<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>5(3)</volume><submitter>Mignone JL</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Limited real-world evidence exists for outcomes with contemporary guideline-directed medical therapy (GDMT) or GDMT with implantable cardioverter-defibrillator (ICD)/cardiac resynchronization therapy defibrillator (CRT-D) therapy for patients with heart failure with reduced ejection fraction (HFrEF) and left ventricular ejection fraction (LVEF) ≤35%.&lt;h4>Objective&lt;/h4>The present study aimed to assess survival associated with GDMT or GDMT with ICD/CRT-D therapy.&lt;h4>Methods&lt;/h4>This retrospective observational study included real-world de-identified data from January 1, 2016, to December 19, 2023, from 24 U.S. institutions per participating institutional agreements (egnite Database; egnite, Inc.). Patients with a diagnosis of HFrEF and an echocardiographic study documenting LVEF ≤35% were included for analysis.&lt;h4>Results&lt;/h4>Of 43,591 patients with eligible index event of LVEF ≤35%, prescription history through ≥1 year preindex, and no ICD/CRT-D therapy preindex, mean ± standard deviation age at index was 71.2 ± 13.2 years; 14,805 (34.0%) patients were female. At 24 months, an estimated 99.1% (95% confidence interval [CI] 99.0%-99.2%), 89.9% (95% CI 89.7%-90.1%), 54.8% (95% CI 54.4%-55.2%), and 17.2% (95% CI 16.9%-17.5%), had ≥1, 2, 3, or all 4 GDMT classes prescribed, respectively; an estimated 15.7% (95% CI 15.3%-16.1%) had device placement. Of those without a device, by 24 months, an estimated 45.1% (95% CI 44.4%-45.7%) had a documented LVEF >35%. Counts of GDMT classes prescribed as well as ICD/CRT-D device therapy were associated with lower mortality risk in this population, even after adjustment for patient age, sex, and comorbidities.&lt;h4>Conclusion&lt;/h4>Both GDMT classes prescribed and device therapy were independently associated with lower mortality risk, even in the presence of more GDMT options for this more contemporary population.</pubmed_abstract><journal>Heart rhythm O2</journal><pagination>168-173</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10980920</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Outcomes with guideline-directed medical therapy and cardiac implantable electronic device therapies for patients with heart failure with reduced ejection fraction.</pubmed_title><pmcid>PMC10980920</pmcid><pubmed_authors>Dobbles M</pubmed_authors><pubmed_authors>Fonarow GC</pubmed_authors><pubmed_authors>Alexander KM</pubmed_authors><pubmed_authors>Mignone JL</pubmed_authors><pubmed_authors>Ellenbogen KA</pubmed_authors><pubmed_authors>Eberst K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Outcomes with guideline-directed medical therapy and cardiac implantable electronic device therapies for patients with heart failure with reduced ejection fraction.</name><description>&lt;h4>Background&lt;/h4>Limited real-world evidence exists for outcomes with contemporary guideline-directed medical therapy (GDMT) or GDMT with implantable cardioverter-defibrillator (ICD)/cardiac resynchronization therapy defibrillator (CRT-D) therapy for patients with heart failure with reduced ejection fraction (HFrEF) and left ventricular ejection fraction (LVEF) ≤35%.&lt;h4>Objective&lt;/h4>The present study aimed to assess survival associated with GDMT or GDMT with ICD/CRT-D therapy.&lt;h4>Methods&lt;/h4>This retrospective observational study included real-world de-identified data from January 1, 2016, to December 19, 2023, from 24 U.S. institutions per participating institutional agreements (egnite Database; egnite, Inc.). Patients with a diagnosis of HFrEF and an echocardiographic study documenting LVEF ≤35% were included for analysis.&lt;h4>Results&lt;/h4>Of 43,591 patients with eligible index event of LVEF ≤35%, prescription history through ≥1 year preindex, and no ICD/CRT-D therapy preindex, mean ± standard deviation age at index was 71.2 ± 13.2 years; 14,805 (34.0%) patients were female. At 24 months, an estimated 99.1% (95% confidence interval [CI] 99.0%-99.2%), 89.9% (95% CI 89.7%-90.1%), 54.8% (95% CI 54.4%-55.2%), and 17.2% (95% CI 16.9%-17.5%), had ≥1, 2, 3, or all 4 GDMT classes prescribed, respectively; an estimated 15.7% (95% CI 15.3%-16.1%) had device placement. Of those without a device, by 24 months, an estimated 45.1% (95% CI 44.4%-45.7%) had a documented LVEF >35%. Counts of GDMT classes prescribed as well as ICD/CRT-D device therapy were associated with lower mortality risk in this population, even after adjustment for patient age, sex, and comorbidities.&lt;h4>Conclusion&lt;/h4>Both GDMT classes prescribed and device therapy were independently associated with lower mortality risk, even in the presence of more GDMT options for this more contemporary population.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2025-04-19T10:13:46.027Z</modification><creation>2025-04-19T10:13:46.027Z</creation></dates><accession>S-EPMC10980920</accession><cross_references><pubmed>38560378</pubmed><doi>10.1016/j.hroo.2024.01.004</doi></cross_references></HashMap>