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Dialyzer membrane type and reuse practice influence polymorphonuclear leukocyte function in hemodialysis patients
Madhumathi Rao1, Daqing Guo, Bertrand L Jaber
1Division of Nephrology, Tufts-New England Medical Center, Boston, Massachusetts 02111, USA.
Kidney International
|January 14, 2004
Summary
Dialyzer membrane type and reuse impact polymorphonuclear leukocyte (PMNL) function in hemodialysis (HD) patients. These factors influence reactive oxygen species (ROS) production, potentially affecting HD-associated morbidity.
Area of Science:
- Nephrology
- Immunology
- Biomedical Engineering
Background:
- Polymorphonuclear leukocyte (PMNL) production of reactive oxygen species (ROS) is linked to hemodialysis (HD)-associated morbidity.
- The specific effects of dialyzer membrane type and reuse on PMNL function remain incompletely understood.
Purpose of the Study:
- To investigate the association between patient and dialysis-related factors and PMNL function in regular HD patients.
- To determine how dialyzer membrane material and reuse practices influence PMNL oxidative response.
Main Methods:
- Cross-sectional study of HD patients at enrollment in the Hemodialysis (HEMO) Study.
- Assessed PMNL function via PMA- and N-formyl methionyl-leucyl-phenylalanine (fMLP)-induced respiratory burst and phagocytic activity against Staphylococcus aureus.
Main Results:
- Polysulfone (PS) and cuprophane (CU) membranes showed higher PMA-induced respiratory burst than substituted cellulose (CA/CT) membranes, irrespective of reuse.
- Dialyzer reuse with bleach was linked to increased PMA-induced PMNL superoxide production; renalin as a germicide also increased phagocytosis.
- Longer duration on HD correlated inversely with PMA-induced PMNL superoxide response; poorer functional status correlated with weaker fMLP response.
Conclusions:
- Dialyzer membrane type and reuse significantly influence PMNL oxidative response in HD patients.
- Further prospective studies are needed to evaluate the clinical implications of these findings on patient morbidity.