Ferric Carboxymaltose in Heart Failure with Iron Deficiency

被引:72
|
作者
Mentz, Robert J. [1 ,3 ]
Garg, Jyotsna [3 ]
Rockhold, Frank W. [2 ,3 ]
Butler, Javed [4 ,5 ]
De Pasquale, Carmine G. [6 ]
Ezekowitz, Justin A. [9 ]
Lewis, Gregory D. [12 ,13 ]
O'Meara, Eileen [10 ,11 ]
Ponikowski, Piotr [14 ]
Troughton, Richard W. [15 ]
Wong, Yee Weng [7 ,8 ,16 ]
She, Lilin [3 ]
Harrington, Josephine [1 ,3 ]
Adamczyk, Robert [17 ]
Blackman, Nicole [17 ]
Hernandez, Adrian F. [1 ,3 ]
机构
[1] Duke Univ, Sch Med, Dept Med, Div Cardiol, 40 Duke Med Cir, Durham, NC 27710 USA
[2] Duke Univ, Sch Med, Dept Biostat & Bioinformat, Durham, NC 27710 USA
[3] Duke Clin Res Inst, Durham, NC USA
[4] Baylor Scott & White Res Inst, Dallas, TX USA
[5] Univ Mississippi, Dept Med, Jackson, MS USA
[6] Flinders Univ S Australia, Flinders Med Ctr, Adelaide, SA, Australia
[7] Univ Queensland, Prince Charles Hosp, Dept Cardiol, Brisbane, Qld, Australia
[8] Univ Queensland, Fac Med, Brisbane, Qld, Australia
[9] Univ Alberta, Canadian VIGOUR Ctr, Edmonton, AB, Canada
[10] Montreal Heart Inst, Montreal, PQ, Canada
[11] Univ Montreal, Montreal, PQ, Canada
[12] Massachusetts Gen Hosp, Cardiol Div, Boston, MA 02114 USA
[13] Massachusetts Gen Hosp, Cardiovasc Res Ctr, Boston, MA 02114 USA
[14] Wroclaw Med Univ, Univ Hosp, Ctr Heart Dis, Wroclaw, Poland
[15] Univ Otago, Christchurch Heart Inst, Christchurch, New Zealand
[16] Mayo Clin, Dept Cardiovasc Med, Rochester, MN USA
[17] Amer Regent, Shirley, NY USA
来源
NEW ENGLAND JOURNAL OF MEDICINE | 2023年 / 389卷 / 11期
关键词
EXERCISE CAPACITY;
D O I
10.1056/NEJMoa2304968
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Ferric carboxymaltose therapy reduces symptoms and improves quality of life in patients who have heart failure with a reduced ejection fraction and iron deficiency. Additional evidence about the effects of ferric carboxymaltose on clinical events is needed. METHODS In this double-blind, randomized trial, we assigned ambulatory patients with heart failure, a left ventricular ejection fraction of 40% or less, and iron deficiency, in a 1:1 ratio, to receive intravenous ferric carboxymaltose or placebo, in addition to standard therapy for heart failure. Ferric carboxymaltose or placebo was given every 6 months as needed on the basis of iron indexes and hemoglobin levels. The primary outcome was a hierarchical composite of death within 12 months after randomization, hospitalizations for heart failure within 12 months after randomization, or change from baseline to 6 months in the 6-minute walk distance. The significance level was set at 0.01. RESULTS We enrolled 3065 patients, of whom 1532 were randomly assigned to the ferric carboxymaltose group and 1533 to the placebo group. Death by month 12 occurred in 131 patients (8.6%) in the ferric carboxymaltose group and 158 (10.3%) in the placebo group; a total of 297 and 332 hospitalizations for heart failure, respectively, occurred by month 12; and the mean (SD) change from baseline to 6 months in the 6-minute walk distance was 8 +/- 60 and 4 +/- 59 m, respectively (Wilcoxon-Mann-Whitney P=0.02; unmatched win ratio, 1.10; 99% confidence interval, 0.99 to 1.23). Repeated dosing of ferric carboxymaltose appeared to be safe with an acceptable adverse-event profile in the majority of patients. The number of patients with serious adverse events occurring during the treatment period was similar in the two groups (413 patients [27.0%] in the ferric carboxymaltose group and 401 [26.2%] in the placebo group). CONCLUSIONS Among ambulatory patients who had heart failure with a reduced ejection fraction and iron deficiency, there was no apparent difference between ferric carboxymaltose and placebo with respect to the hierarchical composite of death, hospitalizations for heart failure, or 6-minute walk distance.
引用
收藏
页码:975 / 986
页数:12
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