In‐hospital course of patients with heart failure with improved ejection fraction in the DELIVER trial

Aims Patients with heart failure (HF) with improved ejection fraction (HFimpEF) may face residual risks of clinical events that are comparable to those experienced by patients with HF whose left ventricular ejection fraction (LVEF) has consistently been above 40%. However, little is known about the...

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Veröffentlicht in:European journal of heart failure 2024-12, Vol.26 (12), p.2532-2540
Hauptverfasser: Pabon, Maria A., Vaduganathan, Muthiah, Claggett, Brian L., Chatur, Safia, Siqueira, Sara, Marti‐Castellote, Pablo, Boer, Rudolf A., Hernandez, Adrian F., Inzucchi, Silvio E., Kosiborod, Mikhail N., Lam, Carolyn S.P., Martinez, Felipe, Shah, Sanjiv J., Desai, Akshay S., Jhund, Pardeep S., McMurray, John J.V., Solomon, Scott D., Vardeny, Orly
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container_end_page 2540
container_issue 12
container_start_page 2532
container_title European journal of heart failure
container_volume 26
creator Pabon, Maria A.
Vaduganathan, Muthiah
Claggett, Brian L.
Chatur, Safia
Siqueira, Sara
Marti‐Castellote, Pablo
Boer, Rudolf A.
Hernandez, Adrian F.
Inzucchi, Silvio E.
Kosiborod, Mikhail N.
Lam, Carolyn S.P.
Martinez, Felipe
Shah, Sanjiv J.
Desai, Akshay S.
Jhund, Pardeep S.
McMurray, John J.V.
Solomon, Scott D.
Vardeny, Orly
description Aims Patients with heart failure (HF) with improved ejection fraction (HFimpEF) may face residual risks of clinical events that are comparable to those experienced by patients with HF whose left ventricular ejection fraction (LVEF) has consistently been above 40%. However, little is known about the clinical course of patients with HFimpEF during hospitalization for HF. Methods and results DELIVER randomized patients with HF and LVEF >40% to dapagliflozin or placebo, including HFimpEF (LVEF previously ≤40%). We evaluated all HF hospitalizations adjudicated by the clinical endpoints committee with available data for determination of in‐hospital course. Complicated hospitalization was defined as any hospitalization requiring intensive care unit stay, intravenous vasopressors/inotropes/vasodilators, invasive or non‐invasive ventilation, mechanical fluid removal, ultrafiltration, or mechanical circulatory support. LVEF changes were extracted using a validated GPT‐3.5, a large language model, via a secure private endpoint. Of the 6263 patients enrolled in DELIVER, 1151 (18%) had HFimpEF. During a median follow‐up of 2.3 years, there were 224 total HF hospitalizations in 144 patients with HFimpEF and 985 in 603 patients with LVEF consistently >40%. Patients with HFimpEF experienced higher rates of complicated HF hospitalization as compared with patients with LVEF consistently >40% (39% vs. 27%; p 40%. In a subset of participants who had at least one LVEF measurement available during HF hospitalization, 66% of those with HFimpEF and 29% of patients with LVEF consistently >40% experienced a reduction in their LVEF to ≤40% from the time of enrolment (p 40%, but had similar in‐hospital mortality. Treatment benefits of dapagliflozin were not modified by hospitalization type. In‐hospital course of patients with heart failure (HF) with improved e
doi_str_mv 10.1002/ejhf.3410
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However, little is known about the clinical course of patients with HFimpEF during hospitalization for HF. Methods and results DELIVER randomized patients with HF and LVEF &gt;40% to dapagliflozin or placebo, including HFimpEF (LVEF previously ≤40%). We evaluated all HF hospitalizations adjudicated by the clinical endpoints committee with available data for determination of in‐hospital course. Complicated hospitalization was defined as any hospitalization requiring intensive care unit stay, intravenous vasopressors/inotropes/vasodilators, invasive or non‐invasive ventilation, mechanical fluid removal, ultrafiltration, or mechanical circulatory support. LVEF changes were extracted using a validated GPT‐3.5, a large language model, via a secure private endpoint. Of the 6263 patients enrolled in DELIVER, 1151 (18%) had HFimpEF. During a median follow‐up of 2.3 years, there were 224 total HF hospitalizations in 144 patients with HFimpEF and 985 in 603 patients with LVEF consistently &gt;40%. Patients with HFimpEF experienced higher rates of complicated HF hospitalization as compared with patients with LVEF consistently &gt;40% (39% vs. 27%; p &lt; 0.001). Among those who experienced a first HF hospitalization, there was no significant difference in length of stay or in‐hospital mortality between patients with HFimpEF versus LVEF consistently &gt;40%. In a subset of participants who had at least one LVEF measurement available during HF hospitalization, 66% of those with HFimpEF and 29% of patients with LVEF consistently &gt;40% experienced a reduction in their LVEF to ≤40% from the time of enrolment (p &lt; 0.001). In the entire DELIVER cohort, dapagliflozin reduced total uncomplicated and complicated HF hospitalizations, irrespective of HFimpEF status (pinteraction ≥0.30). Conclusions Among patients hospitalized for HF in DELIVER, those with HFimpEF experienced a more adverse in‐hospital clinical course, necessitating higher resource utilization beyond standard diuretic therapy compared with patients with HF and LVEF consistently &gt;40%, but had similar in‐hospital mortality. Treatment benefits of dapagliflozin were not modified by hospitalization type. In‐hospital course of patients with heart failure (HF) with improved ejection fraction (HFimpEF) in DELIVER. LVEF, left ventricular ejection fraction.</description><identifier>ISSN: 1388-9842</identifier><identifier>ISSN: 1879-0844</identifier><identifier>EISSN: 1879-0844</identifier><identifier>DOI: 10.1002/ejhf.3410</identifier><identifier>PMID: 39300780</identifier><language>eng</language><publisher>Oxford, UK: John Wiley &amp; Sons, Ltd</publisher><subject>Aged ; Benzhydryl Compounds - therapeutic use ; Female ; Follow-Up Studies ; Glucosides ; Heart failure ; Heart Failure - drug therapy ; Heart Failure - physiopathology ; Heart Failure - therapy ; Heart failure hospitalization ; Heart Failure Phenotypes ; HFimpEF ; Hospital Mortality ; Hospitalization - statistics &amp; numerical data ; Humans ; Male ; Middle Aged ; Sodium-Glucose Transporter 2 Inhibitors - therapeutic use ; Stroke Volume - physiology ; Ventricular Function, Left - physiology</subject><ispartof>European journal of heart failure, 2024-12, Vol.26 (12), p.2532-2540</ispartof><rights>2024 The Author(s). published by John Wiley &amp; Sons Ltd on behalf of European Society of Cardiology.</rights><rights>2024 The Author(s). European Journal of Heart Failure published by John Wiley &amp; Sons Ltd on behalf of European Society of Cardiology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3060-96bfd1f5d2e639a2dbfd0006610a46d7dd13ebaf7d2119c87b05662cc4a113b63</cites><orcidid>0000-0003-1883-0654</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fejhf.3410$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fejhf.3410$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39300780$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pabon, Maria A.</creatorcontrib><creatorcontrib>Vaduganathan, Muthiah</creatorcontrib><creatorcontrib>Claggett, Brian L.</creatorcontrib><creatorcontrib>Chatur, Safia</creatorcontrib><creatorcontrib>Siqueira, Sara</creatorcontrib><creatorcontrib>Marti‐Castellote, Pablo</creatorcontrib><creatorcontrib>Boer, Rudolf A.</creatorcontrib><creatorcontrib>Hernandez, Adrian F.</creatorcontrib><creatorcontrib>Inzucchi, Silvio E.</creatorcontrib><creatorcontrib>Kosiborod, Mikhail N.</creatorcontrib><creatorcontrib>Lam, Carolyn S.P.</creatorcontrib><creatorcontrib>Martinez, Felipe</creatorcontrib><creatorcontrib>Shah, Sanjiv J.</creatorcontrib><creatorcontrib>Desai, Akshay S.</creatorcontrib><creatorcontrib>Jhund, Pardeep S.</creatorcontrib><creatorcontrib>McMurray, John J.V.</creatorcontrib><creatorcontrib>Solomon, Scott D.</creatorcontrib><creatorcontrib>Vardeny, Orly</creatorcontrib><title>In‐hospital course of patients with heart failure with improved ejection fraction in the DELIVER trial</title><title>European journal of heart failure</title><addtitle>Eur J Heart Fail</addtitle><description>Aims Patients with heart failure (HF) with improved ejection fraction (HFimpEF) may face residual risks of clinical events that are comparable to those experienced by patients with HF whose left ventricular ejection fraction (LVEF) has consistently been above 40%. However, little is known about the clinical course of patients with HFimpEF during hospitalization for HF. Methods and results DELIVER randomized patients with HF and LVEF &gt;40% to dapagliflozin or placebo, including HFimpEF (LVEF previously ≤40%). We evaluated all HF hospitalizations adjudicated by the clinical endpoints committee with available data for determination of in‐hospital course. Complicated hospitalization was defined as any hospitalization requiring intensive care unit stay, intravenous vasopressors/inotropes/vasodilators, invasive or non‐invasive ventilation, mechanical fluid removal, ultrafiltration, or mechanical circulatory support. LVEF changes were extracted using a validated GPT‐3.5, a large language model, via a secure private endpoint. Of the 6263 patients enrolled in DELIVER, 1151 (18%) had HFimpEF. During a median follow‐up of 2.3 years, there were 224 total HF hospitalizations in 144 patients with HFimpEF and 985 in 603 patients with LVEF consistently &gt;40%. Patients with HFimpEF experienced higher rates of complicated HF hospitalization as compared with patients with LVEF consistently &gt;40% (39% vs. 27%; p &lt; 0.001). Among those who experienced a first HF hospitalization, there was no significant difference in length of stay or in‐hospital mortality between patients with HFimpEF versus LVEF consistently &gt;40%. In a subset of participants who had at least one LVEF measurement available during HF hospitalization, 66% of those with HFimpEF and 29% of patients with LVEF consistently &gt;40% experienced a reduction in their LVEF to ≤40% from the time of enrolment (p &lt; 0.001). In the entire DELIVER cohort, dapagliflozin reduced total uncomplicated and complicated HF hospitalizations, irrespective of HFimpEF status (pinteraction ≥0.30). Conclusions Among patients hospitalized for HF in DELIVER, those with HFimpEF experienced a more adverse in‐hospital clinical course, necessitating higher resource utilization beyond standard diuretic therapy compared with patients with HF and LVEF consistently &gt;40%, but had similar in‐hospital mortality. Treatment benefits of dapagliflozin were not modified by hospitalization type. In‐hospital course of patients with heart failure (HF) with improved ejection fraction (HFimpEF) in DELIVER. LVEF, left ventricular ejection fraction.</description><subject>Aged</subject><subject>Benzhydryl Compounds - therapeutic use</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Glucosides</subject><subject>Heart failure</subject><subject>Heart Failure - drug therapy</subject><subject>Heart Failure - physiopathology</subject><subject>Heart Failure - therapy</subject><subject>Heart failure hospitalization</subject><subject>Heart Failure Phenotypes</subject><subject>HFimpEF</subject><subject>Hospital Mortality</subject><subject>Hospitalization - statistics &amp; numerical data</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Sodium-Glucose Transporter 2 Inhibitors - therapeutic use</subject><subject>Stroke Volume - physiology</subject><subject>Ventricular Function, Left - physiology</subject><issn>1388-9842</issn><issn>1879-0844</issn><issn>1879-0844</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>EIF</sourceid><recordid>eNp1kcFu1DAQhi0EomXhwAsgH-GQdhxnbeeEUNnSRSshIeBqOfGYeJWNg-206o1H4Bl5ErKkVHDgNDP2p29s_YQ8Z3DGAMpz3HfujFcMHpBTpmRdgKqqh3PPlSpqVZUn5ElKewAmZ_wxOeE1B5AKTkm3HX5-_9GFNPpsetqGKSakwdHRZI9DTvTG5452aGKmzvh-irgc-cMYwzVaintssw8DddEsjR9o7pC-3ey2XzYfaY7e9E_JI2f6hM_u6op8vtx8urgqdh_ebS_e7IqWg4CiFo2zzK1tiYLXprTzCABCMDCVsNJaxrExTtqSsbpVsoG1EGXbVoYx3gi-Iq8X7zg1B7Tt_Idoej1GfzDxVgfj9b83g-_013CtGROKKyFnw8s7QwzfJkxZH3xqse_NgGFKmjOQbK3kjK_IqwVtY0gporvfw0Afo9HHaPQxmpl98ffD7sk_WczA-QLc-B5v_2_Sm_dXl7-VvwBEDZuR</recordid><startdate>202412</startdate><enddate>202412</enddate><creator>Pabon, Maria A.</creator><creator>Vaduganathan, Muthiah</creator><creator>Claggett, Brian L.</creator><creator>Chatur, Safia</creator><creator>Siqueira, Sara</creator><creator>Marti‐Castellote, Pablo</creator><creator>Boer, Rudolf A.</creator><creator>Hernandez, Adrian F.</creator><creator>Inzucchi, Silvio E.</creator><creator>Kosiborod, Mikhail N.</creator><creator>Lam, Carolyn S.P.</creator><creator>Martinez, Felipe</creator><creator>Shah, Sanjiv J.</creator><creator>Desai, Akshay S.</creator><creator>Jhund, Pardeep S.</creator><creator>McMurray, John J.V.</creator><creator>Solomon, Scott D.</creator><creator>Vardeny, Orly</creator><general>John Wiley &amp; Sons, Ltd</general><scope>24P</scope><scope>WIN</scope><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><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-1883-0654</orcidid></search><sort><creationdate>202412</creationdate><title>In‐hospital course of patients with heart failure with improved ejection fraction in the DELIVER trial</title><author>Pabon, Maria A. ; Vaduganathan, Muthiah ; Claggett, Brian L. ; Chatur, Safia ; Siqueira, Sara ; Marti‐Castellote, Pablo ; Boer, Rudolf A. ; Hernandez, Adrian F. ; Inzucchi, Silvio E. ; Kosiborod, Mikhail N. ; Lam, Carolyn S.P. ; Martinez, Felipe ; Shah, Sanjiv J. ; Desai, Akshay S. ; Jhund, Pardeep S. ; McMurray, John J.V. ; Solomon, Scott D. ; Vardeny, Orly</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3060-96bfd1f5d2e639a2dbfd0006610a46d7dd13ebaf7d2119c87b05662cc4a113b63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Aged</topic><topic>Benzhydryl Compounds - therapeutic use</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Glucosides</topic><topic>Heart failure</topic><topic>Heart Failure - drug therapy</topic><topic>Heart Failure - physiopathology</topic><topic>Heart Failure - therapy</topic><topic>Heart failure hospitalization</topic><topic>Heart Failure Phenotypes</topic><topic>HFimpEF</topic><topic>Hospital Mortality</topic><topic>Hospitalization - statistics &amp; numerical data</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Sodium-Glucose Transporter 2 Inhibitors - therapeutic use</topic><topic>Stroke Volume - physiology</topic><topic>Ventricular Function, Left - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pabon, Maria A.</creatorcontrib><creatorcontrib>Vaduganathan, Muthiah</creatorcontrib><creatorcontrib>Claggett, Brian L.</creatorcontrib><creatorcontrib>Chatur, Safia</creatorcontrib><creatorcontrib>Siqueira, Sara</creatorcontrib><creatorcontrib>Marti‐Castellote, Pablo</creatorcontrib><creatorcontrib>Boer, Rudolf A.</creatorcontrib><creatorcontrib>Hernandez, Adrian F.</creatorcontrib><creatorcontrib>Inzucchi, Silvio E.</creatorcontrib><creatorcontrib>Kosiborod, Mikhail N.</creatorcontrib><creatorcontrib>Lam, Carolyn S.P.</creatorcontrib><creatorcontrib>Martinez, Felipe</creatorcontrib><creatorcontrib>Shah, Sanjiv J.</creatorcontrib><creatorcontrib>Desai, Akshay S.</creatorcontrib><creatorcontrib>Jhund, Pardeep S.</creatorcontrib><creatorcontrib>McMurray, John J.V.</creatorcontrib><creatorcontrib>Solomon, Scott D.</creatorcontrib><creatorcontrib>Vardeny, Orly</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Free Content</collection><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><collection>PubMed Central (Full Participant titles)</collection><jtitle>European journal of heart failure</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pabon, Maria A.</au><au>Vaduganathan, Muthiah</au><au>Claggett, Brian L.</au><au>Chatur, Safia</au><au>Siqueira, Sara</au><au>Marti‐Castellote, Pablo</au><au>Boer, Rudolf A.</au><au>Hernandez, Adrian F.</au><au>Inzucchi, Silvio E.</au><au>Kosiborod, Mikhail N.</au><au>Lam, Carolyn S.P.</au><au>Martinez, Felipe</au><au>Shah, Sanjiv J.</au><au>Desai, Akshay S.</au><au>Jhund, Pardeep S.</au><au>McMurray, John J.V.</au><au>Solomon, Scott D.</au><au>Vardeny, Orly</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In‐hospital course of patients with heart failure with improved ejection fraction in the DELIVER trial</atitle><jtitle>European journal of heart failure</jtitle><addtitle>Eur J Heart Fail</addtitle><date>2024-12</date><risdate>2024</risdate><volume>26</volume><issue>12</issue><spage>2532</spage><epage>2540</epage><pages>2532-2540</pages><issn>1388-9842</issn><issn>1879-0844</issn><eissn>1879-0844</eissn><abstract>Aims Patients with heart failure (HF) with improved ejection fraction (HFimpEF) may face residual risks of clinical events that are comparable to those experienced by patients with HF whose left ventricular ejection fraction (LVEF) has consistently been above 40%. However, little is known about the clinical course of patients with HFimpEF during hospitalization for HF. Methods and results DELIVER randomized patients with HF and LVEF &gt;40% to dapagliflozin or placebo, including HFimpEF (LVEF previously ≤40%). We evaluated all HF hospitalizations adjudicated by the clinical endpoints committee with available data for determination of in‐hospital course. Complicated hospitalization was defined as any hospitalization requiring intensive care unit stay, intravenous vasopressors/inotropes/vasodilators, invasive or non‐invasive ventilation, mechanical fluid removal, ultrafiltration, or mechanical circulatory support. LVEF changes were extracted using a validated GPT‐3.5, a large language model, via a secure private endpoint. Of the 6263 patients enrolled in DELIVER, 1151 (18%) had HFimpEF. During a median follow‐up of 2.3 years, there were 224 total HF hospitalizations in 144 patients with HFimpEF and 985 in 603 patients with LVEF consistently &gt;40%. Patients with HFimpEF experienced higher rates of complicated HF hospitalization as compared with patients with LVEF consistently &gt;40% (39% vs. 27%; p &lt; 0.001). Among those who experienced a first HF hospitalization, there was no significant difference in length of stay or in‐hospital mortality between patients with HFimpEF versus LVEF consistently &gt;40%. In a subset of participants who had at least one LVEF measurement available during HF hospitalization, 66% of those with HFimpEF and 29% of patients with LVEF consistently &gt;40% experienced a reduction in their LVEF to ≤40% from the time of enrolment (p &lt; 0.001). In the entire DELIVER cohort, dapagliflozin reduced total uncomplicated and complicated HF hospitalizations, irrespective of HFimpEF status (pinteraction ≥0.30). Conclusions Among patients hospitalized for HF in DELIVER, those with HFimpEF experienced a more adverse in‐hospital clinical course, necessitating higher resource utilization beyond standard diuretic therapy compared with patients with HF and LVEF consistently &gt;40%, but had similar in‐hospital mortality. Treatment benefits of dapagliflozin were not modified by hospitalization type. In‐hospital course of patients with heart failure (HF) with improved ejection fraction (HFimpEF) in DELIVER. LVEF, left ventricular ejection fraction.</abstract><cop>Oxford, UK</cop><pub>John Wiley &amp; Sons, Ltd</pub><pmid>39300780</pmid><doi>10.1002/ejhf.3410</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-1883-0654</orcidid><oa>free_for_read</oa></addata></record>
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subjects Aged
Benzhydryl Compounds - therapeutic use
Female
Follow-Up Studies
Glucosides
Heart failure
Heart Failure - drug therapy
Heart Failure - physiopathology
Heart Failure - therapy
Heart failure hospitalization
Heart Failure Phenotypes
HFimpEF
Hospital Mortality
Hospitalization - statistics & numerical data
Humans
Male
Middle Aged
Sodium-Glucose Transporter 2 Inhibitors - therapeutic use
Stroke Volume - physiology
Ventricular Function, Left - physiology
title In‐hospital course of patients with heart failure with improved ejection fraction in the DELIVER trial
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