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Estimating the Lifetime Benefits of Treatments for Heart Failure
被引:23
|作者:
Ferreira, Joao Pedro
[1
,2
]
Docherty, Kieran F.
[1
]
Stienen, Susan
[3
]
Jhund, Pardeep S.
[1
]
Claggett, Brian L.
[4
]
Solomon, Scott D.
[4
]
Petrie, Mark C.
[1
]
Gregson, John
[5
]
Pocock, Stuart J.
[5
]
Zannad, Faiez
[2
]
McMurray, John J. V.
[1
]
机构:
[1] Univ Glasgow, BHF Cardiovasc Res Ctr, 126 Univ Pl, Glasgow G12 8TA, Lanark, Scotland
[2] Univ Lorraine, Reg Univ Hosp Nancy,INSERM U1116,Natl Inst Hlth &, French Clin Res Infrastruct Network CRIN F,Ctr Cl, Invest Network Initiat Cardiovasc & Renal Clin Tr, Nancy, France
[3] Univ Amsterdam, Amsterdam Univ Med Ctr, Amsterdam Cardiovasc Sci, Heart Ctr,Dept Clin & Expt Cardiol, Amsterdam, Netherlands
[4] Brigham & Womens Hosp, Cardiovasc Div, 75 Francis St, Boston, MA 02115 USA
[5] London Sch Hyg & Trop Med, Dept Biostat, London, England
关键词:
restricted mean survival time;
survival models;
treatment effects;
trials;
MEAN SURVIVAL-TIME;
D O I:
10.1016/j.jchf.2020.08.004
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
OBJECTIVES This study compared ways of describing treatment effects. The objective was to better explain to clinicians and patients what they might expect from a given treatment, not only in terms of relative and absolute risk reduction, but also in projections of long-term survival. BACKGROUND The restricted mean survival time (RMST) can be used to estimate of long-term survival, providing a complementary approach to more conventional metrics (e.g., absolute and relative risk), which may suggest greater benefits of therapy in high-risk patients compared with low-risk patients. METHODS Relative and absolute risk, as well as the RMST, were calculated in heart failure with reduced ejection fraction (HFrEF) trials. RESULTS As examples, in the RALES trial (more severe HFrEF), the treatment effect metrics for spironolactone versus placebo on heart failure hospitalization and/or cardiovascular death were a hazard ratio (HR) of 0.67 (95% confidence interval [CI]: 0.5 to 0.77), number needed to treat = 9 (7 to 14), and age extension of event-free survival +1.1 years (-0.1 to +2.3 years). The corresponding metrics for EMPHASIS-HF (eplerenone vs. placebo in less severe HFrEF) were 0.64 (0.54 to 0.75), 14 (1 to 22), and +2.9 (1.2 to 4.5). In patients in PARADIGM-HF aged younger than 65 years, the metrics for sacubitril/valsartan versus enalapril were 0.77 (95% CI: 0.68 to 0.88), 23 (15 to 44), and + 1.7 (0.6 to 2.8) years; for those aged 65 years or older, the metrics were 0.83 (95% CI: 0.73 to 0.94), 29 (17 to 83), and +0.9 (0.2 to 1.6) years, which provided evidence of a greater potential life extension in younger patients. Similar observations were found for lower risk patients. CONCLUSIONS RMST event-free (and overall) survival estimates provided a complementary means of evaluating the effect of therapy in relation to age and risk. They also provided a clinically useful metric that should be routinely reported and used to explain the potential long-term benefits of a given treatment, especially to younger and less symptomatic patients. (C) 2020 The Authors. Published by Elsevier on behalf of the American College of Cardiology Foundation.
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页码:984 / 995
页数:12
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