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Heart failure with preserved ejection fraction.
Hamo, Carine E; DeJong, Colette; Hartshorne-Evans, Nick; Lund, Lars H; Shah, Sanjiv J; Solomon, Scott; Lam, Carolyn S P.
Afiliação
  • Hamo CE; New York University School of Medicine, Leon H. Charney Division of Cardiology, New York University Langone Health, New York, NY, USA.
  • DeJong C; Division of Cardiology, University of California San Francisco, San Francisco, CA, USA.
  • Hartshorne-Evans N; CEO and Founder of the Pumping Marvellous Foundation (Patient-Led Heart Failure Charity), Preston, UK.
  • Lund LH; Unit of Cardiology, Department of Medicine, Karolinska Institutet, and Heart and Vascular Theme, Karolinska University Hospital, Stockholm, Sweden.
  • Shah SJ; Division of Cardiology, Department of Medicine and Bluhm Cardiovascular Institute Northwestern University Feinberg School of Medicine Chicago, Chicago, IL, USA.
  • Solomon S; Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • Lam CSP; National Heart Centre Singapore & Duke-National University of Singapore, Singapore, Singapore. Carolyn.lam@duke-nus.edu.sg.
Nat Rev Dis Primers ; 10(1): 55, 2024 Aug 14.
Article em En | MEDLINE | ID: mdl-39143132
ABSTRACT
Heart failure with preserved ejection fraction (HFpEF) accounts for nearly half of all heart failure cases and has a prevalence that is expected to rise with the growing ageing population. HFpEF is associated with significant morbidity and mortality. Specific HFpEF risk factors include age, diabetes, hypertension, obesity and atrial fibrillation. Haemodynamic contributions to HFpEF include changes in left ventricular structure, diastolic and systolic dysfunction, left atrial myopathy, pulmonary hypertension, right ventricular dysfunction, chronotropic incompetence, and vascular dysfunction. Inflammation, fibrosis, impaired nitric oxide signalling, sarcomere dysfunction, and mitochondrial and metabolic defects contribute to the cellular and molecular changes observed in HFpEF. HFpEF impacts multiple organ systems beyond the heart, including the skeletal muscle, peripheral vasculature, lungs, kidneys and brain. The diagnosis of HFpEF can be made in individuals with signs and symptoms of heart failure with abnormality in natriuretic peptide levels or evidence of cardiopulmonary congestion, facilitated by the use of HFpEF risk scores and additional imaging and testing with the exclusion of HFpEF mimics. Management includes initiation of guideline-directed medical therapy and management of comorbidities. Given the significant impact of HFpEF on quality of life, future research efforts should include a particular focus on how patients can live better with this disease.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Volume Sistólico / Insuficiência Cardíaca Limite: Humans Idioma: En Revista: Nat Rev Dis Primers Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Volume Sistólico / Insuficiência Cardíaca Limite: Humans Idioma: En Revista: Nat Rev Dis Primers Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Reino Unido