The study will include patients with acute coronary syndrome without ST segment elevation and multivessel CA lesion, who are subject to surgical treatment according to KG data (Syntax Score 23 - 32 points with significant damage to the anterior descending artery and/or trunk of the left coronary artery). The patient should be suitable for both CABG and PCI (confirmed by an X-ray surgeon and a cardiac surgeon). An X-ray surgeon and a cardiac surgeon, within the framework of planning the volume of revascularization, strives for the fullest feasible volume. Complete myocardial revascularization (that is, the desire for the absence of hemodynamically significant coronary arteries after revascularization, with a diameter of \> 2.5 mm, that is, residual coronary artery stenosis of no more than 60%). Thus, patients will be randomized into groups in a ratio of 1:1. Each group will need to include 230 patients (a total of 460). In the main group, revascularization will be performed by PCI, in the control group by CABG.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
460
revascularization
Anton
Novosibirsk, Novosibirsk Obl, Russia
RECRUITINGAnton
Novosibirsk, Rechkunovskaya Str., Russia
RECRUITINGDeath from any cause
a fatal outcome due to any cause or disease
Time frame: 1 year
Combined endpoint (death from cardiovascular causes, MI, Stroke, repeated unplanned myocardial revascularization)
Death from cardiovascular causes, MI, Stroke, repeated unplanned myocardial revascularization.
Time frame: 1 year
target LDL level
Achieved target LDL level
Time frame: 1 year
Myocardial infarction
Myocardial infarction (Fourth universal definition of myocardial infarction (2018))
Time frame: 1 year
Stroke
clinically verified acute cerebrovascular accident of any etiology (hemorrhagic or ischemic)
Time frame: 1 year
Repeated unplanned myocardial revascularization
any type of repeated myocardial revascularization by endovascular or cardiac surgery performed in the time period after index revascularization;
Time frame: 1 year
Duration of the hospital period
the number of bed days that the patient spent in the clinic in connection with an index event and/or complications arising from the underlying, concomitant diseases, as well as in connection with the treatment.
Time frame: 1 year
Intra/perioperative complications
Any intra/perioperative complications (MI, Stroke, hemorrhagic complication, )
Time frame: 1 year
Significant hemorrhagic complications (grade 3 or more on the BARC scale)
any bleeding that occurred during or after the index revascularization of the myocardium, leading to a clinically significant decrease in hemoglobin levels, requiring hemotransfusion and/or surgical methods of hemostasis, artery dissection, shunt thrombosis, and other
Time frame: 1 year
Questionnaire
SF-36 Quality of Life Questionnaire and Rose Questionn
Time frame: 1 year
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