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The AWAKE-HF Study: Sacubitril/Valsartan Impact on Daily Physical Activity and Sleep in Heart Failure.
Khandwalla, Raj M; Grant, Daniel; Birkeland, Kade; Heywood, J Thomas; Fombu, Emmanuel; Owens, Robert L; Steinhubl, Steven R.
Afiliación
  • Khandwalla RM; Department of Cardiology, Cedars-Sinai Medical Care Foundation, Cedars-Sinai Heart Institute, 8501 Wilshire Ave, Beverly Hills, California, 90211, United States. Raj.Khandwalla@cshs.org.
  • Grant D; Novartis Pharmaceuticals Corporation, 1 Health Plaza, East Hanover, NJ, 07936, USA.
  • Birkeland K; Department of Cardiology, Cedars-Sinai, 127 S San Vicente Blvd a3600, Los Angeles, CA, 90048, USA.
  • Heywood JT; Division of Cardiovascular Medicine, Scripps Clinic, 10666 N Torrey Pines Rd, San Diego, CA, 92037, USA.
  • Fombu E; Previously Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
  • Owens RL; Locust Walk Partners, 610 W 42nd St., New York, NY, 10036, USA.
  • Steinhubl SR; Division of Pulmonary, Critical Care, and Sleep Medicine, San Diego School of Medicine, University of California, 4520 Executive Drive, San Diego, CA, 92121, USA.
Am J Cardiovasc Drugs ; 21(2): 241-254, 2021 Mar.
Article en En | MEDLINE | ID: mdl-32978755
ABSTRACT

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/valsartanenalapril]; 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. CLINICAL TRIAL REGISTRATION ClinicalTrials.gov, NCT02970669.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Sueño / Compuestos de Bifenilo / Enalapril / Ejercicio Físico / Antagonistas de Receptores de Angiotensina / Valsartán / Aminobutiratos / Insuficiencia Cardíaca Tipo de estudio: Clinical_trials Idioma: En Revista: Am J Cardiovasc Drugs Asunto de la revista: ANGIOLOGIA / CARDIOLOGIA / TERAPIA POR MEDICAMENTOS Año: 2021 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Sueño / Compuestos de Bifenilo / Enalapril / Ejercicio Físico / Antagonistas de Receptores de Angiotensina / Valsartán / Aminobutiratos / Insuficiencia Cardíaca Tipo de estudio: Clinical_trials Idioma: En Revista: Am J Cardiovasc Drugs Asunto de la revista: ANGIOLOGIA / CARDIOLOGIA / TERAPIA POR MEDICAMENTOS Año: 2021 Tipo del documento: Article