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Expanded hemodialysis as effective alternative to on‐line hemodiafiltration: A randomized mid‐term clinical trial
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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290668/ https://www.ncbi.nlm.nih.gov/pubmed/34125503 http://dx.doi.org/10.1111/1744-9987.13700 |
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author | Hadad‐Arrascue, Fernando Nilsson, Lars‐Göran Rivera, Angela S. Bernardo, Angelito A. Cabezuelo Romero, Juan B. |
author_facet | Hadad‐Arrascue, Fernando Nilsson, Lars‐Göran Rivera, Angela S. Bernardo, Angelito A. Cabezuelo Romero, Juan B. |
author_sort | Hadad‐Arrascue, Fernando |
collection | PubMed |
description | 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(2)‐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. |
format | Online Article Text |
id | pubmed-9290668 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-92906682022-07-20 Expanded hemodialysis as effective alternative to on‐line hemodiafiltration: A randomized mid‐term clinical trial Hadad‐Arrascue, Fernando Nilsson, Lars‐Göran Rivera, Angela S. Bernardo, Angelito A. Cabezuelo Romero, Juan B. Ther Apher Dial Original Articles 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(2)‐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. John Wiley & Sons Australia, Ltd 2021-06-29 2022-02 /pmc/articles/PMC9290668/ /pubmed/34125503 http://dx.doi.org/10.1111/1744-9987.13700 Text en © 2021 Baxter HealthCare Corporation. Therapeutic Apheresis and Dialysis published by John Wiley & Sons Australia, Ltd on behalf of International Society for Apheresis, Japanese Society for Apheresis, and Japanese Society for Dialysis Therapy. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Hadad‐Arrascue, Fernando Nilsson, Lars‐Göran Rivera, Angela S. Bernardo, Angelito A. Cabezuelo Romero, Juan B. Expanded hemodialysis as effective alternative to on‐line hemodiafiltration: A randomized mid‐term clinical trial |
title | Expanded hemodialysis as effective alternative to on‐line hemodiafiltration: A randomized mid‐term clinical trial |
title_full | Expanded hemodialysis as effective alternative to on‐line hemodiafiltration: A randomized mid‐term clinical trial |
title_fullStr | Expanded hemodialysis as effective alternative to on‐line hemodiafiltration: A randomized mid‐term clinical trial |
title_full_unstemmed | Expanded hemodialysis as effective alternative to on‐line hemodiafiltration: A randomized mid‐term clinical trial |
title_short | Expanded hemodialysis as effective alternative to on‐line hemodiafiltration: A randomized mid‐term clinical trial |
title_sort | expanded hemodialysis as effective alternative to on‐line hemodiafiltration: a randomized mid‐term clinical trial |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290668/ https://www.ncbi.nlm.nih.gov/pubmed/34125503 http://dx.doi.org/10.1111/1744-9987.13700 |
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