Course of Hyperkalemia in Patients on Hemodialysis.


Journal

International journal of nephrology
ISSN: 2090-214X
Titre abrégé: Int J Nephrol
Pays: United States
ID NLM: 101546753

Informations de publication

Date de publication:
2022
Historique:
received: 18 11 2021
revised: 29 03 2022
accepted: 07 04 2022
entrez: 9 5 2022
pubmed: 10 5 2022
medline: 10 5 2022
Statut: epublish

Résumé

Evidence of longitudinal serum potassium (sK These post hoc analyses of the placebo arm of the phase 3b DIALIZE study (NCT03303521) explored the course of hyperkalemia in hemodialysis patients receiving placebo. In DIALIZE, 196 patients receiving hemodialysis three times weekly were randomized to placebo or sodium zirconium cyclosilicate 5 g starting dose once daily on nondialysis days for 8 weeks. In these post hoc analyses of placebo patients overall ( In placebo patients, the mean predialysis sK Patients receiving placebo and hemodialysis maintained high predialysis sK

Sections du résumé

Background UNASSIGNED
Evidence of longitudinal serum potassium (sK
Objective UNASSIGNED
These post hoc analyses of the placebo arm of the phase 3b DIALIZE study (NCT03303521) explored the course of hyperkalemia in hemodialysis patients receiving placebo.
Methods UNASSIGNED
In DIALIZE, 196 patients receiving hemodialysis three times weekly were randomized to placebo or sodium zirconium cyclosilicate 5 g starting dose once daily on nondialysis days for 8 weeks. In these post hoc analyses of placebo patients overall (
Results UNASSIGNED
In placebo patients, the mean predialysis sK
Conclusions UNASSIGNED
Patients receiving placebo and hemodialysis maintained high predialysis sK

Identifiants

pubmed: 35531468
doi: 10.1155/2022/6304571
pmc: PMC9071981
doi:

Types de publication

Journal Article

Langues

eng

Pagination

6304571

Informations de copyright

Copyright © 2022 Bruce Spinowitz et al.

Déclaration de conflit d'intérêts

BS received research grants, lecture fees, and/or consulting fees from AstraZeneca, Akebia, Reata Pharmaceuticals, and Fresenius Medical Care. SF received research support and consulting fees from AstraZeneca. MFu received consulting fees and lecture fees from AstraZeneca Japan. MFo received travel support from Amgen and AstraZeneca and is an advisory board member for AstraZeneca. NG is an employee of AstraZeneca. AR received research or travel support from, and/or is a speaker, consultant, or advisory board member for AstraZeneca, Vifor Pharma, Fresenius Medical Care, Sanofi, Kadmon, Amag, Otsuka, Genzyme, GlaxoSmithKline, Omeros, Janssen, Reata Pharmaceuticals, Ironwood, and Amgen.

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Auteurs

Bruce Spinowitz (B)

Department of Medicine, NewYork-Presbyterian Queens, Queens, NY, USA.

Steven Fishbane (S)

Department of Medicine, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Great Neck, NY, USA.

Masafumi Fukagawa (M)

Division of Nephrology, Endocrinology and Metabolism, Department of Internal Medicine, Tokai University School of Medicine, Isehara, Japan.

Martin Ford (M)

Department of Renal Medicine, King's College Hospital NHS Trust, London, UK.
Faculty of Life Sciences and Medicine, King's College London, London, UK.

Nicolas Guzman (N)

Global Medicines Development, AstraZeneca BioPharmaceuticals Research and Development, Gaithersburg, MD, USA.

Anjay Rastogi (A)

UCLA CORE Kidney Program, University of California Los Angeles, Los Angeles, CA, USA.

Classifications MeSH