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Nephrol Dial Transplant (2000) 15: 74-78
© 2000 European Renal Association-European Dialysis and Transplant Association


Safety Aspects

Can sterile and pyrogen-free on-line substitution fluid be routinely delivered? A multicentric study on the microbiological safety of on-line haemodiafiltration

L. Vaslaki,1, A. Karátson2, P. Vörös3, L. Major4, F. Pethö5, E. Ladányi6, C. Weber7, R. Mitteregger8 and D. Falkenhagen8

1 Erzsébet Hospital Sopron, Sopron, Hungary 2 Dialysis Centre Pécs, Pecs, Hungary 3 Istvan Hospital Budapest, Budapest, Hungary 4 Dialysis Centre Esztergom, Esztergom, Hungary 5 Dialysis Center Salgótarján, Salgótarján, Hungary 6 Dialysis Centre Miskoic, Miskoic, Hungary 7 Fresenius Medical Care, Bad Homburg, Germany and 8 Centre for Biomedical Technology, Danube University Krems, Krems, Austria

Abstract

Background. Microbial contamination is characterized not only by the presence of bacteria, but also by high concentrations of biologically active by-products. They are potentially able to cross ultrafiltration and dialysis membranes and stimulate immunocompetent blood cells to synthesize cytokines. In turn, cytokine induction causes acute symptoms and has been incriminated in the long-term complications of haemodialysis patients. Infusion of large volumes of substitution fluids following ultrafiltration of microbially contaminated dialysis fluids may place patients on on-line therapies at particular risk.

Methods. In this study we evaluated 30 machines with a two-stage ultrafiltration system in routine clinical haemodiafiltration settings in six centres for 6 months. Microbiological safety was assessed monthly and at the last use of the filters by determining microbial counts, endotoxin concentration and cytokine-inducing activity.

Results. No pyrogenic episodes were observed during the study period. Double-filtration of standard dialysis fluid (range, <1–895 cfu/ml, 0.0028–4.6822 IU/ml) resulted in sterile substitution fluids with endotoxin concentrations well below the Ph.Eur. standard for haemofiltration solutions (range, 0.0014–0.0281 vs 0.25 IU/ml). Moreover, they did not differ from commercial haemofiltration solutions and depyrogenated saline. Likewise, there was no difference in the cytokine-inducing activity between the solutions tested. The high microbiological quality of the ultrafiltered dialysis fluid, which was in the same range as substitution fluid, translates into both the absence of cytokine induction by dialyser back-transport and a redundant safety mode of the on-line system by a second filtration step.

Conclusion. On-line HDF treatment can routinely be provided with ultra-pure dialysis fluids and sterile substitution fluids at pyrogen-free levels. The on-line preparation of substitution fluids thus can be considered microbiologically safe.

Notes

Correspondence and offprint requests to: Dr L. Vaslaki, Centre of Nephrology and Medical Ward, Erzsébet Hospital, Györi út 15, H-9400 Sopron, Hungary.


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H. Schiffl, S. M. Lang, D. Stratakis, and R. Fischer
Effects of ultrapure dialysis fluid on nutritional status and inflammatory parameters
Nephrol. Dial. Transplant., September 1, 2001; 16(9): 1863 - 1869.
[Abstract] [Full Text] [PDF]



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