Background. Despite technological advances in dialysis equipment, the morbi
dity and quality of life of uraemic patients undergoing regular haemodialyt
ic treatment are still severely affected by acute intradialytic complicatio
ns possibly related to the treatment itself. Cardiovascular instability sti
ll affects > 30% of dialytic sessions and, although its pathogenesis is mul
tifactorial, dialysate sodium concentration land, consequently, intradialyt
ic sodium removal) is one of the main factors affecting intradialytic hypot
ension. Convective treatment modalities and so-called biocompatible membran
es increasingly are recognized as improving acute and particularly chronic
dialytic complications because a number of the pathways activated in patien
ts during dialysis with 'bioincompatible' membranes have the potential to p
roduce many side effects.
Methods. The main clinical studies are reviewed to highlight the advantages
of on-line monitoring and convective modalities on acute intradialytic sym
ptoms.
Results. The conductivity kinetic model has been shown to be a reliable and
inexpensive method of matching intradialytic sodium removal and interdialy
tic load. By applying this model to patients prone to dialysis hypotension,
a smaller reduction in intradialytic systolic blood pressure has been obse
rved, without any change in dialysate and reinfusate sodium concentrations
or dry body weight. Furthermore, a new model of haemodialysis potassium rem
oval based on a decreasing intradialytic potassium concentration and a cons
tant plasma-dialysate potassium gradient is capable of reducing the arrhyth
mogenic effect of standard haemodialysis. Despite the proven biological sup
eriority of biocompatible membranes, there is no definitive evidence that m
embrane biocompatibility and/or flux lead to a decrease in acute intradialy
tic clinical symptoms.
Conclusions. On-line monitoring of intradialytic sodium removal and the pot
assium gradient is capable of reducing intradialytic hypotension and the ar
rhythmogenic effect of haemodialysis, and thus having a considerable clinic
al impact on acute intradialysis complications. As far as the effects of bi
ocompatibility and/or flux on the incidence of acute intradialytic clinical
symptoms are concerned, further trials involving a sicker patient populati
on with higher prevalence of intradialytic hypotension are needed in order
to achieve statistical power.