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New strategies and therapies for the prevention of heart failure in high‐risk patients

Despite declines in total cardiovascular mortality rates in the United States, heart failure (HF) mortality rates as well as hospitalizations and readmissions have increased in the past decade. Increases have been relatively higher among young and middle‐aged adults (<65 years). Therefore, identi...

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Autores principales: Hammond, Michael M., Everitt, Ian K., Khan, Sadiya S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9254668/
https://www.ncbi.nlm.nih.gov/pubmed/35789013
http://dx.doi.org/10.1002/clc.23839
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author Hammond, Michael M.
Everitt, Ian K.
Khan, Sadiya S.
author_facet Hammond, Michael M.
Everitt, Ian K.
Khan, Sadiya S.
author_sort Hammond, Michael M.
collection PubMed
description Despite declines in total cardiovascular mortality rates in the United States, heart failure (HF) mortality rates as well as hospitalizations and readmissions have increased in the past decade. Increases have been relatively higher among young and middle‐aged adults (<65 years). Therefore, identification of individuals HF at‐risk (Stage A) or with pre‐HF (Stage B) before the onset of overt clinical signs and symptoms (Stage C) is urgently needed. Multivariate risk models (e.g., Pooled Cohort Equations to Prevent Heart Failure [PCP‐HF]) have been externally validated in diverse populations and endorsed by the 2022 HF Guidelines to apply a risk‐based framework for the prevention of HF. However, traditional risk factors included in the PCP‐HF model only account for half of an individual's lifetime risk of HF; novel risk factors (e.g., adverse pregnancy outcomes, impaired lung health, COVID‐19) are emerging as important risk‐enhancing factors that need to be accounted for in personalized approaches to prevention. In addition to determining the role of novel risk‐enhancing factors, integration of social determinants of health (SDoH) in identifying and addressing HF risk is needed to transform the current clinical paradigm for the prevention of HF. Comprehensive strategies to prevent the progression of HF must incorporate pharmacotherapies (e.g., sodium glucose co‐transporter‐2 inhibitors that have also been termed the “statins” of HF prevention), intensive blood pressure lowering, and heart‐healthy behaviors. Future directions include investigation of novel prediction models leveraging machine learning, integration of risk‐enhancing factors and SDoH, and equitable approaches to interventions for risk‐based prevention of HF.
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spelling pubmed-92546682022-07-08 New strategies and therapies for the prevention of heart failure in high‐risk patients Hammond, Michael M. Everitt, Ian K. Khan, Sadiya S. Clin Cardiol Publication of this special issue was made possible by AstraZeneca. Despite declines in total cardiovascular mortality rates in the United States, heart failure (HF) mortality rates as well as hospitalizations and readmissions have increased in the past decade. Increases have been relatively higher among young and middle‐aged adults (<65 years). Therefore, identification of individuals HF at‐risk (Stage A) or with pre‐HF (Stage B) before the onset of overt clinical signs and symptoms (Stage C) is urgently needed. Multivariate risk models (e.g., Pooled Cohort Equations to Prevent Heart Failure [PCP‐HF]) have been externally validated in diverse populations and endorsed by the 2022 HF Guidelines to apply a risk‐based framework for the prevention of HF. However, traditional risk factors included in the PCP‐HF model only account for half of an individual's lifetime risk of HF; novel risk factors (e.g., adverse pregnancy outcomes, impaired lung health, COVID‐19) are emerging as important risk‐enhancing factors that need to be accounted for in personalized approaches to prevention. In addition to determining the role of novel risk‐enhancing factors, integration of social determinants of health (SDoH) in identifying and addressing HF risk is needed to transform the current clinical paradigm for the prevention of HF. Comprehensive strategies to prevent the progression of HF must incorporate pharmacotherapies (e.g., sodium glucose co‐transporter‐2 inhibitors that have also been termed the “statins” of HF prevention), intensive blood pressure lowering, and heart‐healthy behaviors. Future directions include investigation of novel prediction models leveraging machine learning, integration of risk‐enhancing factors and SDoH, and equitable approaches to interventions for risk‐based prevention of HF. John Wiley and Sons Inc. 2022-07-05 /pmc/articles/PMC9254668/ /pubmed/35789013 http://dx.doi.org/10.1002/clc.23839 Text en © 2022 The Authors. Clinical Cardiology published by Wiley Periodicals, LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Publication of this special issue was made possible by AstraZeneca.
Hammond, Michael M.
Everitt, Ian K.
Khan, Sadiya S.
New strategies and therapies for the prevention of heart failure in high‐risk patients
title New strategies and therapies for the prevention of heart failure in high‐risk patients
title_full New strategies and therapies for the prevention of heart failure in high‐risk patients
title_fullStr New strategies and therapies for the prevention of heart failure in high‐risk patients
title_full_unstemmed New strategies and therapies for the prevention of heart failure in high‐risk patients
title_short New strategies and therapies for the prevention of heart failure in high‐risk patients
title_sort new strategies and therapies for the prevention of heart failure in high‐risk patients
topic Publication of this special issue was made possible by AstraZeneca.
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9254668/
https://www.ncbi.nlm.nih.gov/pubmed/35789013
http://dx.doi.org/10.1002/clc.23839
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