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Real-world effectiveness of valsartan on hypertension and total cardiovascular risk: review and implications of a translational research program

The pharmacological efficacy of various monotherapy, single pill, and combination therapies of the angiotensin II receptor blocker valsartan have been established, mainly through randomized controlled trials that used similar methodological and statistical platforms and thus enabled synthesis of evi...

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Autores principales: Abraham, Ivo, MacDonald, Karen, Hermans, Christine, Aerts, Ann, Lee, Christopher, Brié, Heidi, Vancayzeele, Stefaan
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3072745/
https://www.ncbi.nlm.nih.gov/pubmed/21490947
http://dx.doi.org/10.2147/VHRM.S9434
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author Abraham, Ivo
MacDonald, Karen
Hermans, Christine
Aerts, Ann
Lee, Christopher
Brié, Heidi
Vancayzeele, Stefaan
author_facet Abraham, Ivo
MacDonald, Karen
Hermans, Christine
Aerts, Ann
Lee, Christopher
Brié, Heidi
Vancayzeele, Stefaan
author_sort Abraham, Ivo
collection PubMed
description The pharmacological efficacy of various monotherapy, single pill, and combination therapies of the angiotensin II receptor blocker valsartan have been established, mainly through randomized controlled trials that used similar methodological and statistical platforms and thus enabled synthesis of evidence. The real world effectiveness of valsartan has been studied extensively, but the relative lack of scientific and technical congruence of these studies render synthesis virtually impossible. To date, all have focused on blood pressure outcomes, despite evidence-based calls to grade antihypertensive treatment to patients’ total cardiovascular risk. We review a T3 translational research program of seven studies involving valsartan monotherapy as well as single and separate pill combinations, and the determinants and effect on blood pressure and total cardiovascular risk outcomes. All seven studies examined not only the impact of valsartan-based regimens on blood pressure values and control, but also, within a statistical hierarchical approach, the physician- and patient-related determinants of these blood pressure outcomes. Two studies also investigated the determinants and outcomes of valsartan-based treatment on total cardiovascular risk – among the first studies to use this risk coefficient as an outcome rather than only a determinant. These seven studies included a total of 19,533 patients, contributed by 3434 physician-investigators in Belgium – a country particularly well-suited for observational effectiveness studies because of demographics and epidemiology. Each study used the same methodological and statistical platform. We summarize the impact of various valsartan regimens on such outcomes as blood pressure values and control, change in total cardiovascular risk, and reduction in risk by at least one category. We also review the results of statistical multilevel and logistic modeling of physician- and patient-related determinants on these outcomes, including the proportion of variance attributable to a physician class effect before patients enter the equation. In its different formulations, valsartan has major real-world benefits in lowering blood pressure and total cardiovascular risk within a 90-day period. It is essential to understand the physician- and patient-related determinants of blood pressure and total cardiovascular risk outcomes associated with valsartan treatment. Antihypertensive research should expand its historical focus on lowering blood pressure with an emphasis on lowering total cardiovascular research.
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spelling pubmed-30727452011-04-13 Real-world effectiveness of valsartan on hypertension and total cardiovascular risk: review and implications of a translational research program Abraham, Ivo MacDonald, Karen Hermans, Christine Aerts, Ann Lee, Christopher Brié, Heidi Vancayzeele, Stefaan Vasc Health Risk Manag Review The pharmacological efficacy of various monotherapy, single pill, and combination therapies of the angiotensin II receptor blocker valsartan have been established, mainly through randomized controlled trials that used similar methodological and statistical platforms and thus enabled synthesis of evidence. The real world effectiveness of valsartan has been studied extensively, but the relative lack of scientific and technical congruence of these studies render synthesis virtually impossible. To date, all have focused on blood pressure outcomes, despite evidence-based calls to grade antihypertensive treatment to patients’ total cardiovascular risk. We review a T3 translational research program of seven studies involving valsartan monotherapy as well as single and separate pill combinations, and the determinants and effect on blood pressure and total cardiovascular risk outcomes. All seven studies examined not only the impact of valsartan-based regimens on blood pressure values and control, but also, within a statistical hierarchical approach, the physician- and patient-related determinants of these blood pressure outcomes. Two studies also investigated the determinants and outcomes of valsartan-based treatment on total cardiovascular risk – among the first studies to use this risk coefficient as an outcome rather than only a determinant. These seven studies included a total of 19,533 patients, contributed by 3434 physician-investigators in Belgium – a country particularly well-suited for observational effectiveness studies because of demographics and epidemiology. Each study used the same methodological and statistical platform. We summarize the impact of various valsartan regimens on such outcomes as blood pressure values and control, change in total cardiovascular risk, and reduction in risk by at least one category. We also review the results of statistical multilevel and logistic modeling of physician- and patient-related determinants on these outcomes, including the proportion of variance attributable to a physician class effect before patients enter the equation. In its different formulations, valsartan has major real-world benefits in lowering blood pressure and total cardiovascular risk within a 90-day period. It is essential to understand the physician- and patient-related determinants of blood pressure and total cardiovascular risk outcomes associated with valsartan treatment. Antihypertensive research should expand its historical focus on lowering blood pressure with an emphasis on lowering total cardiovascular research. Dove Medical Press 2011 2011-03-31 /pmc/articles/PMC3072745/ /pubmed/21490947 http://dx.doi.org/10.2147/VHRM.S9434 Text en © 2011 Abraham 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.
spellingShingle Review
Abraham, Ivo
MacDonald, Karen
Hermans, Christine
Aerts, Ann
Lee, Christopher
Brié, Heidi
Vancayzeele, Stefaan
Real-world effectiveness of valsartan on hypertension and total cardiovascular risk: review and implications of a translational research program
title Real-world effectiveness of valsartan on hypertension and total cardiovascular risk: review and implications of a translational research program
title_full Real-world effectiveness of valsartan on hypertension and total cardiovascular risk: review and implications of a translational research program
title_fullStr Real-world effectiveness of valsartan on hypertension and total cardiovascular risk: review and implications of a translational research program
title_full_unstemmed Real-world effectiveness of valsartan on hypertension and total cardiovascular risk: review and implications of a translational research program
title_short Real-world effectiveness of valsartan on hypertension and total cardiovascular risk: review and implications of a translational research program
title_sort real-world effectiveness of valsartan on hypertension and total cardiovascular risk: review and implications of a translational research program
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3072745/
https://www.ncbi.nlm.nih.gov/pubmed/21490947
http://dx.doi.org/10.2147/VHRM.S9434
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