학술논문

Clinical Effectiveness of Sacubitril/Valsartan Among Patients Hospitalized for Heart Failure With Reduced Ejection Fraction
Document Type
article
Source
Journal of the American Heart Association. 10(16)
Subject
Biomedical and Clinical Sciences
Clinical Sciences
Clinical Research
Heart Disease
Cardiovascular
Aging
Clinical Trials and Supportive Activities
Evaluation of treatments and therapeutic interventions
6.1 Pharmaceuticals
Good Health and Well Being
Aged
Aged
80 and over
Aminobutyrates
Angiotensin II Type 1 Receptor Blockers
Biphenyl Compounds
Drug Combinations
Female
Heart Failure
Hospitalization
Humans
Male
Medicare
Neprilysin
Patient Discharge
Protease Inhibitors
Registries
Risk Assessment
Risk Factors
Stroke Volume
Time Factors
Treatment Outcome
United States
Valsartan
Ventricular Function
Left
heart failure
reduced ejection fraction
registry
sacubitril
valsartan
sacubitril/valsartan
Cardiorespiratory Medicine and Haematology
Cardiovascular medicine and haematology
Language
Abstract
Background Sacubitril/Valsartan has been highly efficacious in randomized trials of heart failure with reduced ejection fraction (HFrEF). However, the effectiveness of sacubitril/valsartan in older patients hospitalized for HFrEF in real-world US practice is unclear. Methods and Results This study included Medicare beneficiaries age ≥65 years who were hospitalized for HFrEF ≤40% in the Get With The Guidelines-Heart Failure registry between October 2015 and December 2018, and eligible for sacubitril/valsartan. Associations between discharge prescription of sacubitril/valsartan and clinical outcomes were assessed after inverse probability of treatment weighting and adjustment for other HFrEF medications. Overall, 1551 (10.9%) patients were discharged on sacubitril/valsartan. Of those not prescribed sacubitril/valsartan, 7857 (62.0%) were prescribed an angiotensin-converting enzyme inhibitor/angiotensin II receptor blocker. Over 12-month follow-up, compared with a discharge prescription of angiotensin-converting enzyme inhibitor/angiotensin II receptor blocker, sacubitril/valsartan was independently associated with lower all-cause mortality (adjusted hazard ratio [HR], 0.82; 95% CI, 0.72-0.94; P=0.004) but not all-cause hospitalization (adjusted HR, 0.97; 95% CI, 0.89-1.07; P=0.55) or heart failure hospitalization (adjusted HR, 1.04; 95% CI, 0.91-1.18; P=0.59). Patients prescribed sacubitril/valsartan versus those without a prescription had lower risk of all-cause mortality (adjusted HR, 0.69; 95% CI, 0.60-0.79; P