ONLINE HEMODIAFILTRATION WITH PRE-DILUTION AND POSTDILUTION - A COMPARISON OF EFFICACY

Since the introduction of on-line substituate preparation, high substi tuate rates (Q(s)) in pre- and postdilution for hemodiafiltration (HDF ) procedures can be realized. During postdilution HDF (POD-HDF) and ad ditional convective removal is possible, but in vivo Q(s) is limited t o approx. 1/3Q(b) (bloodflow). With predilution HDF (PRD-HDF) higher Q (s) and therefore high convective transport rates by ultrafiltration c an be reached. On the other hand the blood concentration is diminished by predilution. Further decrease of the diffusive transport is caused by reduced dialysate flow Q(d) due to separation of the substituate f rom the dialysate (Fresenius 4008 On-Line HDF; Gambro AK100 Ultra). Th e theoretical description of the combined diffusive-convective transpo rt is limited to I-dimensional models and small UP-rates. Therefore fo r practical and theoretical purposes the assessment of the efficacy of on-line PRD-HDF and POD-HDF in different molecular weight ranges is d esirable. By means of in vitro experiments the effective clearances K- eff of hemodialysis (HD dialyzer: Fresenius F60) for urea, creatinine, vitamin B12 and inulin were compared with measured and theoretical K- eff of POD- and PRD-HDF: The theoretical expectation is confirmed that K-eff for small molecular weight substances decreases slightly with P RD-HDF and increases for larger molecules. In the case of POD-HDF K-ef f for small molecular weight substances increases slightly and strongl y for larger molecules. in vivo experiments were performed to measure the real substance removal from patient's blood and to figure out the impact of dialysate flow (collection of the used dialysate during the ii treatment hour and concentration measurements for urea, creatinine, phosphate, beta(2)-MG). The results show that the substraction of Q(s ) from Q(d) reduces K-eff for urea, creatinine and phosphate but not f or beta(2)-MG. PRD-HDF with Q(d) = 500 ml/min is significantly less ef fective for small molecules than HD. There is no significant differenc e of K-eff for urea, creatinine, phosphate during HD and PRD-HDF with Q(d) = 800 ml/min, but a significant increase of 10-15% for POD-HDF. K -eff for beta(2)-MG increases by 75% for PRD-HDF and 95% for POD-HDF c ompared with HD (Q(d) = 500 ml/min).