TEERLINK, JR, R DIAZ, GM FELKER, JJV MCMURRAY, M METRA, SD SOLOMON, KF ADAMS, I ANAND, A ARIAS-MENDOZA, T BIERING-SORENSEN, M BOHM, D BONDERMAN, JGF CLELAND, R CORBALAN, MG CRESPO-LEIRO, U DAHLSTROM, LEE CORREA, JMC FANG, G FILIPPATOS, C FONSECA, E GONCALVESOVA, AR GOUDEV, JG HOWLETT, DE LANFEAR, M LUND, P MACDONALD, V MAREEV, SI MOMOMURA, O Meara E, A PARKHOMENKO, P PONIKOWSKI, FJA RAMIRES, P SERPYTIS, K SLIWA, Jindřich ŠPINAR, TM SUTER, J TOMCSANYI, H VANDEKERCKHOVE, D VINEREANU, AA VOORS, MB YILMAZ, F ZANNAD, L SHARPSTEN, JC LEGG, SA ABBASI, C VARIN, FI MALIK a CE KURTZ. Omecamtiv mecarbil in chronic heart failure with reduced ejection fraction: GALACTIC-HF baseline characteristics and comparison with contemporary clinical trials. European Journal of heart Failure. Hoboken: Wiley, 2020, roč. 22, č. 11, s. 2160-2171. ISSN 1388-9842. Dostupné z: https://dx.doi.org/10.1002/ejhf.2015.
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Základní údaje
Originální název Omecamtiv mecarbil in chronic heart failure with reduced ejection fraction: GALACTIC-HF baseline characteristics and comparison with contemporary clinical trials
Autoři TEERLINK, JR, R DIAZ, GM FELKER, JJV MCMURRAY, M METRA, SD SOLOMON, KF ADAMS, I ANAND, A ARIAS-MENDOZA, T BIERING-SORENSEN, M BOHM, D BONDERMAN, JGF CLELAND, R CORBALAN, MG CRESPO-LEIRO, U DAHLSTROM, LEE CORREA, JMC FANG, G FILIPPATOS, C FONSECA, E GONCALVESOVA, AR GOUDEV, JG HOWLETT, DE LANFEAR, M LUND, P MACDONALD, V MAREEV, SI MOMOMURA, O Meara E, A PARKHOMENKO, P PONIKOWSKI, FJA RAMIRES, P SERPYTIS, K SLIWA, Jindřich ŠPINAR, TM SUTER, J TOMCSANYI, H VANDEKERCKHOVE, D VINEREANU, AA VOORS, MB YILMAZ, F ZANNAD, L SHARPSTEN, JC LEGG, SA ABBASI, C VARIN, FI MALIK a CE KURTZ.
Vydání European Journal of heart Failure, Hoboken, Wiley, 2020, 1388-9842.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Stát vydavatele Spojené státy
Utajení není předmětem státního či obchodního tajemství
WWW URL
Impakt faktor Impact factor: 15.534
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.1002/ejhf.2015
UT WoS 000583618200001
Klíčová slova anglicky Heart failure; Omecamtiv mecarbil; Cardiac myosin activator; Inotrope; Myotrope; Cardiovascular outcomes trial
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Mgr. Tereza Miškechová, učo 341652. Změněno: 9. 12. 2020 10:55.
Anotace
Aims The safety and efficacy of the novel selective cardiac myosin activator, omecamtiv mecarbil, in patients with heart failure with reduced ejection fraction (HFrEF) is being tested in the Global Approach to Lowering Adverse Cardiac outcomes Through Improving Contractility in Heart Failure (GALACTIC-HF) trial. Here we describe the baseline characteristics of participants in GALACTIC-HF and how these compare with other contemporary trials. Methods and results Adults with established HFrEF, New York Heart Association (NYHA) functional class >= II, ejection fraction <= 35%, elevated natriuretic peptides and either current hospitalization for heart failure or history of hospitalization/emergency department visit for heart failure within a year were randomized to either placebo or omecamtiv mecarbil (pharmacokinetic-guided dosing: 25, 37.5, or 50 mg bid). A total of 8256 patients [male (79%), non-white (22%), mean age 65 years] were enrolled with a mean ejection fraction 27%, ischaemic aetiology in 54%, NYHA class II 53% and III/IV 47%, and median N-terminal pro-B-type natriuretic peptide 1971 pg/mL. Heart failure therapies at baseline were among the most effectively employed in contemporary heart failure trials. GALACTIC-HF randomized patients representative of recent heart failure registries and trials with substantial numbers of patients also having characteristics understudied in previous trials including more from North America (n = 1386), enrolled as inpatients (n = 2084), systolic blood pressure <100 mmHg (n = 1127), estimated glomerular filtration rate <30 mL/min/1.73 m(2) (n = 528), and treated with sacubitril/valsartan at baseline (n = 1594). Conclusions GALACTIC-HF enrolled a well-treated, high-risk population from both inpatient and outpatient settings, which will provide a definitive evaluation of the efficacy and safety of this novel therapy, as well as informing its potential future implementation.
VytisknoutZobrazeno: 9. 10. 2024 19:02