Evolving therapies for the management of chronic and acute decompensated heart failure

PURPOSEThe pharmacology, clinical efficacy, and safety profiles of evolving therapies for the management of chronic heart failure (HF) and acute decompensated heart failure (ADHF) are described. SUMMARYHF confers a significant financial burden despite the widespread use of traditional guideline-dire...

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Veröffentlicht in:American journal of health-system pharmacy 2016-11, Vol.73 (21), p.1745-1754
Hauptverfasser: Cook, Jennifer C, Tran, Richard H, Patterson, Herbert J, Rodgers, Jo E
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container_end_page 1754
container_issue 21
container_start_page 1745
container_title American journal of health-system pharmacy
container_volume 73
creator Cook, Jennifer C
Tran, Richard H
Patterson, Herbert J
Rodgers, Jo E
description PURPOSEThe pharmacology, clinical efficacy, and safety profiles of evolving therapies for the management of chronic heart failure (HF) and acute decompensated heart failure (ADHF) are described. SUMMARYHF confers a significant financial burden despite the widespread use of traditional guideline-directed medical therapies such as angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, β-blockers, and aldosterone receptor antagonists, and the rates of HF-related mortality and hospitalization have remained unacceptably high. In response to a demand for novel pharmacologic agents, several therapeutic compounds have recently gained approval or are currently under review by the Food and Drug Administration. Sacubitril–valsartan has demonstrated benefit in reducing cardiovascular mortality and HF-related hospitalizations in clinical trials, while ivabradine and ferric carboxymaltose have proven efficacious in reducing HF-related hospitalizations. Lastly, the role of serelaxin in ADHF is currently under investigation in an ongoing Phase III study. While large, outcome-driven clinical trials are fundamental in informing the clinical application of these therapeutic agents, careful patient selection is imperative to ensuring similar outcomes postmarketing. In addition, optimization of current guideline-directed medical therapy remains essential as new therapies emerge and are incorporated into guideline recommendations. Additional therapeutic agents currently undergoing investigation include bucindolol hydrochloride, cimaglermin alfa, nitroxyl, omecamtiv mecarbil, TRV027, and ularitide. Clinical practitioners should remain abreast of emerging literature so that new therapeutic entities are optimally applied and positive patient outcomes are achieved. CONCLUSIONRecently introduced agents for the treatment of patients with HF include sacubitril–valsartan, ivabradine, and ferric carboxymaltose. Additional agents worthy of attention include serelaxin and other therapies currently under investigation.
doi_str_mv 10.2146/ajhp150635
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SUMMARYHF confers a significant financial burden despite the widespread use of traditional guideline-directed medical therapies such as angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, β-blockers, and aldosterone receptor antagonists, and the rates of HF-related mortality and hospitalization have remained unacceptably high. In response to a demand for novel pharmacologic agents, several therapeutic compounds have recently gained approval or are currently under review by the Food and Drug Administration. Sacubitril–valsartan has demonstrated benefit in reducing cardiovascular mortality and HF-related hospitalizations in clinical trials, while ivabradine and ferric carboxymaltose have proven efficacious in reducing HF-related hospitalizations. Lastly, the role of serelaxin in ADHF is currently under investigation in an ongoing Phase III study. While large, outcome-driven clinical trials are fundamental in informing the clinical application of these therapeutic agents, careful patient selection is imperative to ensuring similar outcomes postmarketing. In addition, optimization of current guideline-directed medical therapy remains essential as new therapies emerge and are incorporated into guideline recommendations. Additional therapeutic agents currently undergoing investigation include bucindolol hydrochloride, cimaglermin alfa, nitroxyl, omecamtiv mecarbil, TRV027, and ularitide. Clinical practitioners should remain abreast of emerging literature so that new therapeutic entities are optimally applied and positive patient outcomes are achieved. CONCLUSIONRecently introduced agents for the treatment of patients with HF include sacubitril–valsartan, ivabradine, and ferric carboxymaltose. Additional agents worthy of attention include serelaxin and other therapies currently under investigation.</description><identifier>ISSN: 1079-2082</identifier><identifier>EISSN: 1535-2900</identifier><identifier>DOI: 10.2146/ajhp150635</identifier><identifier>PMID: 27769970</identifier><language>eng</language><publisher>England: Copyright American Society of Health-System Pharmacists, Inc. All rights reserved</publisher><subject>Acute Disease ; Adrenergic beta-Antagonists - therapeutic use ; Aminobutyrates - therapeutic use ; Angiotensin Receptor Antagonists - therapeutic use ; Angiotensin-Converting Enzyme Inhibitors - therapeutic use ; Benzazepines - therapeutic use ; Cardiovascular Agents - therapeutic use ; Chronic Disease ; Clinical Trials as Topic - methods ; Disease Management ; Drug Combinations ; Ferric Compounds - therapeutic use ; Heart Failure - diagnosis ; Heart Failure - drug therapy ; Heart Failure - physiopathology ; Humans ; Ivabradine ; Maltose - analogs &amp; derivatives ; Maltose - therapeutic use ; Tetrazoles - therapeutic use</subject><ispartof>American journal of health-system pharmacy, 2016-11, Vol.73 (21), p.1745-1754</ispartof><rights>Copyright © 2016 American Society of Health-System Pharmacists, Inc. All rights reserved.</rights><rights>Copyright © 2016 by the American Society of Health-System Pharmacists, Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4023-cec6bc9e62b8352364697fa57252d8ccca39d2724d8932433f40be38f19f59883</citedby><cites>FETCH-LOGICAL-c4023-cec6bc9e62b8352364697fa57252d8ccca39d2724d8932433f40be38f19f59883</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27769970$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cook, Jennifer C</creatorcontrib><creatorcontrib>Tran, Richard H</creatorcontrib><creatorcontrib>Patterson, Herbert J</creatorcontrib><creatorcontrib>Rodgers, Jo E</creatorcontrib><title>Evolving therapies for the management of chronic and acute decompensated heart failure</title><title>American journal of health-system pharmacy</title><addtitle>Am J Health Syst Pharm</addtitle><description>PURPOSEThe pharmacology, clinical efficacy, and safety profiles of evolving therapies for the management of chronic heart failure (HF) and acute decompensated heart failure (ADHF) are described. SUMMARYHF confers a significant financial burden despite the widespread use of traditional guideline-directed medical therapies such as angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, β-blockers, and aldosterone receptor antagonists, and the rates of HF-related mortality and hospitalization have remained unacceptably high. In response to a demand for novel pharmacologic agents, several therapeutic compounds have recently gained approval or are currently under review by the Food and Drug Administration. Sacubitril–valsartan has demonstrated benefit in reducing cardiovascular mortality and HF-related hospitalizations in clinical trials, while ivabradine and ferric carboxymaltose have proven efficacious in reducing HF-related hospitalizations. Lastly, the role of serelaxin in ADHF is currently under investigation in an ongoing Phase III study. While large, outcome-driven clinical trials are fundamental in informing the clinical application of these therapeutic agents, careful patient selection is imperative to ensuring similar outcomes postmarketing. In addition, optimization of current guideline-directed medical therapy remains essential as new therapies emerge and are incorporated into guideline recommendations. Additional therapeutic agents currently undergoing investigation include bucindolol hydrochloride, cimaglermin alfa, nitroxyl, omecamtiv mecarbil, TRV027, and ularitide. Clinical practitioners should remain abreast of emerging literature so that new therapeutic entities are optimally applied and positive patient outcomes are achieved. CONCLUSIONRecently introduced agents for the treatment of patients with HF include sacubitril–valsartan, ivabradine, and ferric carboxymaltose. Additional agents worthy of attention include serelaxin and other therapies currently under investigation.</description><subject>Acute Disease</subject><subject>Adrenergic beta-Antagonists - therapeutic use</subject><subject>Aminobutyrates - therapeutic use</subject><subject>Angiotensin Receptor Antagonists - therapeutic use</subject><subject>Angiotensin-Converting Enzyme Inhibitors - therapeutic use</subject><subject>Benzazepines - therapeutic use</subject><subject>Cardiovascular Agents - therapeutic use</subject><subject>Chronic Disease</subject><subject>Clinical Trials as Topic - methods</subject><subject>Disease Management</subject><subject>Drug Combinations</subject><subject>Ferric Compounds - therapeutic use</subject><subject>Heart Failure - diagnosis</subject><subject>Heart Failure - drug therapy</subject><subject>Heart Failure - physiopathology</subject><subject>Humans</subject><subject>Ivabradine</subject><subject>Maltose - analogs &amp; derivatives</subject><subject>Maltose - therapeutic use</subject><subject>Tetrazoles - therapeutic use</subject><issn>1079-2082</issn><issn>1535-2900</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkMtKxDAUQIMozji68QMkSxGqN0mTNkuR8QEDbtRtyaQ3tmPb1KQd8e-tjI_VfXA4i0PIKYNLzlJ1ZTZVzyQoIffInEkhE64B9qcdMp1wyPmMHMW4AWA8B3VIZjzLlNYZzMnLcuubbd290qHCYPoaI3U-fF-0NZ15xRa7gXpHbRV8V1tqupIaOw5IS7S-7bGLZsCSVmjCQJ2pmzHgMTlwpol48jMX5Pl2-XRzn6we7x5urleJTYGLxKJVa6tR8XUuJBcqVTpzRmZc8jK31hqhS57xtMy14KkQLoU1itwx7aTOc7Eg5ztvH_z7iHEo2jpabBrToR9jwSatZEJJMaEXO9QGH2NAV_Shbk34LBgU3x2L_44TfPbjHdctln_ob7gJSHfAh28GDPGtGT8wFFOEZqgKAEiF4tkUnynGgEEyvZgQX3u9fXI</recordid><startdate>20161101</startdate><enddate>20161101</enddate><creator>Cook, Jennifer C</creator><creator>Tran, Richard H</creator><creator>Patterson, Herbert J</creator><creator>Rodgers, Jo E</creator><general>Copyright American Society of Health-System Pharmacists, Inc. All rights reserved</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20161101</creationdate><title>Evolving therapies for the management of chronic and acute decompensated heart failure</title><author>Cook, Jennifer C ; Tran, Richard H ; Patterson, Herbert J ; Rodgers, Jo E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4023-cec6bc9e62b8352364697fa57252d8ccca39d2724d8932433f40be38f19f59883</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Acute Disease</topic><topic>Adrenergic beta-Antagonists - therapeutic use</topic><topic>Aminobutyrates - therapeutic use</topic><topic>Angiotensin Receptor Antagonists - therapeutic use</topic><topic>Angiotensin-Converting Enzyme Inhibitors - therapeutic use</topic><topic>Benzazepines - therapeutic use</topic><topic>Cardiovascular Agents - therapeutic use</topic><topic>Chronic Disease</topic><topic>Clinical Trials as Topic - methods</topic><topic>Disease Management</topic><topic>Drug Combinations</topic><topic>Ferric Compounds - therapeutic use</topic><topic>Heart Failure - diagnosis</topic><topic>Heart Failure - drug therapy</topic><topic>Heart Failure - physiopathology</topic><topic>Humans</topic><topic>Ivabradine</topic><topic>Maltose - analogs &amp; derivatives</topic><topic>Maltose - therapeutic use</topic><topic>Tetrazoles - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cook, Jennifer C</creatorcontrib><creatorcontrib>Tran, Richard H</creatorcontrib><creatorcontrib>Patterson, Herbert J</creatorcontrib><creatorcontrib>Rodgers, Jo E</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of health-system pharmacy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cook, Jennifer C</au><au>Tran, Richard H</au><au>Patterson, Herbert J</au><au>Rodgers, Jo E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evolving therapies for the management of chronic and acute decompensated heart failure</atitle><jtitle>American journal of health-system pharmacy</jtitle><addtitle>Am J Health Syst Pharm</addtitle><date>2016-11-01</date><risdate>2016</risdate><volume>73</volume><issue>21</issue><spage>1745</spage><epage>1754</epage><pages>1745-1754</pages><issn>1079-2082</issn><eissn>1535-2900</eissn><abstract>PURPOSEThe pharmacology, clinical efficacy, and safety profiles of evolving therapies for the management of chronic heart failure (HF) and acute decompensated heart failure (ADHF) are described. SUMMARYHF confers a significant financial burden despite the widespread use of traditional guideline-directed medical therapies such as angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, β-blockers, and aldosterone receptor antagonists, and the rates of HF-related mortality and hospitalization have remained unacceptably high. In response to a demand for novel pharmacologic agents, several therapeutic compounds have recently gained approval or are currently under review by the Food and Drug Administration. Sacubitril–valsartan has demonstrated benefit in reducing cardiovascular mortality and HF-related hospitalizations in clinical trials, while ivabradine and ferric carboxymaltose have proven efficacious in reducing HF-related hospitalizations. Lastly, the role of serelaxin in ADHF is currently under investigation in an ongoing Phase III study. While large, outcome-driven clinical trials are fundamental in informing the clinical application of these therapeutic agents, careful patient selection is imperative to ensuring similar outcomes postmarketing. In addition, optimization of current guideline-directed medical therapy remains essential as new therapies emerge and are incorporated into guideline recommendations. Additional therapeutic agents currently undergoing investigation include bucindolol hydrochloride, cimaglermin alfa, nitroxyl, omecamtiv mecarbil, TRV027, and ularitide. Clinical practitioners should remain abreast of emerging literature so that new therapeutic entities are optimally applied and positive patient outcomes are achieved. CONCLUSIONRecently introduced agents for the treatment of patients with HF include sacubitril–valsartan, ivabradine, and ferric carboxymaltose. Additional agents worthy of attention include serelaxin and other therapies currently under investigation.</abstract><cop>England</cop><pub>Copyright American Society of Health-System Pharmacists, Inc. All rights reserved</pub><pmid>27769970</pmid><doi>10.2146/ajhp150635</doi><tpages>10</tpages></addata></record>
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source Journals@Ovid Ovid Autoload; Oxford University Press Journals All Titles (1996-Current); MEDLINE
subjects Acute Disease
Adrenergic beta-Antagonists - therapeutic use
Aminobutyrates - therapeutic use
Angiotensin Receptor Antagonists - therapeutic use
Angiotensin-Converting Enzyme Inhibitors - therapeutic use
Benzazepines - therapeutic use
Cardiovascular Agents - therapeutic use
Chronic Disease
Clinical Trials as Topic - methods
Disease Management
Drug Combinations
Ferric Compounds - therapeutic use
Heart Failure - diagnosis
Heart Failure - drug therapy
Heart Failure - physiopathology
Humans
Ivabradine
Maltose - analogs & derivatives
Maltose - therapeutic use
Tetrazoles - therapeutic use
title Evolving therapies for the management of chronic and acute decompensated heart failure
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