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Expanded hemodialysis as effective alternative to on-line hemodiafiltration: A randomized mid-term clinical trial. | LitMetric

AI Article Synopsis

  • Expanded hemodialysis (HDx) utilizes medium cut-off membranes to effectively clear middle molecules (MMs) and was compared to hemodiafiltration (HDF) in a study with patients already on HDF.
  • The study involved 21 patients switching to HDx and 22 continuing HDF over a 24-week follow-up, measuring reductions in MMs and clinical biomarkers.
  • HDx demonstrated greater reduction ratios for specific biomarkers and showed a tendency to lower the use of erythropoiesis-stimulating agents, suggesting it is a safe and effective alternative to HDF with potentially fewer resource needs.

Article Abstract

Expanded hemodialysis (HDx), using medium cut-off membrane, is a novel therapy that effectively clears middle molecules (MMs). We aimed to compare HDx to hemodiafiltration (HDF) in an open randomized clinical study. Patients currently on HDF (age 18-80 years; on HDF >3 months) were randomized to switch to HDx (N = 21) or continue HDF (N = 22) with a 24-week follow-up. Pre- to post-dialysis reduction ratios (RR) and changes in pre-dialysis levels over time were evaluated for MMs and clinical biomarkers. Use of erythropoiesis-stimulating agents (ESAs) was assessed. HDx showed greater RR for YKL-40 while RR appeared similar between groups for beta -microglobulin, FGF-23, and free light chains. Intradialytic changes in inflammatory biomarkers (IL-6, CRP, PTX3) did not differ between therapies. Changes from baseline to 12 and 24 weeks did not differ between groups for MMs, inflammatory markers, albumin, fibrinogen, hemoglobin, PTH, and phosphorus. Use of ESAs tended to decrease in HDx arm while remaining stable in HDF arm. HDx appeared safe with similar clinical effectiveness as HDF. With fewer requirements and resource needs, HDx provides an attractive alternative to HDF.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290668PMC
http://dx.doi.org/10.1111/1744-9987.13700DOI Listing

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