| Literature DB >> 27140336 |
Faiez Zannad1, Patrick Rossignol2, Wendy Gattis Stough3, Murray Epstein4, Maria de Los Angeles Alonso Garcia5, George L Bakris6, Javed Butler7, Mikhail Kosiborod8, Lance Berman9, Alexandre Mebazaa10, Henrik S Rasmussen11, Luis M Ruilope12, Norman Stockbridge13, Aliza Thompson13, Janet Wittes14, Bertram Pitt15.
Abstract
Hyperkalemia is a common clinical problem, especially in patients with chronic kidney disease, diabetes mellitus, or heart failure. Treatment with renin angiotensin aldosterone system inhibitors exacerbates the risk of hyperkalemia in these patients. Concern about hyperkalemia can result in the failure to initiate, suboptimal dosing, or discontinuation of renin angiotensin aldosterone system inhibitor therapy in patients; effective treatments for hyperkalemia might mitigate such undertreatment. New treatments for hyperkalemia in development may offer better efficacy, tolerability and safety profiles than do existing approved treatments. These compounds might enable more eligible patients to receive renin angiotensin aldosterone system inhibitor therapy or to receive renin angiotensin aldosterone system inhibitors at target doses. The evidence needed to support a treatment claim (reduction in serum potassium) differs from that needed to support a prevention claim (preventing hyperkalemia to allow renin angiotensin aldosterone system inhibitor treatment). Thus, several issues related to clinical trial design and drug development need to be considered. This paper summarizes and expands upon a discussion at the Global Cardiovascular Clinical Trialists 2014 Forum and examines methodologic considerations for trials of new potassium binders for the prevention and management of hyperkalemia in patients with renin angiotensin aldosterone system inhibitor indications.Entities:
Keywords: Chronic; Clinical trials as topic; Heart failure; Hyperkalemia; Polymers; Renal insufficiency; Renin–angiotensin system
Mesh:
Substances:
Year: 2016 PMID: 27140336 DOI: 10.1016/j.ijcard.2016.04.127
Source DB: PubMed Journal: Int J Cardiol ISSN: 0167-5273 Impact factor: 4.164