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Levosimendan Improves Hemodynamics and Exercise Tolerance in PH-HFpEF: Results of the Randomized Placebo-Controlled HELP Trial.
Burkhoff, Daniel; Borlaug, Barry A; Shah, Sanjiv J; Zolty, Ronald; Tedford, Ryan J; Thenappan, Thenappan; Zamanian, Roham T; Mazurek, Jeremy A; Rich, Jonathan D; Simon, Marc A; Chung, Eugene S; Raza, Farhan; Majure, David T; Lewis, Gregory D; Preston, Ioana R; Rich, Stuart.
Afiliação
  • Burkhoff D; Cardiovascular Research Foundation, New York, New York, USA. Electronic address: dburkhoff@crf.org.
  • Borlaug BA; Mayo Clinic, Rochester, Minnesota.
  • Shah SJ; Northwestern University, Chicago, Illinois, USA.
  • Zolty R; University of Nebraska Medical Center, Omaha, Nebraska, USA.
  • Tedford RJ; Medical University of South Carolina, Charleston, South Carolina, USA.
  • Thenappan T; University of Minnesota, Minneapolis, Minnesota, USA.
  • Zamanian RT; Stanford University, Stanford, California, USA.
  • Mazurek JA; Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Rich JD; Northwestern University, Chicago, Illinois, USA.
  • Simon MA; University of Pittsburgh, Pittsburgh, Pennsylvani, USA.
  • Chung ES; Lindner Research Center at The Christ Hospital, Cincinnati, Ohio, USA.
  • Raza F; University of Wisconsin, Madison, Wisconsin, USA.
  • Majure DT; North Shore University Hospital, Manhasset, New York, USA.
  • Lewis GD; Massachusetts, General Hospital, Boston, Massachusetts, USA.
  • Preston IR; Tufts Medical Center, Boston, Massachusetts, USA.
  • Rich S; Northwestern University, Chicago, Illinois, USA.
JACC Heart Fail ; 9(5): 360-370, 2021 05.
Article em En | MEDLINE | ID: mdl-33839076
OBJECTIVES: The purpose of this study was to evaluate the effects of intravenous levosimendan on hemodynamics and 6-min walk distance (6MWD) in patients with pulmonary hypertension and heart failure with preserved ejection fraction (PH-HFpEF). BACKGROUND: There are no proven effective treatments for patients with PH-HFpEF. METHODS: Patients with mean pulmonary artery pressure (mPAP) ≥35 mm Hg, pulmonary capillary wedge pressure (PCWP) ≥20 mm Hg, and LVEF ≥40% underwent 6MWD and hemodynamic measurements at rest, during passive leg raise, and supine cycle exercise at baseline and after an open-label 24-h levosimendan infusion (0.1 µg/kg/min). Hemodynamic responders (those with ≥4 mm Hg reduction of exercise-PCWP) were randomized (double blind) to weekly levosimendan infusion (0.075 to 0.1 ug/kg/min for 24 h) or placebo for 5 additional weeks. The primary end point was exercise-PCWP, and key secondary end points included 6MWD and PCWP measured across all exercise stages. RESULTS: Thirty-seven of 44 patients (84%) met responder criteria and were randomized to levosimendan (n = 18) or placebo (n = 19). Participants were 69 ± 9 years of age, 61% female, and with resting mPAP 41.0 ± 9.3 mm Hg and exercise-PCWP 36.8 ± 11.3 mm Hg. Compared with placebo, levosimendan did not significantly reduce the primary end point of exercise-PCWP at 6 weeks (-1.4 mm Hg; 95% confidence interval [CI]: -7.8 to 4.8; p = 0.65). However, levosimendan reduced PCWP measured across all exercise stages (-3.9 ± 2.0 mm Hg; p = 0.047). Levosimendan treatment resulted in a 29.3 m (95% CI: 2.5 to 56.1; p = 0.033) improvement in 6MWD compared with placebo. CONCLUSIONS: Six weeks of once-weekly levosimendan infusion did not affect exercise-PCWP but did reduce PCWP incorporating data from rest and exercise, in tandem with increased 6MWD. Further study of levosimendan is warranted as a therapeutic option for PH-HFpEF. (Hemodynamic Evaluation of Levosimendan in Patients With PH-HFpEF [HELP]; NCT03541603).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tolerância ao Exercício / Insuficiência Cardíaca Tipo de estudo: Clinical_trials Limite: Female / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tolerância ao Exercício / Insuficiência Cardíaca Tipo de estudo: Clinical_trials Limite: Female / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article