Long-term use and tolerability of irbesartan for control of hypertension

In this review, we discuss the pharmacological and clinical properties of irbesartan, a noncompetitive angiotensin II receptor type 1 antagonist, successfully used for more than a decade in the treatment of essential hypertension. Irbesartan exerts its antihypertensive effect through an inhibitory e...

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Main Authors: Forni, Valentina, Wuerzner, Grégoire, Pruijm, Menno, Burnier, Michel
Format: Online
Language:English
Published: Dove Medical Press 2011
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3172075/
id pubmed-3172075
recordtype oai_dc
spelling pubmed-31720752011-09-26 Long-term use and tolerability of irbesartan for control of hypertension Forni, Valentina Wuerzner, Grégoire Pruijm, Menno Burnier, Michel Review In this review, we discuss the pharmacological and clinical properties of irbesartan, a noncompetitive angiotensin II receptor type 1 antagonist, successfully used for more than a decade in the treatment of essential hypertension. Irbesartan exerts its antihypertensive effect through an inhibitory effect on the pressure response to angiotensin II. Irbesartan 150–300 mg once daily confers a lasting effect over 24 hours, and its antihypertensive efficacy is further enhanced by the coadministration of hydrochlorothiazide. Additionally and partially beyond its blood pressure-lowering effect, irbesartan reduces left ventricular hypertrophy, favors right atrial remodeling in atrial fibrillation, and increases the likelihood of maintenance of sinus rhythm after cardioversion in atrial fibrillation. In addition, the renoprotective effects of irbesartan are well documented in the early and later stages of renal disease in type 2 diabetics. Furthermore, both the therapeutic effectiveness and the placebo-like side effect profile contribute to a high adherence rate to the drug. Currently, irbesartan in monotherapy or combination therapy with hydrochlorothiazide represent a rationale pharmacologic approach for arterial hypertension and early-stage and late-stage diabetic nephropathy in hypertensive type II diabetics. Dove Medical Press 2011-04-18 /pmc/articles/PMC3172075/ /pubmed/21949635 http://dx.doi.org/10.2147/IBPC.S12211 Text en © 2011 Forni et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Forni, Valentina
Wuerzner, Grégoire
Pruijm, Menno
Burnier, Michel
spellingShingle Forni, Valentina
Wuerzner, Grégoire
Pruijm, Menno
Burnier, Michel
Long-term use and tolerability of irbesartan for control of hypertension
author_facet Forni, Valentina
Wuerzner, Grégoire
Pruijm, Menno
Burnier, Michel
author_sort Forni, Valentina
title Long-term use and tolerability of irbesartan for control of hypertension
title_short Long-term use and tolerability of irbesartan for control of hypertension
title_full Long-term use and tolerability of irbesartan for control of hypertension
title_fullStr Long-term use and tolerability of irbesartan for control of hypertension
title_full_unstemmed Long-term use and tolerability of irbesartan for control of hypertension
title_sort long-term use and tolerability of irbesartan for control of hypertension
description In this review, we discuss the pharmacological and clinical properties of irbesartan, a noncompetitive angiotensin II receptor type 1 antagonist, successfully used for more than a decade in the treatment of essential hypertension. Irbesartan exerts its antihypertensive effect through an inhibitory effect on the pressure response to angiotensin II. Irbesartan 150–300 mg once daily confers a lasting effect over 24 hours, and its antihypertensive efficacy is further enhanced by the coadministration of hydrochlorothiazide. Additionally and partially beyond its blood pressure-lowering effect, irbesartan reduces left ventricular hypertrophy, favors right atrial remodeling in atrial fibrillation, and increases the likelihood of maintenance of sinus rhythm after cardioversion in atrial fibrillation. In addition, the renoprotective effects of irbesartan are well documented in the early and later stages of renal disease in type 2 diabetics. Furthermore, both the therapeutic effectiveness and the placebo-like side effect profile contribute to a high adherence rate to the drug. Currently, irbesartan in monotherapy or combination therapy with hydrochlorothiazide represent a rationale pharmacologic approach for arterial hypertension and early-stage and late-stage diabetic nephropathy in hypertensive type II diabetics.
publisher Dove Medical Press
publishDate 2011
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3172075/
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