Heart Failure With Improved Ejection Fraction: Clinical Characteristics, Correlates of Recovery, and Survival Results From the Valsartan Heart Failure Trial
Heart failure with recovered or improved ejection fraction (HFiEF) has been proposed as a new category of HF. Whether HFiEF is clinically distinct from HF with persistently reduced ejection fraction remains to be validated. Of the 5010 subjects enrolled in the Valsartan Heart Failure Trial (Val-HeFT...
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Published in | Circulation. Heart failure Vol. 9; no. 7 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
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United States
01.07.2016
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ISSN | 1941-3289 1941-3297 1941-3297 |
DOI | 10.1161/CIRCHEARTFAILURE.116.003123 |
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Abstract | Heart failure with recovered or improved ejection fraction (HFiEF) has been proposed as a new category of HF. Whether HFiEF is clinically distinct from HF with persistently reduced ejection fraction remains to be validated.
Of the 5010 subjects enrolled in the Valsartan Heart Failure Trial (Val-HeFT), 3519 had a baseline left ventricular EF of <35% and a follow-up echocardiographic assessment of EF at 12 months. Of these, 321 (9.1%) patients who had a 12-month EF of >40% constituted the subgroup with HFiEF. EF improved from 28.7±5.6% to 46.5±5.6% in the subgroup with HFiEF and remained reduced (25.2±6.2% and 27.5±7.1%) in the subgroup with HF with reduced ejection fraction. The group with HFiEF had a less severe hemodynamic, biomarker, and neurohormonal profile, and it was treated with a more intense HF medication regimen. Subjects who had higher blood pressure and those treated with a β-blocker or randomized to valsartan had greater odds of being in the HFiEF group, whereas those with an ischemic pathogenesis, a more dilated left ventricle, and a detectable hs-troponin had lower odds of an improvement in EF. Recovery of the EF to >40% was associated with a better survival compared with persistently reduced EF.
Our data support HFiEF as a stratum of HF with reduced ejection fraction with a more favorable outcome, which occurs in a minority of patients with HF with reduced ejection fraction who have a lower prevalence of ischemic heart disease, a less severe hemodynamic, biomarker, and neurohormonal profile, and who are treated with a more intense HF medication regimen.
URL: http://www.clinicaltrials.gov. Unique identifier: NCT00336336. |
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AbstractList | Heart failure with recovered or improved ejection fraction (HFiEF) has been proposed as a new category of HF. Whether HFiEF is clinically distinct from HF with persistently reduced ejection fraction remains to be validated.
Of the 5010 subjects enrolled in the Valsartan Heart Failure Trial (Val-HeFT), 3519 had a baseline left ventricular EF of <35% and a follow-up echocardiographic assessment of EF at 12 months. Of these, 321 (9.1%) patients who had a 12-month EF of >40% constituted the subgroup with HFiEF. EF improved from 28.7±5.6% to 46.5±5.6% in the subgroup with HFiEF and remained reduced (25.2±6.2% and 27.5±7.1%) in the subgroup with HF with reduced ejection fraction. The group with HFiEF had a less severe hemodynamic, biomarker, and neurohormonal profile, and it was treated with a more intense HF medication regimen. Subjects who had higher blood pressure and those treated with a β-blocker or randomized to valsartan had greater odds of being in the HFiEF group, whereas those with an ischemic pathogenesis, a more dilated left ventricle, and a detectable hs-troponin had lower odds of an improvement in EF. Recovery of the EF to >40% was associated with a better survival compared with persistently reduced EF.
Our data support HFiEF as a stratum of HF with reduced ejection fraction with a more favorable outcome, which occurs in a minority of patients with HF with reduced ejection fraction who have a lower prevalence of ischemic heart disease, a less severe hemodynamic, biomarker, and neurohormonal profile, and who are treated with a more intense HF medication regimen.
URL: http://www.clinicaltrials.gov. Unique identifier: NCT00336336. Heart failure with recovered or improved ejection fraction (HFiEF) has been proposed as a new category of HF. Whether HFiEF is clinically distinct from HF with persistently reduced ejection fraction remains to be validated.BACKGROUNDHeart failure with recovered or improved ejection fraction (HFiEF) has been proposed as a new category of HF. Whether HFiEF is clinically distinct from HF with persistently reduced ejection fraction remains to be validated.Of the 5010 subjects enrolled in the Valsartan Heart Failure Trial (Val-HeFT), 3519 had a baseline left ventricular EF of <35% and a follow-up echocardiographic assessment of EF at 12 months. Of these, 321 (9.1%) patients who had a 12-month EF of >40% constituted the subgroup with HFiEF. EF improved from 28.7±5.6% to 46.5±5.6% in the subgroup with HFiEF and remained reduced (25.2±6.2% and 27.5±7.1%) in the subgroup with HF with reduced ejection fraction. The group with HFiEF had a less severe hemodynamic, biomarker, and neurohormonal profile, and it was treated with a more intense HF medication regimen. Subjects who had higher blood pressure and those treated with a β-blocker or randomized to valsartan had greater odds of being in the HFiEF group, whereas those with an ischemic pathogenesis, a more dilated left ventricle, and a detectable hs-troponin had lower odds of an improvement in EF. Recovery of the EF to >40% was associated with a better survival compared with persistently reduced EF.METHODS AND RESULTSOf the 5010 subjects enrolled in the Valsartan Heart Failure Trial (Val-HeFT), 3519 had a baseline left ventricular EF of <35% and a follow-up echocardiographic assessment of EF at 12 months. Of these, 321 (9.1%) patients who had a 12-month EF of >40% constituted the subgroup with HFiEF. EF improved from 28.7±5.6% to 46.5±5.6% in the subgroup with HFiEF and remained reduced (25.2±6.2% and 27.5±7.1%) in the subgroup with HF with reduced ejection fraction. The group with HFiEF had a less severe hemodynamic, biomarker, and neurohormonal profile, and it was treated with a more intense HF medication regimen. Subjects who had higher blood pressure and those treated with a β-blocker or randomized to valsartan had greater odds of being in the HFiEF group, whereas those with an ischemic pathogenesis, a more dilated left ventricle, and a detectable hs-troponin had lower odds of an improvement in EF. Recovery of the EF to >40% was associated with a better survival compared with persistently reduced EF.Our data support HFiEF as a stratum of HF with reduced ejection fraction with a more favorable outcome, which occurs in a minority of patients with HF with reduced ejection fraction who have a lower prevalence of ischemic heart disease, a less severe hemodynamic, biomarker, and neurohormonal profile, and who are treated with a more intense HF medication regimen.CONCLUSIONSOur data support HFiEF as a stratum of HF with reduced ejection fraction with a more favorable outcome, which occurs in a minority of patients with HF with reduced ejection fraction who have a lower prevalence of ischemic heart disease, a less severe hemodynamic, biomarker, and neurohormonal profile, and who are treated with a more intense HF medication regimen.URL: http://www.clinicaltrials.gov. Unique identifier: NCT00336336.CLINICAL TRIAL REGISTRATIONURL: http://www.clinicaltrials.gov. Unique identifier: NCT00336336. |
Author | Cohn, Jay N. Rector, Thomas S. Anand, Inder S. Florea, Viorel G. |
Author_xml | – sequence: 1 givenname: Viorel G. surname: Florea fullname: Florea, Viorel G. organization: From the Division of Cardiology (V.G.F., I.S.A.) and Center for Chronic Disease Outcomes Research (T.S.R), Minneapolis Veterans Affairs Health Care System, MN; and Department of Medicine, University of Minnesota, Minneapolis (V.G.F., T.S.R., J.N.C.) – sequence: 2 givenname: Thomas S. surname: Rector fullname: Rector, Thomas S. organization: From the Division of Cardiology (V.G.F., I.S.A.) and Center for Chronic Disease Outcomes Research (T.S.R), Minneapolis Veterans Affairs Health Care System, MN; and Department of Medicine, University of Minnesota, Minneapolis (V.G.F., T.S.R., J.N.C.) – sequence: 3 givenname: Inder S. surname: Anand fullname: Anand, Inder S. organization: From the Division of Cardiology (V.G.F., I.S.A.) and Center for Chronic Disease Outcomes Research (T.S.R), Minneapolis Veterans Affairs Health Care System, MN; and Department of Medicine, University of Minnesota, Minneapolis (V.G.F., T.S.R., J.N.C.) – sequence: 4 givenname: Jay N. surname: Cohn fullname: Cohn, Jay N. organization: From the Division of Cardiology (V.G.F., I.S.A.) and Center for Chronic Disease Outcomes Research (T.S.R), Minneapolis Veterans Affairs Health Care System, MN; and Department of Medicine, University of Minnesota, Minneapolis (V.G.F., T.S.R., J.N.C.) |
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SubjectTerms | Adrenergic beta-Antagonists - therapeutic use Aged Angiotensin II Type 1 Receptor Blockers - adverse effects Angiotensin II Type 1 Receptor Blockers - therapeutic use Angiotensin-Converting Enzyme Inhibitors - therapeutic use Biomarkers - blood Double-Blind Method Drug Therapy, Combination Echocardiography Female Heart Failure - diagnostic imaging Heart Failure - drug therapy Heart Failure - mortality Heart Failure - physiopathology Humans Kaplan-Meier Estimate Male Middle Aged Mineralocorticoid Receptor Antagonists - therapeutic use Recovery of Function Stroke Volume - drug effects Time Factors Treatment Outcome Valsartan - adverse effects Valsartan - therapeutic use Ventricular Function, Left - drug effects |
Subtitle | Results From the Valsartan Heart Failure Trial |
Title | Heart Failure With Improved Ejection Fraction: Clinical Characteristics, Correlates of Recovery, and Survival |
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