The RATIO Study is a multicenter, nationwide, randomized, controlled, single blinded, unfunded trial of n. 900 patients undergoing multivessel OPCAB (≥2 grafts). This study is designed to test in patients undergoing off-pump coronary artery bypass surgery the hypothesis that full (high dose, 300 U/kg) and half (low dose,150 U/kg) heparinization are not different in terms of thrombotic complications and major perioperative bleeding events (null hypothesis).
Off-pump coronary artery bypass grafting (OPCAB) is an established alternative to on-pump coronary artery bypass grafting (CABG). OPCAB determines a pro-coagulant state potentially deleterious on grafts patency, that is not counterbalanced by the adverse effects of cardiopulmonary bypass on coagulation occurring in CABG, and that lasts as long as one month. Therefore in OPCAB systemic heparinization is necessary to prevent thrombotic complications during transitory occlusion of coronary arteries and grafts. An internationally accepted standard intra-operative anticoagulation protocol for OPCAB has not yet been defined, and heparinization in OPCAB is a highly variable practice. The intraoperative anticoagulation regimen adopted in patients undergoing OPCAB may influence major postoperative outcomes, such as bleeding, transfusion requirements, inflammatory response, myocardial ischemia and grafts patency, but it has never been the object of large-scale randomized controlled trial (RCT). The 2 most widespread intraoperative anticoagulation protocols in OPCAB are represented by full (300 U/kg) or half (150 U/kg) heparinization, with target ACT ranging from 200 sec to \>480 sec. Patients enrolled in the study will be randomized to receive full or half heparinization in a 1:1 ratio using a randomization schedule blocked by site. Randomization will take place in the operatory room by the anesthesiologist, and will be blinded to the surgeon.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
900
Jilin Heart Hospital
Changchun, Jilin, China
RECRUITINGASST Lecco
Lecco, Italy
RECRUITINGAzienda Ospedaliera Universitaria di Sassari
Sassari, Italy
RECRUITINGComposite vascular
Death from vascular causes, perioperative myocardial infarction, stroke.
Time frame: 30 days post-operatively
Composite major bleeding
Redo for excessive bleeding, cardiac tamponade, transfusion ≥3 Units of packed red cells or of platelets.
Time frame: 48 hours post-operatively
Post-operative bleeding
Total bleeding evaluated the morning after surgery (ml.)
Time frame: 48 hours post-operatively
Transfusion of packed red cells (<3 Units) or of platelets
Time frame: 30 days post-operatively
Peak value of cardiac biomarker
Time frame: 30 days post-operatively
Transient ischemic cerebral attack
Time frame: 30 days post-operatively
Mesenteric ischemia (angiography or CT scan)
Time frame: 30 days post-operatively
Pulmonary embolus (angiography or CT scan)
Time frame: 30 days post-operatively
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.