Background. Highly permeable biocompatible dialysis membranes may postpone
the development of AB-amyloidosis, but the relative contribution of enhance
d flux or reduced inflammation by highly biocompatible membranes and steril
e dialysis fluid remains unknown.
Methods. In this retrospective investigation, 89 patients with end-stage re
nal disease maintained on regular haemodialysis for at least 10 years and t
reated with one type of dialysis membrane exclusively were selected for ana
lysis. They were divided into three groups: low-flux, bioincompatible cellu
lose (I), low-flux, intermediately biocompatible polysulphone or PMMA (II),
or high-flux, highly biocompatible polys ulphone or AN69 (III). In additio
n, the patients were analysed according to the microbiological quality of t
he dialysis fluid, which had been tested regularly and was classified eithe
r as standard or as intermittently contaminated. The clinical manifestation
s indicative of AB-amyloidosis, namely, carpal tunnel syndrome, arthropathy
and bone cysts, were diagnosed after recruitment.
Results. Clinical symptoms were most pronounced in group I, intermediate in
group II, and lowest in group III. Patients treated with intermittently co
ntaminated dialysis fluid showed a higher prevalence of AB-amyloidosis than
patients with less contaminated dialysis fluid. Logistic regression analys
is demonstrated that the flux characteristics of the dialyser and the micro
biological quality of the dialysis fluid as well as the biocompatibility of
the dialyser were independent determinants of AB-amyloidosis.
Conclusion. It would be prudent clinical practice to employ high-flux bioco
mpatible membranes in conjunction with ultrapure dialysis fluid for the tre
atment of end-stage renal disease patients who need to remain on long-term
haemodialysis.