Primary percutaneous coronary intervention (PPCI) is the preferred reperfusion strategy for treating acute ST-segment elevation myocardial infarction (STEMI). The main goals are to restore epicardial infarct-related artery patency and to achieve microvascular reperfusion as early as possible. No-reflow is the term used to describe inadequate myocardial perfusion of a given coronary segment without angiographic evidence of persistent mechanical obstruction of epicardial vessels and it refers to the high resistance of microvascular blood flow encountered during opening of the infarct-related coronary artery. Despite optimal evidence-based PPCI, myocardial no-reflow can still occur, negating many of the benefits of restoring culprit vessel patency, and is associated with a worse in-hospital and long-term prognosis. Several strategies have been tested to revert the no-reflow including the use of thrombectomy, glycoprotein IIb/IIIa inhibitors and the use of intracoronary adenosine, but none has been demonstrated to effectively counteract the phenomenon. The trial aims to show the effect of the administration of intracoronary adrenalin on myocardial reperfusion assessed by magnetic resonance in patients with STEMI undergoing PCI and with persistent coronary angiographic The Thrombolysis in Myocardial Infarction (TIMI) 0-1 flow during the interventional procedure after failure of standard therapy.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
NONE
after failure of standard therapy patients will treated with epinephrine
patients will receive standard therapy only
Division of Cardiology, Pulmonary Disease and Vascular Medicine
Düsseldorf, Germany
myocardial infarct size (% total LV mass)
cMRI parameters: myocardial infarct size (% total LV mass)
Time frame: 48-72 hours post intervention
Incidence and extent of microvascular obstruction
cMRI parameter
Time frame: 48-72 hours and 30 days post intervention
Myocardial salvage index (MSI)
cMRI parameter
Time frame: 48-72 hours and 30 days post intervention
Intra-myocardial haemorrhage (IMH)
cMRI parameter
Time frame: 48-72 hours and 30 days post intervention
LV ejection fraction (LVEF) and volumes
cMRI parameter
Time frame: 48-72 hours and 30 days post intervention
Thrombolysis in Myocardial Infarction (TIMI) flow grade)
Angiographic markers
Time frame: 48-72 hours post intervention
Myocardial blush grade (MBG)
Angiographic markers
Time frame: 48-72 hours post intervention
Computer-assisted myocardial blush quantification using the software 'Quantitative Blush Evaluator' (QuBE)
Angiographic markers
Time frame: 48-72 hours post intervention
Degree of ST segment resolution on ECG
Time frame: 48-72 hours post intervention
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