The relationship between left ventricular ejection fraction and mortality in patients with acute heart failure: insights from the ASCEND-HF Trial

被引:56
|
作者
Toma, Mustafa [1 ]
Ezekowitz, Justin A. [2 ]
Bakal, Jeffrey A. [3 ]
O'Connor, Christopher M. [4 ]
Hernandez, Adrian F. [4 ]
Sardar, Muhammad Rizwan [5 ]
Zolty, Ronald [5 ]
Massie, Barry M. [6 ]
Swedberg, Karl [7 ]
Armstrong, Paul W. [3 ]
Starling, Randall C. [8 ]
机构
[1] Univ British Columbia, St Pauls Hosp, Div Cardiol, Vancouver, BC V5Z 1M9, Canada
[2] Univ Alberta, Mazankowski Alberta Heart Inst, Div Cardiol, Dept Med, Edmonton, AB T6G 2B7, Canada
[3] Univ Alberta, Canadian VIGOUR Ctr, Edmonton, AB T6G 2B7, Canada
[4] Duke Clin Res Inst, Durham, NC USA
[5] Montefiore Med Ctr, Div Cardiol, Bronx, NY 10467 USA
[6] San Francisco VA Med Ctr, Div Cardiol, San Francisco, CA USA
[7] Ostra Goteborg Univ, Sahlgrenska Univ Hosp, Gothenburg, Sweden
[8] Cleveland Clin, Inst Heart & Vasc, Kaufman Ctr Heart Failure, Dept Cardiovasc Med, Cleveland, OH 44106 USA
关键词
Acute heart failure; Ejection fraction; Clinical trial; Outcomes; PRESERVED SYSTOLIC FUNCTION; BRAIN NATRIURETIC PEPTIDE; NATIONAL REGISTRY ADHERE; LONG-TERM OUTCOMES; EMERGENCY-DEPARTMENT; ATRIAL-FIBRILLATION; DYSFUNCTION; DIAGNOSIS; CANDESARTAN; MANAGEMENT;
D O I
10.1002/ejhf.19
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim Acute decompensated heart failure (ADHF) is associated with significant morbidity and mortality but the relationship between LVEF and outcomes is unclear. We explored the association between LVEF and 30 and 180day mortality in 7007 ADHF patients enrolled in the Acute Studies of Nesiritide in Decompensated Heart Failure (ASCEND-HF) trial. Methods and results We explored the association between LVEF and 30 and 180 day mortality in 7007 ADHF patients enrolled in the Acute Studies of Nesiritide in Decompensated Heart Failure (ASCEND-HF) trial. LVEF was analysed both as a continuous variable and according to three categories: < 40% (LowEF), 40-50% [intermediate EF (IntEF)], and > 50% [preserved ejection fraction (PresEF)]. Of the patients in the trial, 4474 (78.7%) had LowEF, 674 (11.9%) had IntEF, and 539 (9.5%) had PresEF. The unadjusted 30 and 180 day mortality was similar for LowEF (3.7%, 12.3%), IntEF (3.4%, 13.1%), and PresEF (4.3%, 14.1%), respectively (P > 0.05). After multivariable adjustment, the hazard ratio (HR) for 180 day mortality remained similar for the LowEF [HR 0.96, 95% confidence interval (CI) 0.75-1.24; P = 0.77] and IntEF (0.91, 95% CI 0.66-1.3; P = 0.58) compared to PresEF patients. By contrast, when LVEF was evaluated as a continuous measure, it exhibited a U-shaped pattern with mortality. After matching for age and sex, the mortality risk attributed to LVEF was attenuated, as the LVEF increased as a continuous variable over 35%. However, in patients with EF < 35%, the mortality risk continue to increase as the LVEF declined. Conclusions Among patients with ADHF, the unadjusted mortality rates are similar across LVEF strata. However, after accounting for key patient variables, the mortality risk increases as EF falls below 35%. These data will be useful in planning future studies of ADHF. Clinical Trial Registration identifier: NCT00475852
引用
收藏
页码:334 / 341
页数:8
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