The prevention of perioperative atrial fibrillation (AF) and myocardial injury after non-cardiac surgery (MINS) has the potential to reduce mortality, stroke, and hospital stays in patients undergoing major thoracic surgery. Data from cardiac surgery patients suggest that prevention of perioperative atrial fibrillation using an anti-inflammatory agent, such as colchicine, is feasible. The COP-AF trial will assess whether the administration of oral colchicine will reduce the incidence of perioperative atrial fibrillation and myocardial injury after non-cardiac surgery in patients undergoing major thoracic surgery.
Perioperative atrial fibrillation (AF) and myocardial injury after noncardiac surgery (MINS) are among the most common serious complications occurring after thoracic surgery. AF is the most common perioperative cardiac arrhythmia. The incidence of perioperative AF in patients undergoing major thoracic surgery ranges from 10% in low-risk patients to as high as 20% in high-risk patients. The course of patients with perioperative AF is frequently complicated by hemodynamic instability, problems with managing anticoagulation in the early postoperative period, prolonged intensive care unit and hospital stays, and increased costs. Patients who develop perioperative AF (POAF) or MINS also have a significantly increased risk of death and stroke. Colchicine is an inexpensive drug and a highly effective anti-inflammatory agent that holds great potential for preventing POAF and MINS in patients undergoing thoracic surgery. Data from cardiac surgery patients suggest that prevention of POAF using colchicine is feasible, but whether this concept is also applicable to patients undergoing thoracic surgery, where the risk of POAF is lower and underlying mechanisms may be different, is currently unclear. The 'Colchicine for the prevention of perioperative AF' (COP-AF) trial has been designed as a large randomized, double blind, placebo controlled trial to determine whether colchicine, a potent, safe and inexpensive anti-inflammatory drug, lowers the risk of perioperative AF, MINS, and other inflammatory complications in patients undergoing thoracic surgery. The primary objective of this trial is to determine whether a 10-day course of colchicine 0.5mg twice daily reduces the incidence of perioperative AF and MINS within 14 days after thoracic surgery.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Enrollment
3,209
Over-encapsulated 0.5mg tablet twice daily
Matching placebo capsule twice daily
Cleveland Clinic Florida
Weston, Florida, United States
Henry Ford Hospital
Detroit, Michigan, United States
Stony Brook University Hospital
Stony Brook, New York, United States
Wake Forest Baptist Medical Center
Winston-Salem, North Carolina, United States
Fairview Hospital
Cleveland, Ohio, United States
Clinically important perioperative atrial fibrillation/atrial flutter
Time frame: 14 days of randomization
Myocardial injury after noncardiac surgery
Time frame: 14 days of randomization
First occurrence of the composite of all-cause mortality, nonfatal myocardial injury after noncardiac surgery, or nonfatal stroke
Time frame: 14 days of randomization
First occurrence of the composite of all-cause mortality, nonfatal myocardial infarction, or nonfatal stroke
Time frame: 14 days of randomization
First occurrence of myocardial injury after noncardiac surgery not fulfilling the 4th universal definition of myocardial infarction
Time frame: 14 days of randomization
First occurrence of myocardial infarction
Time frame: 14 days of randomization
Time to chest tube removal
Time frame: 14 days of randomization
Duration of stay in ICU, step-down, and in-hospital
Time frame: 14 days of randomization
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The Ohio State University Wexner Medical Center
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