET test (r= 0.51, P<0.05). D
aytime Kt/V urea was greater for 3.86% glucose (median 0.27, IQR 0.20 to 0.
48 per week. P<0.01) and icodextrin (median 0.31, IQR 0.27 to 0.49 per week
, P<0.0001) than for 2.27% glucose (median 0.22. IQR 0.15 to 0.38 per week)
, with the difference between 3.86% glucose and icodextrin not reaching sta
tistical significance (P=0.06). Daytime creatinine clearance was greater fo
r 3.86% glucose (median 10.2, IQR 6.9 to 13.61/week/1.73 m(2), P<0.02) and
icodextrin (median 12.1, IQR 9.3 to 15.71/week/1.73 m(2), P<0.005) than for
2.27% glucose (median 8.8, IQR 4.9 to 11.91/week/1.73 m(2)). Daytime creat
inine clearance was greater for icodextrin than for 3.86% glucose (P<0.005)
. The effects of icodextrin were sustained for the 6 month observation peri
od.
Conclusions. Icodextrin produced enhanced ultrafiltration and clearances co
mpared with 2.27% glucose, without the exposure of the peritoncum to hypert
onic glucose solutions.