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Patient Characteristics, Outcomes, and Effects of Dapagliflozin According to the Duration of Heart Failure: A Prespecified Analysis of the DELIVER Trial.
Kondo, Toru; Jering, Karola S; Borleffs, C Jan Willem; de Boer, Rudolf A; Claggett, Brian L; Desai, Akshay S; Dobreanu, Dan; Inzucchi, Silvio E; Hernandez, Adrian F; Janssens, Stefan P; Jhund, Pardeep S; Kosiborod, Mikhail N; Lam, Carolyn S P; Langkilde, Anna Maria; Martinez, Felipe A; Petersson, Magnus; Vinh, Pham Nguyen; Vaduganathan, Muthiah; Solomon, Scott D; McMurray, John J V.
Afiliação
  • Kondo T; British Heart Foundation Cardiovascular Research Centre, University of Glasgow, UK (T.K., P.S.J., J.J.V.M.).
  • Jering KS; Department of Cardiology, Nagoya University Graduate School of Medicine, Japan (T.K.).
  • Borleffs CJW; Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA (K.S.J., B.L.C., A.S.D., M.V., S.D.S.).
  • de Boer RA; Haga Teaching Hospital, the Hague, the Netherlands (C.J.W.B.).
  • Claggett BL; Erasmus Medical Center, Rotterdam, the Netherlands (R.A.d.B.).
  • Desai AS; Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA (K.S.J., B.L.C., A.S.D., M.V., S.D.S.).
  • Dobreanu D; Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA (K.S.J., B.L.C., A.S.D., M.V., S.D.S.).
  • Inzucchi SE; University of Medicine, Pharmacy, Science and Technology "G.E. Palade," Târgu Mureș, Romania (D.D.).
  • Hernandez AF; Yale School of Medicine and Yale-New Haven Hospital, CT (S.E.I.).
  • Janssens SP; Duke University Medical Center, Durham, NC (A.F.H.).
  • Jhund PS; Cardiac Intensive Care, Department of Cardiovascular Diseases, University Hospitals Leuven, Belgium (S.P.J.).
  • Kosiborod MN; British Heart Foundation Cardiovascular Research Centre, University of Glasgow, UK (T.K., P.S.J., J.J.V.M.).
  • Lam CSP; Saint Luke's Mid America Heart Institute, University of Missouri-Kansas City, Kansas City, MO (M.N.K.).
  • Langkilde AM; National Heart Centre Singapore & Duke-National University of Singapore (C.S.P.L.).
  • Martinez FA; Late-Stage Development, Cardiovascular, Renal, and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden (A.M.L., M.P.).
  • Petersson M; University of Cordoba, Argentina (F.A.M.).
  • Vinh PN; Late-Stage Development, Cardiovascular, Renal, and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden (A.M.L., M.P.).
  • Vaduganathan M; Cardiovascular Center, Tam Anh hospital, Tan Tao University, Vietnam (P.N.V.).
  • Solomon SD; Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA (K.S.J., B.L.C., A.S.D., M.V., S.D.S.).
  • McMurray JJV; Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA (K.S.J., B.L.C., A.S.D., M.V., S.D.S.).
Circulation ; 147(14): 1067-1078, 2023 04 04.
Article em En | MEDLINE | ID: mdl-36876483
BACKGROUND: How patient characteristics and outcomes vary according to the duration of heart failure (HF) is unknown in individuals with mildly reduced or preserved ejection fraction. We compared these, and the efficacy and safety of dapagliflozin, according to the time from diagnosis of HF in a prespecified analysis of the DELIVER trial (Dapagliflozin Evaluation to Improve the Lives of Patients With Preserved Ejection Fraction Heart Failure). METHODS: HF duration was categorized as ≤6 months, >6 to 12 months, >1 to 2 years, >2 to 5 years, or >5 years. The primary outcome was the composite of worsening HF or cardiovascular death. The effect of treatment was examined by HF duration category. RESULTS: The number of patients in each category was as follows: 1160 (≤6 months), 842 (>6 to 12 months), 995 (>1 to 2 years), 1569 (>2 to 5 years), and 1692 (>5 years). Patients with longer-duration HF were older and had more comorbidities with worse symptoms. The rate of the primary outcome (per 100 person-years) increased with HF duration: ≤6 months, 7.3 (95% CI, 6.3 to 8.4); >6 to 12 months, 7.1 (6.0 to 8.5); >1 to 2 years, 8.4 (7.2 to 9.7); >2 to 5 years, 8.9 (7.9 to 9.9); and >5 years, 10.6 (9.5 to 11.7). Similar trends were seen for other outcomes. The benefit of dapagliflozin was consistent across HF duration category: the hazard ratio for the primary outcome in the ≤6-month group was 0.67 (95% CI, 0.50 to 0.91); >6 to 12 months, 0.78 (0.55 to 1.12); >1 to 2 years, 0.81 (0.60 to 1.09); >2 to 5 years, 0.97 (0.77 to 1.22); and >5 years, 0.78 (0.64 to 0.96; Pinteraction=0.41). The absolute benefit was greatest in longest-duration HF; the number needed to treat for HF >5 years was 24 versus 32 for ≤6 months. CONCLUSIONS: Patients with longer-duration HF were older, had more comorbidities and symptoms, and had higher rates of worsening HF and death. The benefits of dapagliflozin were consistent across HF duration. Even patients with long-standing HF and generally mild symptoms are not stable, and it is not too late for such patients to benefit from a sodium-glucose cotransporter 2 inhibitor. REGISTRATION: URL: https://www. CLINICALTRIALS: gov; Unique identifier: NCT03619213.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Insuficiência Cardíaca Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Revista: Circulation Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Insuficiência Cardíaca Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Revista: Circulation Ano de publicação: 2023 Tipo de documento: Article