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IHDIP: a controlled randomized trial to assess the security and effectiveness of the incremental hemodialysis in incident patients
BACKGROUND: Most people who make the transition to renal replacement therapy (RRT) are treated with a fixed dose thrice-weekly hemodialysis réegimen, without considering their residual kidney function (RKF). Recent papers inform us that incremental hemodialysis is associated with preservation of RKF...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6325813/ https://www.ncbi.nlm.nih.gov/pubmed/30626347 http://dx.doi.org/10.1186/s12882-018-1189-6 |
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author | Deira, Javier Suárez, Miguel A. López, Francisca García-Cabrera, Emilio Gascón, Antonio Torregrosa, Eduardo García, Giannina E. Huertas, Jorge de la Flor, Jose C. Puello, Suleya Gómez-Raja, Jonathan Grande, Jesús Lerma, José L. Corradino, Carlos Musso, Carlos Ramos, Manuel Martín, Jesús Basile, Carlo Casino, Francesco G. |
author_facet | Deira, Javier Suárez, Miguel A. López, Francisca García-Cabrera, Emilio Gascón, Antonio Torregrosa, Eduardo García, Giannina E. Huertas, Jorge de la Flor, Jose C. Puello, Suleya Gómez-Raja, Jonathan Grande, Jesús Lerma, José L. Corradino, Carlos Musso, Carlos Ramos, Manuel Martín, Jesús Basile, Carlo Casino, Francesco G. |
author_sort | Deira, Javier |
collection | PubMed |
description | BACKGROUND: Most people who make the transition to renal replacement therapy (RRT) are treated with a fixed dose thrice-weekly hemodialysis réegimen, without considering their residual kidney function (RKF). Recent papers inform us that incremental hemodialysis is associated with preservation of RKF, whenever compared with conventional hemodialysis. The objective of the present controlled randomized trial (RCT) is to determine if start HD with one sessions per week (1-Wk/HD), it is associated with better patient survival and other safety parameters. METHODS/DESIGN: IHDIP is a multicenter RCT experimental open trial. It is randomized in a 1:1 ratio and controlled through usual clinical practice, with a low intervention level and non-commercial. It includes 152 incident patients older than 18 years, with a RRF of ≥4 ml/min/1.73 m2, measured by renal clearance of urea (KrU). The intervention group includes 76 patients who will start with incremental HD (1-Wk/HD). The control group includes 76 patients who will start with thrice-weekly hemodialysis régimen. The primary outcome is assessing the survival rate, while the secondary outcomes are the morbidity rate, the clinical parameters, the quality of life and the efficiency. DISCUSSION: This study will enable to know the number of sessions a patient should receive when starting HD, depending on his RRF. The potentially important clinical and financial implications of incremental hemodialysis warrant this RCT. TRIAL REGISTRATION: U.S. National Institutes of Health, ClinicalTrials.gov. Number: NCT03239808, completed 13/04/2017. Sponsor: Foundation for Training and Research of Health Professionals of Extremadura. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12882-018-1189-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6325813 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63258132019-01-11 IHDIP: a controlled randomized trial to assess the security and effectiveness of the incremental hemodialysis in incident patients Deira, Javier Suárez, Miguel A. López, Francisca García-Cabrera, Emilio Gascón, Antonio Torregrosa, Eduardo García, Giannina E. Huertas, Jorge de la Flor, Jose C. Puello, Suleya Gómez-Raja, Jonathan Grande, Jesús Lerma, José L. Corradino, Carlos Musso, Carlos Ramos, Manuel Martín, Jesús Basile, Carlo Casino, Francesco G. BMC Nephrol Study Protocol BACKGROUND: Most people who make the transition to renal replacement therapy (RRT) are treated with a fixed dose thrice-weekly hemodialysis réegimen, without considering their residual kidney function (RKF). Recent papers inform us that incremental hemodialysis is associated with preservation of RKF, whenever compared with conventional hemodialysis. The objective of the present controlled randomized trial (RCT) is to determine if start HD with one sessions per week (1-Wk/HD), it is associated with better patient survival and other safety parameters. METHODS/DESIGN: IHDIP is a multicenter RCT experimental open trial. It is randomized in a 1:1 ratio and controlled through usual clinical practice, with a low intervention level and non-commercial. It includes 152 incident patients older than 18 years, with a RRF of ≥4 ml/min/1.73 m2, measured by renal clearance of urea (KrU). The intervention group includes 76 patients who will start with incremental HD (1-Wk/HD). The control group includes 76 patients who will start with thrice-weekly hemodialysis régimen. The primary outcome is assessing the survival rate, while the secondary outcomes are the morbidity rate, the clinical parameters, the quality of life and the efficiency. DISCUSSION: This study will enable to know the number of sessions a patient should receive when starting HD, depending on his RRF. The potentially important clinical and financial implications of incremental hemodialysis warrant this RCT. TRIAL REGISTRATION: U.S. National Institutes of Health, ClinicalTrials.gov. Number: NCT03239808, completed 13/04/2017. Sponsor: Foundation for Training and Research of Health Professionals of Extremadura. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12882-018-1189-6) contains supplementary material, which is available to authorized users. BioMed Central 2019-01-09 /pmc/articles/PMC6325813/ /pubmed/30626347 http://dx.doi.org/10.1186/s12882-018-1189-6 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Study Protocol Deira, Javier Suárez, Miguel A. López, Francisca García-Cabrera, Emilio Gascón, Antonio Torregrosa, Eduardo García, Giannina E. Huertas, Jorge de la Flor, Jose C. Puello, Suleya Gómez-Raja, Jonathan Grande, Jesús Lerma, José L. Corradino, Carlos Musso, Carlos Ramos, Manuel Martín, Jesús Basile, Carlo Casino, Francesco G. IHDIP: a controlled randomized trial to assess the security and effectiveness of the incremental hemodialysis in incident patients |
title | IHDIP: a controlled randomized trial to assess the security and effectiveness of the incremental hemodialysis in incident patients |
title_full | IHDIP: a controlled randomized trial to assess the security and effectiveness of the incremental hemodialysis in incident patients |
title_fullStr | IHDIP: a controlled randomized trial to assess the security and effectiveness of the incremental hemodialysis in incident patients |
title_full_unstemmed | IHDIP: a controlled randomized trial to assess the security and effectiveness of the incremental hemodialysis in incident patients |
title_short | IHDIP: a controlled randomized trial to assess the security and effectiveness of the incremental hemodialysis in incident patients |
title_sort | ihdip: a controlled randomized trial to assess the security and effectiveness of the incremental hemodialysis in incident patients |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6325813/ https://www.ncbi.nlm.nih.gov/pubmed/30626347 http://dx.doi.org/10.1186/s12882-018-1189-6 |
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