Estimated Long-Term Benefit of Dapagliflozin in Patients With Heart Failure

被引:12
|
作者
Vaduganathan, Muthiah [1 ]
Claggett, Brian L. [1 ]
Jhund, Pardeep [2 ]
de Boer, Rudolf A. [3 ]
Hernandez, Adrian F. [4 ]
Inzucchi, Silvio E. [5 ]
Kosiborod, Mikhail N. [6 ]
Lam, Carolyn S. P. [7 ,8 ]
Martinez, Felipe [9 ]
Shah, Sanjiv J. [10 ]
Desai, Akshay S. [1 ]
Lindholm, Daniel [11 ]
Petersson, Magnus [11 ]
Langkilde, Anna Maria [11 ]
McMurray, John J., V [2 ]
Solomon, Scott D. [1 ]
机构
[1] Harvard Med Sch, Brigham & Womens Hosp, Cardiovasc Div, 75 Francis St, Boston, MA 02115 USA
[2] Univ Glasgow, British Heart Fdn, Glasgow, Lanark, Scotland
[3] Univ Groningen, Groningen, Netherlands
[4] Duke Univ, Med Ctr, Durham, NC USA
[5] Yale Sch Med, New Haven, CT USA
[6] St Lukes Mid Amer Heart Inst, Kansas City, MO USA
[7] Natl Heart Ctr Singapore, Singapore, Singapore
[8] Duke Natl Univ Singapore, Singapore, Singapore
[9] Univ Nacl Cordoba, Cordoba, Argentina
[10] Northwestern Univ, Feinberg Sch Med, Chicago, IL 60611 USA
[11] AstraZeneca, Gothenburg, Sweden
基金
美国国家卫生研究院; 英国医学研究理事会;
关键词
KEY WORDS heart failure with mildly reduced ejection fraction; heart failure with preserved ejection fraction; implementation science; modeling; sodium-glucose cotransporter-2 inhibitors; LIFE EXPECTANCY; SURVIVAL;
D O I
10.1016/j.jacc.2022.08.745
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Recent guidelines support consideration of sodium-glucose cotransporter-2 inhibitors in the long-term management of heart failure (HF) with mildly reduced or preserved ejection fraction. Patients and clinicians may be interested in the expected lifetime benefits of sodium-glucose cotransporter-2 inhibitors in this population.OBJECTIVES This study aimed to estimate event-free survival gains from long-term use of dapagliflozin in patients with HF with mildly reduced or preserved ejection fraction overall and in clinically relevant subgroups.METHODS In this prespecified analysis of DELIVER (Dapagliflozin Evaluation to Improve the Lives of Patients With Preserved Ejection Fraction Heart Failure), we applied validated nonparametric age-based methods to extrapolate potential gains in survival free from the primary endpoint (cardiovascular death or worsening HF event) from long-term use of dapagliflozin. Eligible participants had symptomatic HF, left ventricular ejection fraction >40%, elevated natriuretic peptide levels, and structural heart disease. For every year between the ages of 55 and 85 years, we estimated event-free survival using age at randomization rather than time from randomization as the time horizon. Residual lifespan free from a primary endpoint was estimated based on area under the survival curve in each arm.RESULTS Among 6,263 participants, mean survival free from the primary endpoint for a 65-year-old participant was 12.1 years (95% CI: 11.0-13.2 years) with dapagliflozin and 9.7 years (95% CI: 8.8-10.7 years) with placebo, representing a 2.3-year (95% CI: 0.9-3.8 years) event-free survival gain (P 1/4 0.002). Treatment gains in survival free from the primary endpoint ranged from 2.0 years (95% CI: -0.6 to 4.6 years) in a 55-year-old to 1.2 years (95% CI: -0.1 to 2.4 years) in a 75-year-old patient. Mean event-free survival was greater with dapagliflozin than with placebo across all 14 subgroups. CONCLUSIONS Treatment with dapagliflozin is projected to extend event-free survival by up to 2.0 to 2.5 years among middle-aged and older individuals with HF with mildly reduced or preserved ejection fraction. (DELIVER [Dapagliflozin Evaluation to Improve the Lives of Patients With Preserved Ejection Fraction Heart Failure]; NCT03619213) (J Am Coll Cardiol 2022;80:1775-1784)(c) 2022 The Authors. Published by Elsevier on behalf of the American College of Cardiology Foundation. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:1775 / 1784
页数:10
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