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Optimizing Foundational Therapies in Patients With HFrEF: How Do We Translate These Findings Into Clinical Care?
Given the high risk of adverse outcomes in patients with heart failure and reduced ejection fraction (HFrEF), there is an urgent need for the initiation and titration of guideline-directed medical therapy (GDMT) that can reduce the risk of morbidity and mortality. Clinical practice guidelines are no...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9156437/ https://www.ncbi.nlm.nih.gov/pubmed/35663626 http://dx.doi.org/10.1016/j.jacbts.2021.10.018 |
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author | Sharma, Abhinav Verma, Subodh Bhatt, Deepak L. Connelly, Kim A. Swiggum, Elizabeth Vaduganathan, Muthiah Zieroth, Shelley Butler, Javed |
author_facet | Sharma, Abhinav Verma, Subodh Bhatt, Deepak L. Connelly, Kim A. Swiggum, Elizabeth Vaduganathan, Muthiah Zieroth, Shelley Butler, Javed |
author_sort | Sharma, Abhinav |
collection | PubMed |
description | Given the high risk of adverse outcomes in patients with heart failure and reduced ejection fraction (HFrEF), there is an urgent need for the initiation and titration of guideline-directed medical therapy (GDMT) that can reduce the risk of morbidity and mortality. Clinical practice guidelines are now emphasizing the need for early and rapid initiation of therapies that have cardiovascular benefit. Recognizing that there are many barriers to GDMT initiation and optimization, health care providers should aim to introduce the 4 pillars of quadruple therapy now recommended by most clinical practice guidelines: angiotensin receptor–neprilysin inhibitors, beta-blockers, mineralocorticoid receptor antagonists, and sodium–glucose co-transporter 2 inhibitors. A large proportion of patients with HFrEF do not have clinical contraindications to GDMT but are not treated with these therapies. Early initiation of low-dose combination therapy should be tolerated by most patients. However, patient-related factors such as hemodynamics, frailty, and laboratory values will need consideration for maximum tolerated GDMT. GDMT initiation in acute heart failure hospitalization represents another important avenue to improve use of GDMT. Finally, removal of therapies that do not have clear cardiovascular benefit should be considered to lower polypharmacy and reduce the risk of adverse side effects. Future prospective studies aimed at guiding optimal implementation of quadruple therapy are warranted to reduce morbidity and mortality in patients with HFrEF. |
format | Online Article Text |
id | pubmed-9156437 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-91564372022-06-02 Optimizing Foundational Therapies in Patients With HFrEF: How Do We Translate These Findings Into Clinical Care? Sharma, Abhinav Verma, Subodh Bhatt, Deepak L. Connelly, Kim A. Swiggum, Elizabeth Vaduganathan, Muthiah Zieroth, Shelley Butler, Javed JACC Basic Transl Sci State-of-the-Art Review Given the high risk of adverse outcomes in patients with heart failure and reduced ejection fraction (HFrEF), there is an urgent need for the initiation and titration of guideline-directed medical therapy (GDMT) that can reduce the risk of morbidity and mortality. Clinical practice guidelines are now emphasizing the need for early and rapid initiation of therapies that have cardiovascular benefit. Recognizing that there are many barriers to GDMT initiation and optimization, health care providers should aim to introduce the 4 pillars of quadruple therapy now recommended by most clinical practice guidelines: angiotensin receptor–neprilysin inhibitors, beta-blockers, mineralocorticoid receptor antagonists, and sodium–glucose co-transporter 2 inhibitors. A large proportion of patients with HFrEF do not have clinical contraindications to GDMT but are not treated with these therapies. Early initiation of low-dose combination therapy should be tolerated by most patients. However, patient-related factors such as hemodynamics, frailty, and laboratory values will need consideration for maximum tolerated GDMT. GDMT initiation in acute heart failure hospitalization represents another important avenue to improve use of GDMT. Finally, removal of therapies that do not have clear cardiovascular benefit should be considered to lower polypharmacy and reduce the risk of adverse side effects. Future prospective studies aimed at guiding optimal implementation of quadruple therapy are warranted to reduce morbidity and mortality in patients with HFrEF. Elsevier 2022-03-02 /pmc/articles/PMC9156437/ /pubmed/35663626 http://dx.doi.org/10.1016/j.jacbts.2021.10.018 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | State-of-the-Art Review Sharma, Abhinav Verma, Subodh Bhatt, Deepak L. Connelly, Kim A. Swiggum, Elizabeth Vaduganathan, Muthiah Zieroth, Shelley Butler, Javed Optimizing Foundational Therapies in Patients With HFrEF: How Do We Translate These Findings Into Clinical Care? |
title | Optimizing Foundational Therapies in Patients With HFrEF: How Do We Translate These Findings Into Clinical Care? |
title_full | Optimizing Foundational Therapies in Patients With HFrEF: How Do We Translate These Findings Into Clinical Care? |
title_fullStr | Optimizing Foundational Therapies in Patients With HFrEF: How Do We Translate These Findings Into Clinical Care? |
title_full_unstemmed | Optimizing Foundational Therapies in Patients With HFrEF: How Do We Translate These Findings Into Clinical Care? |
title_short | Optimizing Foundational Therapies in Patients With HFrEF: How Do We Translate These Findings Into Clinical Care? |
title_sort | optimizing foundational therapies in patients with hfref: how do we translate these findings into clinical care? |
topic | State-of-the-Art Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9156437/ https://www.ncbi.nlm.nih.gov/pubmed/35663626 http://dx.doi.org/10.1016/j.jacbts.2021.10.018 |
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