LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 3 of total 3

Search options

  1. Article ; Online: Efficacy of omecamtiv mecarbil in heart failure with reduced ejection fraction according to N-terminal pro-B-type natriuretic peptide level: insights from the GALACTIC-HF trial.

    Docherty, Kieran F / McMurray, John J V / Claggett, Brian L / Miao, Zi Michael / Adams, Kirkwood F / Arias-Mendoza, Alexandra / Cleland, John G F / Diaz, Rafael / Echeverria Correa, Luis E / Felker, G Michael / Fonseca, Candida / Li, Jing / Metra, Marco / Sliwa-Hahnle, Karen / Solomon, Scott D / Vandekerckhove, Hans J / Vinereanu, Dragos / Voors, Adriaan A / Heitner, Stephen B /
    Kupfer, Stuart / Malik, Fady I / Meng, Lisa / Teerlink, John R

    European journal of heart failure

    2023  Volume 25, Issue 2, Page(s) 248–259

    Abstract: Aim: N-terminal pro-B-type natriuretic peptide (NT-proBNP) is predictive of both outcomes and response to treatment in patients with heart failure with reduced ejection fraction (HFrEF). The aim of this study was to examine the effect of the cardiac ... ...

    Abstract Aim: N-terminal pro-B-type natriuretic peptide (NT-proBNP) is predictive of both outcomes and response to treatment in patients with heart failure with reduced ejection fraction (HFrEF). The aim of this study was to examine the effect of the cardiac myosin activator omecamtiv mecarbil according to baseline NT-proBNP level in the Global Approach to Lowering Adverse Cardiac outcomes Through Improving Contractility in Heart Failure trial (GALACTIC-HF).
    Methods and results: The primary outcome was the composite of a worsening heart failure event (urgent clinic visit, emergency department visit, or hospitalization) or cardiovascular death. We prespecified analysis of the effect of treatment according to baseline NT-proBNP (≤ median, > median), excluding individuals with atrial fibrillation/flutter (AF/AFL). Of the 8232 patients analysed, 8206 had an available baseline NT-proBNP measurement. Among the 5971 patients not in AF/AFL, the median (Q1-Q3) NT-proBNP level was 1675 (812-3579) pg/ml. Hazard ratios (HR) for the effect of omecamtiv mecarbil, compared with placebo, for the primary endpoint in patients without AF/AFL were: ≤ median 0.94 (95% confidence interval [CI] 0.80-1.09), > median 0.81 (0.73-0.90) (p-interaction = 0.095); for the overall population (including patients with AF/AFL) the HRs were ≤ median 1.01 (0.90-1.15) and > median 0.88 (0.80-0.96) (p-interaction = 0.035). There was an interaction between treatment and NT-proBNP, examined as a continuous variable, with greater effect of omecamtiv mecarbil on the primary outcome in patients with a higher baseline NT-proBNP (p-interaction = 0.086).
    Conclusions: In GALACTIC-HF, the benefit of omecamtiv mecarbil appeared to be larger in patients with higher baseline NT-proBNP levels, especially in patients without AF/AFL.
    Clinical trial registration: ClinicalTrials.gov Identifier NCT02929329; EudraCT number, 2016-002299-28.
    MeSH term(s) Humans ; Atrial Fibrillation ; Biomarkers ; Heart Failure ; Natriuretic Peptide, Brain/therapeutic use ; Peptide Fragments/therapeutic use ; Prognosis ; Stroke Volume/physiology
    Chemical Substances Biomarkers ; Natriuretic Peptide, Brain (114471-18-0) ; omecamtiv mecarbil (2M19539ERK) ; Peptide Fragments ; pro-brain natriuretic peptide (1-76)
    Language English
    Publishing date 2023-01-16
    Publishing country England
    Document type Journal Article ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ZDB-ID 1483672-5
    ISSN 1879-0844 ; 1388-9842
    ISSN (online) 1879-0844
    ISSN 1388-9842
    DOI 10.1002/ejhf.2763
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article ; Online: Omecamtiv mecarbil in chronic heart failure with reduced ejection fraction: GALACTIC-HF baseline characteristics and comparison with contemporary clinical trials.

    Teerlink, John R / Diaz, Rafael / Felker, G Michael / McMurray, John J V / Metra, Marco / Solomon, Scott D / Adams, Kirkwood F / Anand, Inder / Arias-Mendoza, Alexandra / Biering-Sørensen, Tor / Böhm, Michael / Bonderman, Diana / Cleland, John G F / Corbalan, Ramon / Crespo-Leiro, Maria G / Dahlström, Ulf / Echeverria Correa, Luis E / Fang, James C / Filippatos, Gerasimos /
    Fonseca, Cândida / Goncalvesova, Eva / Goudev, Assen R / Howlett, Jonathan G / Lanfear, David E / Lund, Mayanna / Macdonald, Peter / Mareev, Vyacheslav / Momomura, Shin-Ichi / O'Meara, Eileen / Parkhomenko, Alexander / Ponikowski, Piotr / Ramires, Felix J A / Serpytis, Pranas / Sliwa, Karen / Spinar, Jindrich / Suter, Thomas M / Tomcsanyi, Janos / Vandekerckhove, Hans / Vinereanu, Dragos / Voors, Adriaan A / Yilmaz, Mehmet B / Zannad, Faiez / Sharpsten, Lucie / Legg, Jason C / Abbasi, Siddique A / Varin, Claire / Malik, Fady I / Kurtz, Christopher E

    European journal of heart failure

    2020  Volume 22, Issue 11, Page(s) 2160–2171

    Abstract: 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 ... ...

    Abstract 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
    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.
    MeSH term(s) Aged ; Female ; Heart Failure/drug therapy ; Heart Failure/physiopathology ; Humans ; Male ; Middle Aged ; Randomized Controlled Trials as Topic ; Stroke Volume/drug effects ; Urea/analogs & derivatives ; Urea/therapeutic use ; Ventricular Function, Left/drug effects
    Chemical Substances omecamtiv mecarbil (2M19539ERK) ; Urea (8W8T17847W)
    Language English
    Publishing date 2020-10-27
    Publishing country England
    Document type Journal Article ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ZDB-ID 1483672-5
    ISSN 1879-0844 ; 1388-9842
    ISSN (online) 1879-0844
    ISSN 1388-9842
    DOI 10.1002/ejhf.2015
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  3. Article ; Online: Baseline Characteristics of Patients With Heart Failure and Preserved Ejection Fraction in the PARAGON-HF Trial.

    Solomon, Scott D / Rizkala, Adel R / Lefkowitz, Martin P / Shi, Victor C / Gong, JianJian / Anavekar, Nagesh / Anker, Stefan D / Arango, Juan L / Arenas, Jose L / Atar, Dan / Ben-Gal, Turia / Boytsov, Sergey A / Chen, Chen-Huan / Chopra, Vijay K / Cleland, John / Comin-Colet, Josep / Duengen, Hans-Dirk / Echeverría Correa, Luis E / Filippatos, Gerasimos /
    Flammer, Andreas J / Galinier, Michel / Godoy, Armando / Goncalvesova, Eva / Janssens, Stefan / Katova, Tzvetana / Køber, Lars / Lelonek, Małgorzata / Linssen, Gerard / Lund, Lars H / O'Meara, Eileen / Merkely, Béla / Milicic, Davor / Oh, Byung-Hee / Perrone, Sergio V / Ranjith, Naresh / Saito, Yoshihiko / Saraiva, Jose F / Shah, Sanjiv / Seferovic, Petar M / Senni, Michele / Sibulo, Antonio S / Sim, David / Sweitzer, Nancy K / Taurio, Jyrki / Vinereanu, Dragos / Vrtovec, Bojan / Widimský, Jiří / Yilmaz, Mehmet B / Zhou, Jingmin / Zweiker, Robert / Anand, Inder S / Ge, Junbo / Lam, Carolyn S P / Maggioni, Aldo P / Martinez, Felipe / Packer, Milton / Pfeffer, Marc A / Pieske, Burkert / Redfield, Margaret M / Rouleau, Jean L / Van Veldhuisen, Dirk J / Zannad, Faiez / Zile, Michael R / McMurray, John J V

    Circulation. Heart failure

    2018  Volume 11, Issue 7, Page(s) e004962

    Abstract: Background: To describe the baseline characteristics of patients with heart failure and preserved left ventricular ejection fraction enrolled in the PARAGON-HF trial (Prospective Comparison of Angiotensin Receptor Neprilysin Inhibitor With Angiotensin ... ...

    Abstract Background: To describe the baseline characteristics of patients with heart failure and preserved left ventricular ejection fraction enrolled in the PARAGON-HF trial (Prospective Comparison of Angiotensin Receptor Neprilysin Inhibitor With Angiotensin Receptor Blocker Global Outcomes in HFpEF) comparing sacubitril/valsartan to valsartan in reducing morbidity and mortality.
    Methods and results: We report key demographic, clinical, and laboratory findings, and baseline therapies, of 4822 patients randomized in PARAGON-HF, grouped by factors that influence criteria for study inclusion. We further compared baseline characteristics of patients enrolled in PARAGON-HF with those patients enrolled in other recent trials of heart failure with preserved ejection fraction (HFpEF). Among patients enrolled from various regions (16% Asia-Pacific, 37% Central Europe, 7% Latin America, 12% North America, 28% Western Europe), the mean age of patients enrolled in PARAGON-HF was 72.7±8.4 years, 52% of patients were female, and mean left ventricular ejection fraction was 57.5%, similar to other trials of HFpEF. Most patients were in New York Heart Association class II, and 38% had ≥1 hospitalizations for heart failure within the previous 9 months. Diabetes mellitus (43%) and chronic kidney disease (47%) were more prevalent than in previous trials of HFpEF. Many patients were prescribed angiotensin-converting enzyme inhibitors or angiotensin receptor blockers (85%), β-blockers (80%), calcium channel blockers (36%), and mineralocorticoid receptor antagonists (24%). As specified in the protocol, virtually all patients were on diuretics, had elevated plasma concentrations of N-terminal pro-B-type natriuretic peptide (median, 911 pg/mL; interquartile range, 464-1610), and structural heart disease.
    Conclusions: PARAGON-HF represents a contemporary group of patients with HFpEF with similar age and sex distribution compared with prior HFpEF trials but higher prevalence of comorbidities. These findings provide insights into the impact of inclusion criteria on, and regional variation in, HFpEF patient characteristics.
    Clinical trial registration: URL: https://www.clinicaltrials.gov. Unique identifier: NCT01920711.
    MeSH term(s) Adrenergic beta-Antagonists/therapeutic use ; Aged ; Aged, 80 and over ; Angiotensin II Type 1 Receptor Blockers/therapeutic use ; Angiotensin Receptor Antagonists/therapeutic use ; Angiotensin-Converting Enzyme Inhibitors/therapeutic use ; Clinical Trials as Topic ; Female ; Heart Failure/drug therapy ; Heart Failure/physiopathology ; Humans ; Male ; Middle Aged ; Mineralocorticoid Receptor Antagonists/therapeutic use ; Stroke Volume/drug effects ; Valsartan/therapeutic use ; Ventricular Function, Left/drug effects
    Chemical Substances Adrenergic beta-Antagonists ; Angiotensin II Type 1 Receptor Blockers ; Angiotensin Receptor Antagonists ; Angiotensin-Converting Enzyme Inhibitors ; Mineralocorticoid Receptor Antagonists ; Valsartan (80M03YXJ7I)
    Language English
    Publishing date 2018-07-02
    Publishing country United States
    Document type Journal Article ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ZDB-ID 2429459-7
    ISSN 1941-3297 ; 1941-3289
    ISSN (online) 1941-3297
    ISSN 1941-3289
    DOI 10.1161/CIRCHEARTFAILURE.118.004962
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

To top