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Baseline characteristics of patients with heart failure with mildly reduced or preserved ejection fraction: The FINEARTS-HF trial.
Solomon, Scott D; Ostrominski, John W; Vaduganathan, Muthiah; Claggett, Brian; Jhund, Pardeep S; Desai, Akshay S; Lam, Carolyn S P; Pitt, Bertram; Senni, Michele; Shah, Sanjiv J; Voors, Adriaan A; Zannad, Faiez; Abidin, Imran Zainal; Alcocer-Gamba, Marco Antonio; Atherton, John J; Bauersachs, Johann; Ma, Chang-Sheng; Chiang, Chern-En; Chioncel, Ovidiu; Chopra, Vijay; Comin-Colet, Josep; Filippatos, Gerasimos; Fonseca, Cândida; Gajos, Grzegorz; Goland, Sorel; Goncalvesová, Eva; Kang, Seok-Min; Katova, Tzvetana; Kosiborod, Mikhail N; Latkovskis, Gustavs; Lee, Alex Pui-Wai; Linssen, Gerard C M; Llamas-Esperón, Guillermo; Mareev, Vyacheslav; Martinez, Felipe A; Melenovský, Vojtech; Merkely, Béla; Nodari, Savina; Petrie, Mark C; Saldarriaga, Clara Inés; Saraiva, Jose Francisco Kerr; Sato, Naoki; Schou, Morten; Sharma, Kavita; Troughton, Richard; Udell, Jacob A; Ukkonen, Heikki; Vardeny, Orly; Verma, Subodh; von Lewinski, Dirk.
Afiliação
  • Solomon SD; Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • Ostrominski JW; Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • Vaduganathan M; Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • Claggett B; Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • Jhund PS; BHF Glasgow Cardiovascular Research Center, School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, UK.
  • Desai AS; 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.
  • Pitt B; University of Michigan, School of Medicine, Ann Arbor, MI, USA.
  • Senni M; University Bicocca Milan, Italy, and, Papa Giovanni XXIII Hospital, Bergamo, Italy.
  • Shah SJ; Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Voors AA; University Medical Center Groningen, Groningen, The Netherlands.
  • Zannad F; Université de Lorraine, Inserm Clinical Investigation Centre, CHU, Nancy, France.
  • Abidin IZ; University of Malaya, Kuala Lumpur, Malaysia.
  • Alcocer-Gamba MA; Centro de Estudios Clínicos de Querétaro, Querétaro, Mexico.
  • Atherton JJ; Cardiology Research Department, Royal Brisbane and Women's Hospital, University of Queensland, Brisbane, QLD, Australia.
  • Bauersachs J; Department of Cardiology and Angiology, Hannover Medical School, Hannover, Germany.
  • Ma CS; Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
  • Chiang CE; Taipei Veterans General Hospital, Taipei, Taiwan.
  • Chioncel O; Emergency Institute for Cardiovascular Diseases 'Prof. Dr. C.C. Iliescu', University of Medicine Carol Davila, Bucharest, Romania.
  • Chopra V; Clinical Cardiology, Heart Failure and Research, Max Super Specialty Hospital, New Delhi, India.
  • Comin-Colet J; Department of Cardiology, Bellvitge University Hospital and Bellvitge Biomedical Research Institute, CIBER-CV, University of Barcelona, L'Hospitalet de Llobregat, Barcelona, Spain.
  • Filippatos G; Department of Cardiology, Attikon University Hospital, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.
  • Fonseca C; Department of Internal Medicine, Hospital São Francisco Xavier, NOVA Medical School, Universidade Nova de Lisboa, Lisbon, Portugal.
  • Gajos G; Department of Coronary Disease and Heart Failure, Jagiellonian University Medical College, Kraków, Poland.
  • Goland S; Heart Failure Unit, Kaplan Medical Center, Rehovot, Israel.
  • Goncalvesová E; Faculty of Medicine, Comenius University, Bratislava, Slovakia.
  • Kang SM; Division of Cardiology, Severance Hospital, Yonsei University Health System, Seoul, South Korea.
  • Katova T; Department of Noninvasive Cardiology, National Cardiology Hospital, Sofia, Bulgaria.
  • Kosiborod MN; Saint Luke's Mid America Heart Institute, University of Missouri-Kansas City, Kansas City, MO, USA.
  • Latkovskis G; Latvian Center of Cardiology, Pauls Stradins Clinical University Hospital, Riga, Latvia.
  • Lee AP; Li Ka Shing Institute of Health Sciences, The Chinese University of Hong Kong, Hong Kong, China.
  • Linssen GCM; Department of Cardiology, Hospital Group Twente, Almelo, The Netherlands.
  • Llamas-Esperón G; Hospital Cardiologico Aguascalientes, Aguascalientes, Mexico.
  • Mareev V; University Clinic of Lomonosov Moscow State University, Moscow, Russia.
  • Martinez FA; Universidad Nacional de Córdoba, Córdoba, Argentina.
  • Melenovský V; Department of Cardiology, Institute for Clinical and Experimental Medicine (IKEM), Prague, Czech Republic.
  • Merkely B; Heart and Vascular Center, Semmelweis University, Budapest, Hungary.
  • Nodari S; Department of Cardiology, University of Brescia and ASST 'Spedali Civili' Hospital, Brescia, Italy.
  • Petrie MC; BHF Glasgow Cardiovascular Research Center, School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, UK.
  • Saldarriaga CI; Centro Cardiovascular Colombiano, Clínica Santa María, Antioquia, Colombia.
  • Saraiva JFK; Cardiovascular Division, Instituto de Pesquisa Clínica de Campinas, Campinas, Brazil.
  • Sato N; Kawaguchi Cardiovascular and Respiratory Hospital, Saitama, Japan.
  • Schou M; Department of Cardiology, Herlev-Gentofte University Hospital, Hellerup, Denmark.
  • Sharma K; Division of Cardiology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Troughton R; Christchurch Heart Institute, Department of Medicine, University of Otago, Christchurch, New Zealand.
  • Udell JA; Women's College Hospital and Peter Munk Cardiac Centre, Toronto General Hospital, University of Toronto, Toronto, ON, Canada.
  • Ukkonen H; Heart Centre, Turku University Hospital, Turku, Finland.
  • Vardeny O; Department of Medicine, University of Minnesota, Minneapolis VA Health Care System, Minneapolis, MN, USA.
  • Verma S; Division of Cardiac Surgery, St. Michael's Hospital, University of Toronto, Toronto, ON, Canada.
  • von Lewinski D; Division of Cardiology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Eur J Heart Fail ; 26(6): 1334-1346, 2024 Jun.
Article em En | MEDLINE | ID: mdl-38733212
ABSTRACT

AIMS:

To describe the baseline characteristics of participants in the FINEARTS-HF trial, contextualized with prior trials including patients with heart failure (HF) with mildly reduced and preserved ejection fraction (HFmrEF/HFpEF). The FINEARTS-HF trial is comparing the effects of the non-steroidal mineralocorticoid receptor antagonist finerenone with placebo in reducing cardiovascular death and total worsening HF events in patients with HFmrEF/HFpEF. METHODS AND

RESULTS:

Patients with symptomatic HF, left ventricular ejection fraction (LVEF) ≥40%, estimated glomerular filtration rate ≥ 25 ml/min/1.73 m2, elevated natriuretic peptide levels and evidence of structural heart disease were enrolled and randomized to finerenone titrated to a maximum of 40 mg once daily or matching placebo. We validly randomized 6001 patients to finerenone or placebo (mean age 72 ± 10 years, 46% women). The majority were New York Heart Association functional class II (69%). The baseline mean LVEF was 53 ± 8% (range 34-84%); 36% of participants had a LVEF <50% and 64% had a LVEF ≥50%. The median N-terminal pro-B-type natriuretic peptide (NT-proBNP) was 1041 (interquartile range 449-1946) pg/ml. A total of 1219 (20%) patients were enrolled during or within 7 days of a worsening HF event, and 3247 (54%) patients were enrolled within 3 months of a worsening HF event. Compared with prior large-scale HFmrEF/HFpEF trials, FINEARTS-HF participants were more likely to have recent (within 6 months) HF hospitalization and greater symptoms and functional limitations. Further, concomitant medications included a larger percentage of sodium-glucose cotransporter 2 inhibitors and angiotensin receptor-neprilysin inhibitors than previous trials.

CONCLUSIONS:

FINEARTS-HF has enrolled a broad range of high-risk patients with HFmrEF and HFpEF. The trial will determine the safety and efficacy of finerenone in this population.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Volume Sistólico / Antagonistas de Receptores de Mineralocorticoides / Insuficiência Cardíaca / Naftiridinas Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Volume Sistólico / Antagonistas de Receptores de Mineralocorticoides / Insuficiência Cardíaca / Naftiridinas Idioma: En Ano de publicação: 2024 Tipo de documento: Article