Global Differences in Heart Failure With Preserved Ejection Fraction: The PARAGON-HF Trial
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, randomizované kontrolované studie, Research Support, N.I.H., Extramural, práce podpořená grantem
Grantová podpora
KL2 TR001424
NCATS NIH HHS - United States
P30 AG059988
NIA NIH HHS - United States
P30 DK092923
NIDDK NIH HHS - United States
R21 HL085375
NHLBI NIH HHS - United States
T32 HL069771
NHLBI NIH HHS - United States
- Klíčová slova
- atrial fibrillation, coronary artery disease, heart failure, prevalence, risk factors,
- MeSH
- aminobutyráty terapeutické užití MeSH
- antagonisté receptorů pro angiotenzin terapeutické užití MeSH
- bifenylové sloučeniny terapeutické užití MeSH
- celosvětové zdraví * MeSH
- dvojitá slepá metoda MeSH
- fixní kombinace léků MeSH
- hospitalizace statistika a číselné údaje MeSH
- kvalita života MeSH
- lidé MeSH
- neprilysin terapeutické užití MeSH
- rizikové faktory MeSH
- senioři MeSH
- srdeční selhání farmakoterapie mortalita patofyziologie MeSH
- tepový objem * MeSH
- valsartan terapeutické užití MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- randomizované kontrolované studie MeSH
- Research Support, N.I.H., Extramural MeSH
- Názvy látek
- aminobutyráty MeSH
- antagonisté receptorů pro angiotenzin MeSH
- bifenylové sloučeniny MeSH
- fixní kombinace léků MeSH
- neprilysin MeSH
- sacubitril and valsartan sodium hydrate drug combination MeSH Prohlížeč
- valsartan MeSH
BACKGROUND: Heart failure with preserved ejection fraction (HFpEF) is a global public health problem with important regional differences. We investigated these differences in the PARAGON-HF trial (Prospective Comparison of Angiotensin Receptor Neprilysin Inhibitor With Angiotensin Receptor Blocker Global Outcomes in HFpEF), the largest and most inclusive global HFpEF trial. METHODS: We studied differences in clinical characteristics, outcomes, and treatment effects of sacubitril/valsartan in 4796 patients with HFpEF from the PARAGON-HF trial, grouped according to geographic region. RESULTS: Regional differences in patient characteristics and comorbidities were observed: patients from Western Europe were oldest (mean 75±7 years) with the highest prevalence of atrial fibrillation/flutter (36%); Central/Eastern European patients were youngest (mean 71±8 years) with the highest prevalence of coronary artery disease (50%); North American patients had the highest prevalence of obesity (65%) and diabetes (49%); Latin American patients were younger (73±9 years) and had a high prevalence of obesity (53%); and Asia-Pacific patients had a high prevalence of diabetes (44%), despite a low prevalence of obesity (26%). Rates of the primary composite end point of total hospitalizations for HF and death from cardiovascular causes were lower in patients from Central Europe (9 per 100 patient-years) and highest in patients from North America (28 per 100 patient-years), which was primarily driven by a greater number of total hospitalizations for HF. The effect of treatment with sacubitril-valsartan was not modified by region (interaction P>0.05). CONCLUSIONS: Among patients with HFpEF recruited worldwide in PARAGON-HF, there were important regional differences in clinical characteristics and outcomes, which may have implications for the design of future clinical trials. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT01920711.
1st Faculty of Medicine Charles University Prague Czech Republic
Associazione Nazionale Medici Cardiologi Ospedalieri Florence Italy
Baylor Heart and Vascular Institute Baylor University Medical Center Dallas TX
Cardiovascular Division Brigham and Women's Hospital Harvard Medical School Boston MA
Department of Cardiology Heart Centre Rigshospitalet Copenhagen University Hospital Denmark
Department of Cardiology University Medical Centre Groningen University of Groningen the Netherlands
Department of Cardiovascular Medicine Mayo Clinic Rochester MN
Department of Medicine VA Medical Center and University of Minnesota Minneapolis
Duke NUS Medical School Singapore
Faculty of Medicine National Yang Ming University Taipei Taiwan Republic of China
Heart Failure and Research Max Super Specialty Hospital Saket New Delhi India
Inserm CIC 1433 and Université de Lorraine Centre Hospitalier Régional Universitaire Nancy France
Institut de Cardiologie de Montréal Université de Montréal QC Canada
National Heart Centre Singapore
National Research Center for Cardiology of the Ministry of Health of the Russian Federation Moscow
Novartis Pharmaceuticals Corporation East Hanover NJ
Saw Swee Hock School of Public Health National University of Singapore Singapore
Shanghai Institute of Cardiovascular Diseases Zhongshan Hospital Fudan University China
Citace poskytuje Crossref.org
ClinicalTrials.gov
NCT01920711