Efficacy and Safety of Spironolactone in Patients With HFpEF and Chronic Kidney Disease

被引:71
|
作者
Beldhuis, Iris E. [1 ,2 ]
Myhre, Peder L. [1 ]
Claggett, Brian [1 ]
Damman, Kevin [2 ]
Fang, James C. [3 ]
Lewis, Eldrin F. [1 ]
O'Meara, Eileen [4 ]
Pitt, Bertram [5 ]
Shah, Sanjiv J. [6 ]
Voors, Adriaan A. [2 ]
Pfeffer, Marc A. [1 ]
Solomon, Scott D. [1 ]
Desai, Akshay S. [1 ]
机构
[1] Brigham & Womens Hosp, Dept Med, Cardiovasc Div, 75 Francis St, Boston, MA 02115 USA
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Cardiol, Groningen, Netherlands
[3] Univ Utah, Div Cardiovasc Med, Sch Med, Salt Lake City, UT USA
[4] Montreal Heart Inst, Dept Med, Montreal, PQ, Canada
[5] Univ Michigan, Sch Med, Dept Internal Med, Ann Arbor, MI USA
[6] Northwestern Univ, Dept Med, Div Cardiol, Feinberg Sch Med, Chicago, IL 60611 USA
基金
美国国家卫生研究院;
关键词
chronic kidney disease; heart failure with preserved ejection fraction; renal function; safety; spironolactone; HEART-FAILURE; RENAL-FUNCTION; INSUFFICIENCY; OUTCOMES; HYPERKALEMIA; PREDICTOR; SURVIVAL;
D O I
10.1016/j.jchf.2018.10.017
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES This study investigated the association between baseline renal function and the net benefit of spironolactone in patients with heart failure (HF) with a preserved ejection fraction (HFpEF). BACKGROUND Guidelines recommend consideration of spironolactone to reduce HF hospitalization in HFpEF. However, spironolactone may increase risk for hyperkalemia and worsening renal function, particularly in patients with chronic kidney disease. METHODS This investigation analyzed data from patients enrolled in the TOPCAT (Treatment of Preserved Cardiac Function Heart Failure With an Aldosterone Antagonist Trial) Americas study (N = 1,767) to examine the association between the baseline estimated glomerular filtration rate (eGFR) and the primary composite outcome of cardiovascular death, HF hospitalization, or aborted cardiac arrest, as well as safety outcomes, including hyperkalemia, worsening renal function, and permanent drug discontinuation for adverse events (AEs). Variations in the efficacy and safety of spironolactone according to eGFR were examined in Cox models using interaction terms. RESULTS The incidence of both the primary outcome and drug-related AEs increased with declining eGFR. Compared with placebo, across all eGFR categories, spironolactone was associated with lower relative risk for the primary efficacy outcome and for hypokalemia, but higher relative risk for hyperkalemia, worsening renal function, and drug discontinuation. During 4-year follow-up, the absolute risk for AEs that prompted drug discontinuation was amplified in the lower eGFR categories, which suggested heightened risk for drug intolerance with declining renal function. CONCLUSIONS Although consistent efficacy of spironolactone was observed across the range of eGFR, the risk of AEs was amplified in the lower eGFR categories. These data supported use of spironolactone to treat HFpEF patients with advanced chronic kidney disease only when close laboratory surveillance is possible. (C) 2019 by the American College of Cardiology Foundation.
引用
收藏
页码:25 / 32
页数:8
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