The Safety and Efficacy of Femoral Access Versus Radial for Primary Percutaneous Coronary Intervention in ST-Elevation Myocardial Infarction (SAFARI-STEMI Trial)
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 2,292
- 试验地点
- 10
- 主要终点
- All-cause mortality
研究概览
简要总结
Primary percutaneous coronary intervention (PPCI) has become the dominant strategy for the treatment of ST-elevation myocardial infarction (STEMI), as studies have shown that PPCI is superior to fibrinolytic therapy. Recent evidence suggests that transradial access (TRA) is superior to transfemoral (TFA) for patients undergoing PPCI. Two large trials report a mortality benefit favouring TRA. The results of these two trials could significantly impact practice guidelines and lead to a recommendation that the approach of choice for primary PCI be radial rather than femoral. This would have significant implications for both PCI centers and interventionalists associated with a large impact on practice and education. Yet, many centers and interventionalists in Canada and in the USA prefer TFA and currently feel pressured in making the change to TRA. With that said, these trials did not include new pharmacotherapy and new technology that would likely have closed or eliminated the gap between TFA and TRA by improving the safety and efficacy of these two approaches. Furthermore, these trials were not powered to conclusively show a mortality benefit. The authors of the two large trials emphasized the need for further trials to confirm the benefits of TRA.
The SAFARI-STEMI trial aims to compare TFA with TRA in patients undergoing primary percutaneous intervention (PPCI). The primary outcome will be defined as all cause mortality measured at 30 days. The trial will also evaluate: 1) bleeding events and 2) the composite of death, reinfarction, or stroke defined as major adverse clinical events (MACE). The trial will include the use of antithrombotic therapy with monotherapy, with either bivalirudin or unfractionated heparin; the use of glycoprotein inhibitors IIb/IIIa inhibitors will be avoided. The study will encourage liberal use of vascular closing devices. The trial will also compare delays to reperfusion between the two strategies. Finally, a cost analysis is proposed.
In view of recent publications, there is now a need for a large randomized trial using contemporary adjunct therapies to assess the safety and efficacy of the TRA vs. the TFA in PPCI. The proposed trial aims to conclusively show whether there is a survival benefit associated with the TRA approach.
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
- None
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Ischemic chest discomfort of greater or equal to 30 minutes duration,
- •Onset of chest pain of greater or equal to 12 hrs prior to entry into the study,
- •ST segment elevation of > 1 mm (0.1 mV) in two or more contiguous electrocardiographic leads (on a standard 12 lead ECG) or left bundle branch block not known to be old
排除标准
- •Age < 18 yrs
- •Active bleeding
- •Inadequate vascular access from the femoral arteries (i.e. severe peripheral vascular artery disease precluding right or left femoral approach)
- •Abnormal Allen's test precluding either right or left radial approach
- •PCI within the last 30 days
- •Fibrinolytic agents within the last 7 days
- •Warfarin, dabigatran or other oral anticoagulant within the last 7 days
- •Known coagulation disorder (i.e. INR >2.0, platelets <100,000 / mm3)
- •Allergy to aspirin
- •Participation in a study with another investigational device or drug < four weeks
- •Known severe renal impairment (creatinine >200 umol/L)*
- •Known severe contrast (dye) allergy
- •Prior coronary artery bypass surgery
- •Inability to provide informed consent
- •Bivalirudin is contraindicated in renal failure.
研究组 & 干预措施
TFA
Transfemoral Access
干预措施: Primary Percutaneous Coronary Intervention (PPCI) (Procedure)
TRA
Transradial Access
干预措施: Primary Percutaneous Coronary Intervention (PPCI) (Procedure)
结局指标
主要结局
All-cause mortality
时间窗: 30 days
The primary outcomes will be all-cause mortality measured at 30 days.
次要结局
- Bleeding(30 days)
- Length of Hospital Stay(Index hospitalization)
- Stroke(30 days and 6 months)
- Reinfarction(30 days and 6 months)
- Resource utilization(30 days)
- Stent thrombosis(30 days and 6 months)
- Critical time intervals (including door-to-balloon time)(Index hospitalization)
- All-cause mortality(6 months)
- Fluoroscopy time and radiation exposure(Index Catheterization)
- Death, reinfarction, or stroke(30 days and 6 months)
- Number of blood transfusions(30 days)
- Cardiogenic shock(30 days)
研究者
Michel Le May
Director of Regional ACS Programs
Ottawa Heart Institute Research Corporation
