@article{3670d162a76d4f888f40dc6c31430c87,
title = "Clinical Management of Hyperkalemia",
abstract = "Hyperkalemia is an electrolyte abnormality with potentially life-threatening consequences. Despite various guidelines, no universally accepted consensus exists on best practices for hyperkalemia monitoring, with variations in precise potassium (K+) concentration thresholds or for the management of acute or chronic hyperkalemia. Based on the available evidence, this review identifies several critical issues and unmet needs with regard to the management of hyperkalemia. Real-world studies are needed for a better understanding of the prevalence of hyperkalemia outside the clinical trial setting. There is a need to improve effective management of hyperkalemia, including classification and K+ monitoring, when to reinitiate previously discontinued renin-angiotensin-aldosterone system inhibitor (RAASi) therapy, and when to use oral K+-binding agents. Monitoring serum K+ should be individualized; however, increased frequency of monitoring should be considered for patients with chronic kidney disease, diabetes, heart failure, or a history of hyperkalemia and for those receiving RAASi therapy. Recent clinical studies suggest that the newer K+ binders (patiromer sorbitex calcium and sodium zirconium cyclosilicate) may facilitate optimization of RAASi therapy. Enhancing the knowledge of primary care physicians and internists with respect to the safety profiles of these newer K+ binders may increase confidence in managing patients with hyperkalemia. Lastly, the availability of newer K+-binding agents requires further study to establish whether stringent dietary K+ restrictions are needed in patients receiving K+-binder therapy. Individualized monitoring of serum K+ among patients with an increased risk of hyperkalemia and the use of newer K+-binding agents may allow for optimization of RAASi therapy and more effective management of hyperkalemia.",
author = "Palmer, {Biff F.} and Carrero, {Juan Jesus} and Clegg, {Deborah J.} and Colbert, {Gates B.} and Michael Emmett and Steven Fishbane and Hain, {Debra J.} and Edgar Lerma and Macaulay Onuigbo and Anjay Rastogi and Roger, {Simon D.} and Spinowitz, {Bruce S.} and Weir, {Matthew R.}",
note = "Funding Information: Potential Competing Interests: Dr Carrero has received advisory board fees and travel support from AstraZeneca and research grants and advisory board fees from Astellas Pharma Inc, Merck Sharp & Dohme Corp, and Vifor Pharma. Drs Colbert, Emmett, Hain, and Onuigbo have received advisory board fees from AstraZeneca. Dr Fishbane has received research funding and consulting fees from AstraZeneca . Dr Lerma has received research grants from ZS Pharma , Inc. Dr Rastogi has received advisory board and speakers bureau fees from AstraZeneca and Relypsa Inc and research grants from AstraZeneca . Dr Roger has received consulting and speakers bureau fees and travel support from AstraZeneca and Vifor Pharma . Dr Spinowitz has received grant support and personal fees from Akebia Therapeutics , Inc, AstraZeneca , FibroGen , Inc, and Reata Pharmaceuticals, Inc , and fees from Fresenius Medical Care. Dr Weir has received personal fees as scientific advisor for AbbVie Inc, Akebia Therapeutics, Inc, AstraZeneca, Bayer AG, Boehringer Ingelheim International GmbH, Boston Scientific Corporation, Janssen Pharmaceuticals, Inc, Merck Sharp & Dohme Corp, Relypsa Inc, and Vifor Pharma. The other authors report no competing interests. Funding Information: Grant Support: This work was supported in part by AstraZeneca.Potential Competing Interests: Dr Carrero has received advisory board fees and travel support from AstraZeneca and research grants and advisory board fees from Astellas Pharma Inc, Merck Sharp & Dohme Corp, and Vifor Pharma. Drs Colbert, Emmett, Hain, and Onuigbo have received advisory board fees from AstraZeneca. Dr Fishbane has received research funding and consulting fees from AstraZeneca. Dr Lerma has received research grants from ZS Pharma, Inc. Dr Rastogi has received advisory board and speakers bureau fees from AstraZeneca and Relypsa Inc and research grants from AstraZeneca. Dr Roger has received consulting and speakers bureau fees and travel support from AstraZeneca and Vifor Pharma. Dr Spinowitz has received grant support and personal fees from Akebia Therapeutics, Inc, AstraZeneca, FibroGen, Inc, and Reata Pharmaceuticals, Inc, and fees from Fresenius Medical Care. Dr Weir has received personal fees as scientific advisor for AbbVie Inc, Akebia Therapeutics, Inc, AstraZeneca, Bayer AG, Boehringer Ingelheim International GmbH, Boston Scientific Corporation, Janssen Pharmaceuticals, Inc, Merck Sharp & Dohme Corp, Relypsa Inc, and Vifor Pharma. The other authors report no competing interests.All named authors meet the International Committee of Medical Journal Editors criteria for authorship for this article and take responsibility for the integrity of the work as a whole. Medical writing support was provided by Sarah Greig, PhD (Auckland, New Zealand), and Meri Pozo, PhD (New York, NY), of inScience Communications, Springer Healthcare, in accordance with Good Publication Practice and funded by AstraZeneca. The authors had full editorial control of the submitted manuscript, reviewed and edited successive drafts, provided final approval of all content and submission of the manuscript, and are fully accountable for all aspects of the work. Publisher Copyright: {\textcopyright} 2020 Mayo Foundation for Medical Education and Research",
year = "2021",
month = mar,
doi = "10.1016/j.mayocp.2020.06.014",
language = "English (US)",
volume = "96",
pages = "744--762",
journal = "Mayo Clinic Proceedings",
issn = "0025-6196",
publisher = "Elsevier Science",
number = "3",
}