Colchicine Prevents Myocardial Injury After Non-Cardiac Surgery Pilot Study (COPMAN)
试验速览
- 阶段
- 不适用
- 状态
- 撤回
- 试验地点
- 1
- 主要终点
- Number of Patients Recruited
研究概览
简要总结
Perioperative Myocardial Infarction (PMI) is a major contributor to perioperative mortality and morbidity with overall incidence of 5-16%. It is associated with increased 30-day mortality of 11.6% vs 2.2% of patients without PMI in non-cardiac surgical patients. However, its recognition and diagnosis remains challenging as the typical symptoms and findings of ischemic MI may be masked by post-operative changes and pain management.
In this study, the investigators hope to determine if colchicine decreases the incidence of MINS in high risk surgical patients undergoing non-cardiac surgery and optimally establish colchicine as a viable therapy to improve perioperative cardiovascular outcome in those patients.
详细描述
Perioperative Myocardial Infarction (PMI) is a major contributor to perioperative mortality and morbidity with overall incidence of 5-16%. It is associated with increased 30-day mortality of 11.6% vs 2.2% of patients without PMI in non-cardiac surgical patients. However, its recognition and diagnosis remains challenging as the typical symptoms and findings of ischemic MI may be masked by post-operative changes and pain management.
To support early detection and diagnosis of myocardial injury in the perioperative setting, myocardial injury after non-cardiac surgery (MINS) has been recognized as an important prognostic marker independently associated with mortality and significant morbidity in the perioperative period. MINS is defined as prognostically relevant myocardial injury due to ischemia that occurs during or within 30 days after noncardiac surgery. Perioperative screening and monitoring of MINS is recommended by the most recent 2016 Canadian Cardiovascular Society (CCS) Guidelines. One study found of the MINS patients, only 41.8% of which filled universal definition of MI. This may suggest that screening for MINS in the Perioperative setting by detecting post-operative troponin rise is an important marker to prompt further investigation and closer monitoring.
However, despite efforts in recognition and establishment of MINS, there is still no consensus for the optimal management of MINS in addition to routine cardiac risk stratification. Common MI management options may be complicated by post-operative changes such as anemia, hypotension, hypoxemia, and use of routine anti-platelet and anticoagulation agents and invasive intervention is associated with high risk of complication and mortality in the perioperative period.
Colchicine is an alkaloid anti-inflammatory drug with well-established safety and adverse effect profile in various clinical settings including pericarditis and gout flare. Pharmacologically, colchicine inhibits beta-tubulin polymerization into microtubules, preventing activation and migration of neutrophils to achieve its anti-inflammatory effect. Clinically in the cardiac surgery patient population, colchicine has been shown in multiple meta-analyses to be efficacious in preventing post-operative atrial fibrillation, in treatment and prevention of pericarditis and post-pericardiotomy syndrome. In patients who are high risk for cardiovascular events, systemic review has shown reduction in cardiovascular mortality and myocardial infarction in some studies. Colchicine is an ideal agent in the perioperative period as it does not increase the risk of major bleeding, hepatic and renal toxicity, and there is only gastrointestinal discomfort at high doses.
In this study, the investigators hope to determine if colchicine decreases the incidence of MINS in high risk surgical patients undergoing non-cardiac surgery and optimally establish colchicine as a viable therapy to improve perioperative cardiovascular outcome in those patients.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- Triple (Participant, Care Provider, Investigator)
盲法说明
Double-Blinded
入排标准
- 年龄范围
- 45 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Any patient undergoing non-cardiac surgery is eligible if (s)he is:
- •Aged 45 years of age or older
- •Expected to be admitted for >48 hours
- •Have a preoperative Brain natriuretic peptide (BNP) value of 92 or higher, or a N-terminal prohormone brain natriuretic peptide (NT-proBNP) value of 300 or higher,
- •If a BNP or NT-proBNP is not available, then the patient must fulfill at least one of the criteria for moderate to high risk of perioperative myocardial injury (see below):
- •Moderate to high risk for perioperative myocardial injury criteria:
- •History of coronary artery disease
- •History of peripheral artery disease
- •History of stroke
- •Undergoing major vascular surgery
- •Any 3 of the following 9 criteria:
- •Age 70 years or greater
- •Undergoing intraperitoneal, retroperitoneal, intrathoracic, or major orthopaedic surgery
- •History of heart failure
- •History of transient ischemic attack
- •History of diabetes requiring insulin or oral hypoglycemic medications
- •Hypertension
- •Serum creatinine greater than 170 mmol/mL
- •History of smoking within 2 years of surgery
- •Undergoing urgent or emergent surgery
排除标准
- •Patients will be ineligible for the study if (s)he has:
- •An allergy to colchicine
- •Myelodysplastic syndrome
- •An estimated glomerular filtration rate (eGFR) of less than 30 mL/min/1.73m2
- •Anticipated post-operative administration of cyclosporine, ketoconazole, itraconazole, protease inhibitors, or clarithromycin
研究组 & 干预措施
Colchicine Group
Administration of oral colchicine at 0.6 mg 1 hour prior to surgery, then 0.6 mg twice daily starting on the night after surgery for 7 days or until discharge from hospital, whichever occurs earlier. For patient under 60kg in body weight, daily dose will be 0.6 mg once daily. Medical and surgical management of the participant will be carried out under each institute's standard clinical practice.
干预措施: Colchicine 0.6 mg (Drug)
Placebo Group
Participants allocated to the control group will receive a placebo pill at the same dosing regimen as with treatment group. Perioperative and surgical care will not be different from standard clinical practice.
干预措施: Placebo oral tablet (Drug)
结局指标
主要结局
Number of Patients Recruited
时间窗: 3 months
The number of eligible subjects recruited in 3 months after 2 weeks of run-in period in participating centres
次要结局
- Incidence of Myocardial Injury after Non-Cardiac Surgery (MINS)(From Post-Operatively day one up to 7 days post-operatively)
- Adverse Events(Duration of hospital admission up to 7 days post-operatively)
- Incidence of premature discontinuation of the study drug and Reasoning(Post-Operatively until date of study drug discontinuation (up to 7 days post-operatively))
- Incidence of infectious complications(Duration of hospital admission up to 7 days post-operatively)
研究者
Ron Ree
Clinical Associate Professor
University of British Columbia
