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Published on: September 15, 2023
The low-dose colchicine in patients after non-CABG cardiac surgery: a randomized controlled trial
Tuo Pan1,2, Chen-Yu Jiang3, He Zhang1
1Department of Cardio-Thoracic Surgery, Nanjing Drum Tower Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Graduate School of Peking Union Medical College, Number 321 Zhongshan Road, Nanjing, 210008, Jiangsu, China.
Insights
Low-dose colchicine effectively reduced myocardial injury and inflammation biomarkers after non-coronary artery bypass grafting (non-CABG) surgery. This treatment also decreased post-pericardiotomy syndrome, showing its benefit in cardiac surgery patients.
Area of Science:
- Cardiology
- Pharmacology
- Surgical Innovation
Background:
- Colchicine's anti-inflammatory properties are known to reduce cardiovascular events in post-myocardial infarction and chronic coronary disease patients.
- Its efficacy in myocardial protection during non-coronary artery bypass grafting (non-CABG) with cardiopulmonary bypass remains under investigation.
Purpose of the Study:
- To evaluate the cardioprotective effects of colchicine in patients undergoing non-CABG cardiac surgery.
- To assess the impact of perioperative colchicine on myocardial injury biomarkers and inflammatory markers.
Main Methods:
- A randomized, placebo-controlled trial involving 132 patients undergoing non-CABG cardiac surgery.
- Participants received either colchicine (0.5 mg daily) or placebo starting 72 hours pre-surgery for 5 days.
- Primary outcome: cardiac troponin T (cTnT) levels at 48 hours post-surgery; secondary outcomes included other biomarkers and adverse events.
Main Results:
- Colchicine significantly reduced postoperative levels of cTnT, cardiac troponin I (cTnI), creatine kinase-MB (CK-MB), and interleukin-6 compared to placebo.
- The colchicine group showed a significant decrease in post-pericardiotomy syndrome (3.08% vs. 17.7%).
- An increased rate of diarrhea was noted in the colchicine group (9.23% vs. 0%), with no significant differences in other adverse events.
Conclusions:
- Perioperative low-dose colchicine effectively attenuates myocardial injury and inflammation biomarkers post-non-CABG cardiac surgery.
- Colchicine significantly reduced the incidence of post-pericardiotomy syndrome.
- The findings support colchicine's role in improving outcomes for patients undergoing non-CABG cardiac surgery.
Background:
Recent high-quality trials have shown that the anti-inflammatory effects of colchicine reduce the risk of cardiovascular events in patients suffering post-myocardial infarction and chronic coronary disease. The effect of colchicine in patients undergoing non-coronary artery bypass grafting (non-CABG) with cardiopulmonary bypass remains unclear. We aim to evaluate the effect of colchicine on myocardial protection in patients who underwent non-CABG cardiac surgery.
Method:
Patients were randomly assigned to colchicine or placebo groups starting 72 h before scheduled cardiac surgery and for 5 days thereafter (0.5 mg daily).The primary outcome was the level of cardiac troponin T (cTnT) at postoperative 48 h. The secondary outcomes included troponin I (cTnI) and creatine kinase-MB (CK-MB), inflammatory biomarkers (procalcitonin and interleukin-6, etc.), and adverse events (30-day mortality, stroke, ECMO and IABP use, etc.).
Results:
A total of 132 patients underwent non-CAGB cardiac surgery, 11were excluded because of diarrhea (n = 6) and long aortic cross-clamp time > 2 h (n = 5), 59 were assigned to the colchicine group and 62 to the placebo group. Compared with the placebo group, cTnT (median: 0.3 μg/L, IQR 0.2-0.4 μg/L vs. median: 0.4 μg/L, IQR 0.3-0.6 μg/L, P < 0.01), cardiac troponin I (median: 0.9 ng/ml, IQR 0.4-1.7 ng/ml vs. median: 1.3 ng/ml, IQR 0.6-2.3 ng/ml, P = 0.02), CK-MB (median: 1.9 ng/ml, IQR 0.7-3.2 ng/ml vs. median: 4.4 ng/ml, IQR 1.5-8.2 ng/ml, P < 0.01), and interleukin-6 (median: 73.5 pg/ml, IQR 49.6-125.8 pg/ml vs. median: 101 pg/ml, IQR 57.5-164.7 pg/ml, P = 0.048) were significantly reduced in colchicine group at postoperative 48 h. For safety evaluation, the colchicine (n = 65) significantly decreased post-pericardiotomy syndrome (3.08% vs. 17.7%, P < 0.01) and increased the rate of diarrhea (9.23% vs. 0, P = 0.01) compared with the placebo group (n = 62). No significant difference was observed in other adverse events between the two groups.
Conclusion:
A short perioperative course of low-dose colchicine was effective to attenuate the postoperative biomarkers of myocardial injury and inflammation, and to decrease the postoperative syndrome compared with the placebo. Trial registration ChiCTR2000040129. Registered 22nd Nov. 2020. This trial was registered before the first participant was enrolled. http://www.chictr.org.cn/showproj.aspx?proj=64370 .
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