Your browser doesn't support javascript.
loading
Phenogroups and Their Prognosis of Acute Decompensated Heart Failure with Preserved Ejection Fraction.
Makino, Taro; Ishihara, Yuya; Harada, Masahide; Sobue, Yoshihiro; Watanabe, Eiichi; Ozaki, Yukio; Izawa, Hideo.
Afiliação
  • Makino T; Department of Cardiology, Hekinan City Hospital.
  • Ishihara Y; Department of Laboratory Medicine, Fujita Health University Hospital.
  • Harada M; Department of Cardiology, Fujita Health University Hospital.
  • Sobue Y; Division of Cardiology, Department of Internal Medicine, Fujita Health University Bantane Hospital.
  • Watanabe E; Division of Cardiology, Department of Internal Medicine, Fujita Health University Bantane Hospital.
  • Ozaki Y; Division of Cardiology, Department of Internal Medicine, Fujita Health University Okazaki Medical Center.
  • Izawa H; Department of Cardiology, Fujita Health University Hospital.
Int Heart J ; 65(5): 841-848, 2024 Sep 30.
Article em En | MEDLINE | ID: mdl-39261030
ABSTRACT
Acute heart failure is an important cause of unplanned hospitalizations and poses a significant burden through increased mortality and frequent hospitalizations. Heart failure with preserved ejection fraction (HFpEF) presents as a diverse condition characterized by complex cardiovascular and non-cardiovascular pathology. This study aimed to identify distinct clinical phenotypes in acute decompensated HFpEF (ADHF) using cluster analysis and assess their prognostic significance. We applied a latent class analysis to 1,281 ADHF patients admitted to a single cardiac intensive care unit between 2008 and 2022 with a left ventricular ejection fraction ≥ 50%. We used 83 factors obtained at hospitalization. We evaluated the association between phenogroups and clinical outcomes using either Cox regression model or Fine-Gray competing risk model. We identified 4 phenogroups Phenogroup 1 (n = 133, 10%) included younger patients with metabolic disorders and a low level of B-type natriuretic peptide (BNP); Phenogroup 2 (n = 346, 27%) had systemic congestion and high BNP levels; Phenogroup 3 (n = 514, 40%) had multiple comorbidities and vascular disorders; Phenogroup 4 (n = 288, 22%) included older patients with bradyarrhythmia and atrial fibrillation. After adjusting for age, sex, and Get with the Guidelines-Heart Failure risk score, Phenogroup 2 had the highest risk of all-cause death and cardiac death. In conclusion, we identified 4 clinically relevant phenogroups of ADHF patients, each associated with different adverse outcomes. Phenotyping may provide a better understanding of the underlying mechanisms involved in the heterogeneity of ADHF and decompensation. Furthermore, it may facilitate the search for phenotype-specific therapeutic strategies.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Volume Sistólico / Insuficiência Cardíaca Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Volume Sistólico / Insuficiência Cardíaca Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article