TEERLINK, J. R., R. DIAZ, G. M. FELKER, J. J. V. MCMURRAY, M. METRA, S. D. SOLOMON, K. F. ADAMS, I. ANAND, A. ARIAS-MENDOZA, T. BIERING-SORENSEN, M. BOHM, D. BONDERMAN, J. G. F. CLELAND, R. CORBALAN, M. G. CRESPO-LEIRO, U. DAHLSTROM, L. E. ECHEVERRIA, J. M. C. FANG, G. FILIPPATOS, C. FONSECA, E. GONCALVESOVA, A. R. GOUDEV, J. G. HOWLETT, D. E.. LANFEAR, J. LI, M. LUND, P. MACDONALD, V. MAREEV, S. I. MOMOMURA, E. O MEARA, A. PARKHOMENKO, P. PONIKOWSKI, F. J. A. RAMIRES, P. SERPYTIS, K. SLIWA, Jindřich ŠPINAR, T. M. SUTER, J. TOMCSANYI, H. VANDEKERCKHOVE, D. VINEREANU, A. A. VOORS, M. B. YILMAZ, F. ZANNAD, L. SHARPSTEN, J. C. LEGG, C. VARIN, N. HONARPOUR, S. A. ABBASI, F. I. MALIK a C. E. KURTZ. Cardiac Myosin Activation with Omecamtiv Mecarbil in Systolic Heart Failure. New England Journal of Medicine. Waltham: Massachussetts Medical Society, 2021, roč. 384, č. 2, s. 105-116. ISSN 0028-4793. Dostupné z: https://dx.doi.org/10.1056/NEJMoa2025797.
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Základní údaje
Originální název Cardiac Myosin Activation with Omecamtiv Mecarbil in Systolic Heart Failure
Autoři TEERLINK, J. R. (garant), R. DIAZ, G. M. FELKER, J. J. V. MCMURRAY, M. METRA, S. D. SOLOMON, K. F. ADAMS, I. ANAND, A. ARIAS-MENDOZA, T. BIERING-SORENSEN, M. BOHM, D. BONDERMAN, J. G. F. CLELAND, R. CORBALAN, M. G. CRESPO-LEIRO, U. DAHLSTROM, L. E. ECHEVERRIA, J. M. C. FANG, G. FILIPPATOS, C. FONSECA, E. GONCALVESOVA, A. R. GOUDEV, J. G. HOWLETT, D. E.. LANFEAR, J. LI, M. LUND, P. MACDONALD, V. MAREEV, S. I. MOMOMURA, E. O MEARA, A. PARKHOMENKO, P. PONIKOWSKI, F. J. A. RAMIRES, P. SERPYTIS, K. SLIWA, Jindřich ŠPINAR (203 Česká republika, domácí), T. M. SUTER, J. TOMCSANYI, H. VANDEKERCKHOVE, D. VINEREANU, A. A. VOORS, M. B. YILMAZ, F. ZANNAD, L. SHARPSTEN, J. C. LEGG, C. VARIN, N. HONARPOUR, S. A. ABBASI, F. I. MALIK a C. E. KURTZ.
Vydání New England Journal of Medicine, Waltham, Massachussetts Medical Society, 2021, 0028-4793.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30218 General and internal medicine
Stát vydavatele Spojené státy
Utajení není předmětem státního či obchodního tajemství
WWW URL
Impakt faktor Impact factor: 176.079
Kód RIV RIV/00216224:14110/21:00121598
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.1056/NEJMoa2025797
UT WoS 000609886200010
Klíčová slova anglicky Cardiac Myosin Activation; Omecamtiv Mecarbil; Systolic Heart Failure
Štítky 14110115, rivok
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Mgr. Tereza Miškechová, učo 341652. Změněno: 17. 5. 2021 13:55.
Anotace
Among patients with heart failure and a reduced ejection fraction, those who received the cardiac myosin activator omecamtiv mecarbil had a lower incidence of a composite of heart-failure events or cardiovascular death at a median of 22 months than those who received placebo. Background The selective cardiac myosin activator omecamtiv mecarbil has been shown to improve cardiac function in patients with heart failure with a reduced ejection fraction. Its effect on cardiovascular outcomes is unknown. Methods We randomly assigned 8256 patients (inpatients and outpatients) with symptomatic chronic heart failure and an ejection fraction of 35% or less to receive omecamtiv mecarbil (using pharmacokinetic-guided doses of 25 mg, 37.5 mg, or 50 mg twice daily) or placebo, in addition to standard heart-failure therapy. The primary outcome was a composite of a first heart-failure event (hospitalization or urgent visit for heart failure) or death from cardiovascular causes. Results During a median of 21.8 months, a primary-outcome event occurred in 1523 of 4120 patients (37.0%) in the omecamtiv mecarbil group and in 1607 of 4112 patients (39.1%) in the placebo group (hazard ratio, 0.92; 95% confidence interval [CI], 0.86 to 0.99; P=0.03). A total of 808 patients (19.6%) and 798 patients (19.4%), respectively, died from cardiovascular causes (hazard ratio, 1.01; 95% CI, 0.92 to 1.11). There was no significant difference between groups in the change from baseline on the Kansas City Cardiomyopathy Questionnaire total symptom score. At week 24, the change from baseline for the median N-terminal pro-B-type natriuretic peptide level was 10% lower in the omecamtiv mecarbil group than in the placebo group; the median cardiac troponin I level was 4 ng per liter higher. The frequency of cardiac ischemic and ventricular arrhythmia events was similar in the two groups. Conclusions Among patients with heart failure and a reduced ejection, those who received omecamtiv mecarbil had a lower incidence of a composite of a heart-failure event or death from cardiovascular causes than those who received placebo. (Funded by Amgen and others; GALACTIC-HF ClinicalTrials.gov number, ; EudraCT number, 2016-002299-28.)
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