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Atrial Fibrillation and Dapagliflozin Efficacy in Patients With Preserved or Mildly Reduced Ejection Fraction.
Butt, Jawad H; Kondo, Toru; Jhund, Pardeep S; Comin-Colet, Josep; de Boer, Rudolf A; Desai, Akshai S; Hernandez, Adrian F; Inzucchi, Silvio E; Janssens, Stefan P; Kosiborod, Mikhail N; Lam, Carolyn S P; Langkilde, Anna Maria; Lindholm, Daniel; Martinez, Felipe; Petersson, Magnus; Shah, Sanjiv J; Thierer, Jorge; Vaduganathan, Muthiah; Verma, Subodh; Wilderäng, Ulrica; Claggett, Brian C; Solomon, Scott D; McMurray, John J V.
Afiliação
  • Butt JH; British Heart Foundation Cardiovascular Research Centre, University of Glasgow, Glasgow, United Kingdom; Department of Cardiology, Rigshospitalet Copenhagen University Hospital, Copenhagen, Denmark.
  • Kondo T; British Heart Foundation Cardiovascular Research Centre, University of Glasgow, Glasgow, United Kingdom.
  • Jhund PS; British Heart Foundation Cardiovascular Research Centre, University of Glasgow, Glasgow, United Kingdom.
  • Comin-Colet J; Cardiology Department, Bellvitge University Hospital, Bio-Heart (IDIBELL), University of Barcelona, Hospitalet de Llobregat, Barcelona, Spain.
  • de Boer RA; University of Groningen, Groningen, the Netherlands.
  • Desai AS; Division of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA.
  • Hernandez AF; Duke University Medical Center, Durham, North Carolina, USA.
  • Inzucchi SE; Yale School of Medicine, New Haven, Connecticut, USA.
  • Janssens SP; Cardiac Intensive Care, Department of Cardiovascular Diseases, University Hospitals Leuven, Leuven, Belgium.
  • Kosiborod MN; Saint Luke's Mid America Heart Institute, Kansas City, Missouri, USA.
  • Lam CSP; National Heart Centre Singapore and Duke-National University of Singapore, Singapore.
  • Langkilde AM; Late-Stage Development, Cardiovascular, Renal, and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
  • Lindholm D; Late-Stage Development, Cardiovascular, Renal, and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
  • Martinez F; University of Cordoba, Cordoba, Argentina.
  • Petersson M; Late-Stage Development, Cardiovascular, Renal, and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
  • Shah SJ; Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
  • Thierer J; Jefe de Unidad de Insuficiencia Cardíaca, Centro de Educación Médica e Investigaciones Clínicas Norberto Quirno (CEMIC), Buenos Aires, Argentina.
  • Vaduganathan M; Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Verma S; Division of Cardiac Surgery, St Michael's Hospital, University of Toronto, Toronto, Ontario, Canada.
  • Wilderäng U; Late-Stage Development, Cardiovascular, Renal, and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
  • Claggett BC; Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Solomon SD; Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • McMurray JJV; British Heart Foundation Cardiovascular Research Centre, University of Glasgow, Glasgow, United Kingdom. Electronic address: john.mcmurray@glasgow.ac.uk.
J Am Coll Cardiol ; 80(18): 1705-1717, 2022 11 01.
Article em En | MEDLINE | ID: mdl-36041668
ABSTRACT

BACKGROUND:

Atrial fibrillation (AF) is common in heart failure (HF), is associated with worse outcomes compared with sinus rhythm, and may modify the effects of therapy.

OBJECTIVES:

This study examined the effects of dapagliflozin according to the presence or not of AF in the DELIVER (Dapagliflozin Evaluation to Improve the LIVEs of Patients With PReserved Ejection Fraction Heart Failure) trial.

METHODS:

A total of 6,263 patients with HF with New York Heart Association functional class II-IV, left ventricular ejection fraction >40%, evidence of structural heart disease, and elevated N-terminal pro-B-type natriuretic peptide levels were randomized to dapagliflozin or placebo. Clinical outcomes and the effect of dapagliflozin, according to AF status, were examined. The primary outcome was a composite of cardiovascular death or worsening HF.

RESULTS:

Of the 6,261 patients with data on baseline AF, 43.3% had no AF, 18.0% had paroxysmal AF, and 38.7% had persistent/permanent AF. The risk of the primary endpoint was higher in patients with AF, especially paroxysmal AF, driven by a higher rate of HF hospitalization no AF, HF hospitalization rate per 100 person-years (4.5 [95% CI 4.0-5.1]), paroxysmal AF (7.5 [95% CI 6.4-8.7]), and persistent/permanent AF (6.4 [95% CI 5.7-7.1]) (P < 0.001). The benefit of dapagliflozin on the primary outcome was consistent across AF types no AF, HR 0.89 (95% CI 0.74-1.08); paroxysmal AF, HR 0.75 (95% CI 0.58-0.97); persistent/permanent AF, HR 0.79 (95% CI 0.66-0.95) (Pinteraction = 0.49). Consistent effects were observed for HF hospitalization, cardiovascular death, all-cause mortality, and improvement in the KCCQ-TSS.

CONCLUSIONS:

In DELIVER, the beneficial effects of dapagliflozin compared with placebo on clinical events and symptoms were consistent, irrespective of type of AF at baseline. (Dapagliflozin Evaluation to Improve the LIVEs of Patients With PReserved Ejection Fraction Heart Failure. [DELIVER]; NCT03619213).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fibrilação Atrial / Disfunção Ventricular Esquerda / Insuficiência Cardíaca Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fibrilação Atrial / Disfunção Ventricular Esquerda / Insuficiência Cardíaca Idioma: En Ano de publicação: 2022 Tipo de documento: Article