Heart attacks, or myocardial infarcts, are a major cause of death and disability in the UK. Immediate unblocking of the obstructed heart vessel with a balloon catheter and implantation of a mesh scaffold (stent) in heart centers is warranted in these patients. Morbidity and mortality in this patient group is related to the infarct size. Therefore, there is a need to discover novel therapeutic agents which reduce myocardial infarct size and preserve the contractile heart function. Large trials involving several thousand patients have demonstrated a survival benefit in patients with impaired heart function due to a heart attack, who received a mineralo-corticoid receptor antagonist (MRA, drug name: spironolactone). In these trials patients received the drug late, 3-14 days after the heart attack. Our proposal is to investigate whether MRA therapy administered intravenously prior to unblocking an occluded heart vessel, can reduce infarct size and as such can prevent long term sequelae of heart attacks. 150 patients admitted to 4 tertiary care hospitals (Heart Hospital London, London Chest, Essex Cardiothoracic Center and Leeds General Infirmary) for heart attack will be randomly assigned to receive MRA treatment or placebo. The first dose of the MRA will be applied intravenously immediately in the catheter suite, even before re-opening of the occluded vessel. From the second day on, patients will be prescribed oral MRA treatment, as a pill, for a total of three months. Before hospital discharge and after three months, a magnetic resonance image (MRI) of the heart will accurately investigate the evolution of infarct (scar) size and the contractile heart function and compare the group of patients who received the MRA drug versus the placebo control group. Of note, patients with an ejection fraction \<40% AND signs of heart failure OR diabetes will go on open label eplerenone according to current guidelines, instead of the study drug. This study will give first evidence, if very early MRA treatment improves heart function and should be used as early as possible for treatment of patients after a heart attack.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
61
Cardiothoracic Center - Basildon and Thurrock University Hospitals
Basildon, Essex, United Kingdom
London Chest Hospital
London, London, United Kingdom
Heart Hospital London
London, London, United Kingdom
Leeds Genereal Infirmary
Leeds, United Kingdom
Myocardial infarct (MI) size, as assessed by cardiac magnetic resonance imaging
Time frame: 12 weeks after STEMI
Markers of myocardial reperfusion injury
TIMI flow post-PPCI, ST-segment resolution post-PPCI
Time frame: 48 hours
Microvascular obstruction on cardiac MRI
hypodense area of late gadolinium enhancement
Time frame: 1-3 days after STEMI
Myocardial salvage
Area at risk assessed by T2 weighted imaging subtract final MI size
Time frame: 12 weeks
Acute myocardial infarct size
serum biomarkers: hsTnT, CK-MB, CK and cardiac MRI: late gadolinium enhancement
Time frame: 1-3 days
LV remodelling
LV end-diastolic and end-systolic volumes, LV ejection fraction, LV mass and wall-thickness
Time frame: 12 week cardiac MRI scan
Clinical outcome measures
cardiovascular death, non-fatal myocardial infarction, revascularisation, hospitalisation for heart failure, hyperkalemia, deterioration of kidney function, need for dialysis
Time frame: 12 weeks
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