New strategies and therapies for the prevention of heart failure in high-risk patients.
New strategies and therapies for the prevention of heart failure in high-risk patients.
复制标题
DOI:
10.1002/clc.23839
复制
发表时间:
2022-06
影响因子:
2.7
通讯作者:
中科院分区:
文献类型:
--
作者:
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.
登录
查看更多内容
影响因子:
20.1
作者:
Ambale-Venkatesh B;Yang X;Wu CO;Liu K;Hundley WG;McClelland R;Gomes AS;Folsom AR;Shea S;Guallar E;Bluemke DA;Lima JAC
通讯作者:
Lima JAC
影响因子:
7.4
作者:
Cresci, Sharon;Pereira, Naveen L.;Wolf, Matthew J.
通讯作者:
Wolf, Matthew J.
影响因子:
158.5
作者:
Cleland, JGF;Daubert, J;Khan, NK
通讯作者:
Khan, NK
影响因子:
37.8
作者:
Shah AM;Claggett B;Loehr LR;Chang PP;Matsushita K;Kitzman D;Konety S;Kucharska-Newton A;Sueta CA;Mosley TH;Wright JD;Coresh J;Heiss G;Folsom AR;Solomon SD
通讯作者:
Solomon SD
影响因子:
13
作者:
Aimo, Alberto;Vergaro, Giuseppe;Emdin, Michele
通讯作者:
Emdin, Michele