The AWAKE-HF Study: Sacubitril/Valsartan Impact on Daily Physical Activity and Sleep in Heart Failure

被引:18
|
作者
Khandwalla, Raj M. [1 ]
Grant, Daniel [2 ]
Birkeland, Kade [3 ]
Heywood, J. Thomas [4 ]
Fombu, Emmanuel [5 ,8 ]
Owens, Robert L. [6 ]
Steinhubl, Steven R. [7 ]
机构
[1] Cedars Sinai Med Care Fdn, Cedars Sinai Heart Inst, Dept Cardiol, 8501 Wilshire Ave, Beverly Hills, CA 90211 USA
[2] Novartis Pharmaceut, 1 Hlth Plaza, E Hanover, NJ 07936 USA
[3] Cedars Sinai, Dept Cardiol, 127 S San Vicente Blvd a3600, Los Angeles, CA 90048 USA
[4] Scripps Clin, Div Cardiovasc Med, 10666 N Torrey Pines Rd, San Diego, CA 92037 USA
[5] Previously Novartis Pharmaceut Corp, E Hanover, NJ USA
[6] Univ Calif San Diego, San Diego Sch Med, Div Pulm Crit Care & Sleep Med, 4520 Execut Dr, San Diego, CA 92121 USA
[7] Scripps Res Translat Sci Inst, Digital Med, 3344 North Torrey Pines Court,Suite 300, San Diego, CA 92037 USA
[8] Locust Walk Partners, 610 W 42nd St, New York, NY 10036 USA
关键词
CITY CARDIOMYOPATHY QUESTIONNAIRE; CARDIOVASCULAR-DISEASE; OLDER-ADULTS; ACTIGRAPHY; INHIBITION; PREVALENCE; NEPRILYSIN; BURDEN; APNEA;
D O I
10.1007/s40256-020-00440-y
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background AWAKE-HF evaluated the effect of the initiation of sacubitril/valsartan versus enalapril on activity and sleep using actigraphy in patients who have heart failure with reduced ejection fraction (HFrEF). Methods In this randomized, double-blind study, patients with HFrEF (n = 140) were randomly assigned to sacubitril/valsartan or enalapril for 8 weeks, followed by an 8-week open-label phase with sacubitril/valsartan. Primary endpoint was change from baseline in mean activity counts during the most active 30 min/day at week 8. The key secondary endpoint was change in mean nightly activity counts/minute from baseline to week 8. Kansas City Cardiomyopathy Questionnaire-23 (KCCQ-23) was an exploratory endpoint. Results There were no detectable differences between groups in geometric mean ratio of activity counts during the most active 30 min/day at week 8 compared with baseline (0.9456 [sacubitril/valsartan:enalapril]; 95% confidence interval [CI] 0.8863-1.0088;P = 0.0895) or in mean change from baseline in activity during sleep (difference: 2.038 counts/min; 95% CI - 0.062 to 4.138;P = 0.0570). Change from baseline to week 8 in KCCQ-23 was 2.89 for sacubitril/valsartan and 4.19 for enalapril, both nonsignificant. Conclusions In AWAKE-HF, no detectable differences in activity and sleep were observed when comparing sacubitril/valsartan with enalapril in patients with HFrEF using a wearable biosensor.
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收藏
页码:241 / 254
页数:14
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