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Colchicine in Patients With Recent Myocardial Infarction: A Systematic Review and Meta-Analysis of Randomized
Areesha Moiz1, Tetiana Zolotarova1, Mark J Eisenberg1,2,3,4,5
1Centre for Clinical Epidemiology, Lady Davis Institute, Jewish General Hospital McGill University Montreal QC Canada.
Insights
Colchicine did not significantly improve cardiovascular outcomes in patients with recent myocardial infarction. Further research is needed to clarify the role of this anti-inflammatory agent in post-myocardial infarction care.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Trials
Background:
- The efficacy of colchicine, an anti-inflammatory drug, in improving cardiovascular outcomes after myocardial infarction is not well-established.
- This study aimed to assess colchicine's effectiveness and safety compared to placebo in patients experiencing recent myocardial infarction.
Purpose of the Study:
- To evaluate the impact of colchicine on major adverse cardiovascular events (MACE) in patients who have recently had a myocardial infarction.
- To determine the safety profile of colchicine, including adverse events, in this patient population.
Main Methods:
- A systematic literature search was conducted across major databases (MEDLINE, Embase, Cochrane Library) for randomized controlled trials.
- Five randomized controlled trials involving 6,620 patients on colchicine and 6,625 on placebo were analyzed.
- The primary endpoint was MACE, with secondary endpoints including MACE components and safety outcomes, analyzed using random-effects models.
Main Results:
- No statistically significant difference in MACE was observed between the colchicine and placebo groups (8.2% vs. 9.3%).
- Analyses of individual MACE components did not yield conclusive results.
- Colchicine use did not lead to an increased incidence of overall or serious adverse events compared to placebo.
Conclusions:
- Current evidence suggests that colchicine, as an adjunct to standard therapy, does not conclusively impact MACE in patients with recent myocardial infarction.
- The available data, with a median follow-up of one year, remain insufficient to establish colchicine's definitive role in this clinical setting.
Background:
The role of colchicine, an anti-inflammatory agent, in improving cardiovascular outcomes in patients with recent myocardial infarction remains unclear. We sought to evaluate the efficacy and safety of colchicine compared with placebo in patients with recent myocardial infarction (within 1 month of symptom onset) at a follow-up of at least 1 year.
Methods:
We systematically searched MEDLINE, Embase, and the Cochrane Library until January 2025 for randomized controlled trials comparing colchicine to placebo in recent myocardial infarction. The primary outcome was major adverse cardiovascular events (MACE; as defined by the included studies) at maximum follow-up. Secondary outcomes included individual MACE components and safety (serious adverse events [AEs], any AEs, and gastrointestinal AEs). Count data were pooled using random-effects models with inverse variance weighting to estimate risk ratios (RRs) and 95% CIs.
Results:
A total of 5 randomized controlled trials were included with 6620 patients randomized to colchicine and 6625 to placebo. Most participants (79%) were male, with mean ages ranging from 59 to 61 years. Follow-up durations ranged from 1 to 3 years. At maximum follow-up, there was no statistically significant difference in MACE between colchicine and placebo (8.2% versus 9.3%; RR, 0.83 [95% CI, 0.66-1.04]). Analyses of individual MACE components were also inconclusive. Randomization to colchicine did not increase the overall incidence of AEs or serious AEs compared with placebo.
Conclusions:
In patients with recent myocardial infarction, the available evidence assessing the effect of colchicine, in addition to standard therapy, on MACE remains inconclusive over a median follow-up duration of 1 year.
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