Sacubitril/valsartan versus valsartan initiation in patients naïve to renin-angiotensin system inhibitors: Insights from PARAGLIDE-HF

被引:0
作者
Nouhravesh, Nina [1 ,2 ]
Gunn, Alexander H. [1 ]
Cyr, Derek [1 ]
Hernandez, Adrian F. [1 ]
Morrow, David A. [3 ]
Velazquez, Eric J. [4 ]
Ward, Jonathan H. [5 ]
Sarwat, Samiha [5 ]
Sharma, Kavita [6 ]
Williamson, Kristin M. [5 ]
Starling, Randall C. [7 ]
Lepage, Serge [8 ]
Zieroth, Shelley [9 ]
Solomon, Scott D. [3 ]
Mentz, Robert J. [1 ]
机构
[1] Duke Clin Res Inst, 300 W Morgan St, Durham, NC 2770 USA
[2] Herlev Gentofte Univ Hosp, Dept Cardiol, Copenhagen, Denmark
[3] Harvard Med Sch, Brigham & Womens Hosp, Boston, MA USA
[4] Yale Sch Med, New Haven, CT USA
[5] Novartis Pharmaceut, E Hanover, NJ USA
[6] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
[7] Cleveland Clin, Dept Cardiovasc Med, Cleveland, OH USA
[8] Univ Sherbrooke, Quebec City, PQ, Canada
[9] Univ Manitoba, Winnipeg, MB, Canada
关键词
Acute decompensated HFpEF; Clinical outcomes; HFmrEF; Natriuretic peptides; Sacubitril/valsartan; HEART-FAILURE;
D O I
10.1002/ejhf.3579
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims Whether prior treatment with angiotensin-converting enzyme inhibitors (ACEi) or angiotensin receptor blockers (ARBs) modifies efficacy and safety of sacubitril/valsartan (Sac/Val) in patients with heart failure (HF) and ejection fraction (EF) >40% is unclear, thus Sac/Val according to ACEi/ARB status at baseline was assessed. Methods and results This was a pre-specified analysis of Prospective comparison of ARNI with ARB Given following stabiLization In DEcompensated HFpEF (PARAGLIDE-HF), a double-blind, randomized controlled trial of Sac/Val versus valsartan, categorizing patients according to baseline ACEi/ARB status. The primary endpoint was time-averaged proportional change in N-terminal pro-B-type natriuretic peptide (NT-proBNP) from baseline through weeks 4 and 8. Secondary analyses included a win-ratio analysis of the hierarchical outcome of (i) cardiovascular death; (ii) HF hospitalizations; (iii) urgent HF visits; and (iv) time-averaged proportional change in NT-proBNP from baseline to weeks 4 and 8, in addition to safety outcomes. Among 466 patients, 107 (23%) were ACEi/ARB na & iuml;ve at the time of randomization. NT-proBNP favoured Sac/Val irrespective of ACEi/ARB status (na & iuml;ve: 0.76, 95% confidence interval [CI] 0.51-1.13; users: 0.88, 95% CI 0.74-1.05; pinteraction = 0.52). The win ratio of the hierarchical outcome was 1.13 (95% CI 0.86-1.49) for ACEi/ARB users and 1.38 (95% CI 0.81-2.37) for ACEi/ARB na & iuml;ve (pinteraction = 0.51). Safety endpoints showed non-significant interactions by ACEi/ARB status, with odds ratio of 1.79 (95% CI 0.68-4.72) and 0.71 (95% CI 0.29-1.78) for symptomatic hypotension and worsening renal function, respectively for ACEi/ARB na & iuml;ve. Conclusion In HF with EF >40% stabilized after worsening HF, safety and efficacy were similar irrespective of ACEi/ARB status at baseline, supporting early initiation irrespective of prior ACEi/ARB use.
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页数:8
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