About this trial
Development of a new comprehensive method for perioperative prevention of atrial fibrillation paroxysms in cardiac surgery patients at the hospital stage.
It is planned to recruit 70 patients who will undergo pericardial fenestration during the operation using the original technique during coronary artery bypass grafting (Patent No. 2647626 C1 Russian Federation), and will be prescribed colchicine (the drug "Colchicum-dispert") in the perioperative period in order to prevent the development of paroxysms of atrial fibrillation in the postoperative period, and 70 cardiac surgery patients operated on using the standard technique (without performing the pericardial fenestration procedure intraoperatively), receiving non-steroidal anti-inflammatory drugs in the postoperative period.
Eligibility criteria
Qualifiers
Elective coronary artery bypass grafting on pump;
signed informed consent to participate in the study.
Disqualifiers
Reduced left ventricular ejection fraction (≤35%);
Valvular heart disease requiring surgical correction;
Liver failure with an increase in liver transaminases ≥1.5 times;
Renal failure (GFR<35 mL/min/1.73 m2 calculated with CKD-EPI);
Trial design
Treatments tested in this trial
- NSAID
- Colchicine 0.5 MG