Aldosterone Receptor Antagonists: Focus on Eplerenone
Despite the development of hypertension treatment guidelines, blood pressure control in the general population remains inadequate, indicating the need for ongoing re‐evaluation of treatment strategies to further improve blood pressure control. Hypertension results from alterations in cardiac output...
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Published in | Progress in cardiovascular nursing Vol. 18; no. 1; pp. 54 - 59 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Three Parklands Drive, Darien, CT 06820-3652
CHF, Inc
01.01.2003
LeJacq Communications, Inc |
Subjects | |
Online Access | Get full text |
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Summary: | Despite the development of hypertension treatment guidelines, blood pressure control in the general population remains inadequate, indicating the need for ongoing re‐evaluation of treatment strategies to further improve blood pressure control. Hypertension results from alterations in cardiac output and/or peripheral resistance. The renin‐angiotensin‐aldosterone system may be responsible, at least in part, for these alterations. Despite pharmacologic intervention with angiotensin‐converting enzyme inhibitors and angiotensin type‐1 receptor antagonists, aldosterone continues to be produced. Therapeutic modalities for treating hypertension directed toward antagonizing aldosterone might more effectively control blood pressure. Eplerenone, a new selective aldosterone receptor antagonist, recently received approval from the US Food and Drug Administration for the treatment of hypertension, either alone or in combination with other antihypertensive agents. The objective of this review is to summarize the renin‐angiotensin‐aldosterone system, emphasizing the role for aldosterone antagonism in the management of hypertension, with a focus on eplerenone. |
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Bibliography: | istex:A37A5DB2447BF33C5789035ED40CA0C165867F79 ark:/67375/WNG-3ZCSFHRP-2 ArticleID:PCV1936 ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 |
ISSN: | 0889-7204 1751-7117 |
DOI: | 10.1111/j.0889-7204.2003.01936.x |