Sacubitril/valsartan and loop diuretic requirement in heart failure with preserved ejection fraction in the PARAGON-HF trial

被引:21
作者
Chatur, Safia [1 ]
Claggett, Brian L. [1 ]
Vardeny, Orly [2 ]
Jering, Karola [1 ]
Desai, Akshay S. [1 ]
Pfeffer, Marc A. [1 ]
Lefkowitz, Martin [3 ]
McMurray, John J., V [4 ]
Solomon, Scott D. [1 ]
Vaduganathan, Muthiah [1 ]
机构
[1] Harvard Med Sch, Brigham & Womens Hosp, Cardiovasc Div, Boston, MA 02115 USA
[2] Univ Minnesota, Minneapolis VA Ctr Care Delivery & Outcomes Res, Minneapolis, MN USA
[3] Novartis Pharmaceut, E Hanover, NJ USA
[4] Univ Glasgow, BHF Cardiovasc Res Ctr, Glasgow, Lanark, Scotland
关键词
Heart failure with preserved ejection fraction; Sacubitril; valsartan; Diuretics; OUTCOMES;
D O I
10.1002/ejhf.2703
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims As sacubitril/valsartan may potentiate early natriuresis, expert consensus documents recommend diuretic dose reduction on first initiation. However, there are limited data on the effects of sacubitril/valsartan on the background of varying diuretic regimens or on diuretic requirements over time in heart failure (HF) with preserved ejection fraction (HFpEF). Methods and results In this post hoc analysis of PARAGON-HF, of the 4796 patients, background diuretic therapy was distributed as follows: 341 (7%) on no diuretic, 698 (15%) on non-loop diuretic, and 3757 (78%) were on loop diuretics (1255, 1589, and 913 were on <40, 40 and >40 mg furosemide equivalent doses, respectively). The primary composite outcome of total HF hospitalizations and cardiovascular death was analysed using semiparametric proportional rates methods. The cumulative incidence of the primary composite outcome (first events) was lowest in patients on no diuretic and highest in those on >40 mg of loop diuretic (p < 0.001). The effects of sacubitril/valsartan (vs. valsartan) on the primary composite outcome (recurrent events) did not significantly vary by baseline diuretic use (p(interaction) = 0.65). Treatment effects on safety outcomes were similar across diuretic categories. Sacubitril/valsartan reduced new loop diuretic initiations over the course of the trial (hazard ratio 0.83; 95% confidence interval 0.68-1.00, p = 0.055), with similar mean loop diuretic dose and rates of diuretic discontinuation between treatment groups in follow-up. Patients randomized to sacubitril/valsartan experienced a slight early reduction in diuretic initiation or dose escalation at 30 days after initiation (net reduction 1.7%, p = 0.02), but these differences were not sustained beyond this timepoint. Conclusions Patients with HFpEF on higher baseline diuretic doses were at heightened risk of HF events, but similarly benefited from sacubitril/valsartan with a consistent safety profile across a range of diuretic doses. Initiation of sacubitril/valsartan was associated with modestly lower new loop diuretic requirement in follow-up.
引用
收藏
页码:87 / 94
页数:8
相关论文
共 17 条
[1]   Diuretic dose and long-term outcomes in elderly patients with heart failure after hospitalization [J].
Abdel-Qadir, Husam M. ;
Tu, Jack V. ;
Yun, Lingsong ;
Austin, Peter C. ;
Newton, Gary E. ;
Lee, Douglas S. .
AMERICAN HEART JOURNAL, 2010, 160 (02) :264-U80
[2]   Relation of loop diuretic dose to mortality in advanced heart failure [J].
Eshaghian, Shervin ;
Horwich, Tamara B. ;
Fonarow, Gregg C. .
AMERICAN JOURNAL OF CARDIOLOGY, 2006, 97 (12) :1759-1764
[3]   Relation between dose of loop diuretics and outcomes in a heart failure population: Results of the ESCAPE Trial [J].
Hasselblad, Vic ;
Stough, Wendy Gattis ;
Shah, Monica R. ;
Lokhnygina, Yuliya ;
O'Connor, Christopher M. ;
Califf, Robert M. ;
Adams, Kirkwood F., Jr. .
EUROPEAN JOURNAL OF HEART FAILURE, 2007, 9 (10) :1064-1069
[4]   Diuretic and renal effects of spironolactone and heart failure hospitalizations: aTOPCATAmericas analysis [J].
Kalogeropoulos, Andreas P. ;
Thankachen, Jincy ;
Butler, Javed ;
Fang, James C. .
EUROPEAN JOURNAL OF HEART FAILURE, 2020, 22 (09) :1600-1610
[5]   Semiparametric regression for the mean and rate functions of recurrent events [J].
Lin, DY ;
Wei, LJ ;
Yang, I ;
Ying, Z .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 2000, 62 :711-730
[6]  
McDonagh Theresa A, 2022, Rev Esp Cardiol (Engl Ed), V75, P523, DOI [10.1093/eurheartj/ehab368, 10.1002/ejhf.2333, 10.1016/j.rec.2022.05.005]
[7]   Hospitalisation in Patients With Heart Failure With Preserved Ejection Fraction [J].
Nanayakkara, Shane ;
Patel, Hitesh C. ;
Kaye, David M. .
CLINICAL MEDICINE INSIGHTS-CARDIOLOGY, 2018, 12
[8]   Sacubitril-Valsartan, Clinical Benefits and Related Mechanisms of Action in Heart Failure With Reduced Ejection Fraction. A Review [J].
Pascual-Figal, Domingo ;
Bayes-Genis, Antoni ;
Beltran-Troncoso, Paola ;
Caravaca-Perez, Pedro ;
Conde-Martel, Alicia ;
Crespo-Leiro, Maria G. ;
Delgado, Juan F. ;
Diez, Javier ;
Formiga, Francesc ;
Manito, Nicolas .
FRONTIERS IN CARDIOVASCULAR MEDICINE, 2021, 8
[9]   Sacubitril-Valsartan in a routine community population: attention to volume status critical to achieving target dose [J].
Pharithi, Rebabonye B. ;
Ferre-Vallverdu, Maria ;
Maisel, Alan S. ;
O'Connell, Eoin ;
Walshe, Myra ;
Sweeney, Claire ;
Barton, James ;
McDonald, Kathrine ;
O'Hare, Daniel ;
Watson, Chris ;
Gallagher, Joe ;
Ledwidge, Mark ;
McDonald, Kenneth .
ESC HEART FAILURE, 2020, 7 (01) :159-167
[10]   Heart Failure with Preserved Ejection Fraction [J].
Redfield, Margaret M. .
NEW ENGLAND JOURNAL OF MEDICINE, 2016, 375 (19) :1868-1877