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Published on: September 22, 2020
Randomized trial of preventive angioplasty in myocardial infarction
David S Wald1, Joan K Morris, Nicholas J Wald
1Wolfson Institute of Preventive Medicine, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom. d.s.wald@qmul.ac.uk
Insights
Preventive percutaneous coronary intervention (PCI) in non-infarct arteries significantly lowers adverse cardiovascular events in ST-segment elevation myocardial infarction (STEMI) patients. This strategy is more effective than treating only the culprit artery during STEMI.
Area of Science:
- Cardiology
- Interventional Cardiology
- Acute Coronary Syndromes
Background:
- ST-segment elevation myocardial infarction (STEMI) management typically involves percutaneous coronary intervention (PCI) of the infarct artery.
- The benefit of performing PCI on non-infarct arteries with significant blockages (preventive PCI) in STEMI patients remains unclear.
Purpose of the Study:
- To evaluate the efficacy of preventive PCI in non-infarct arteries for patients with STEMI and multivessel coronary artery disease.
Main Methods:
- A randomized controlled trial involving 465 STEMI patients undergoing infarct-artery PCI.
- Patients were assigned to either preventive PCI in non-infarct arteries or infarct-artery-only PCI.
- The primary outcome was a composite of cardiac death, nonfatal myocardial infarction, or refractory angina.
Main Results:
- Preventive PCI significantly reduced the primary outcome by 65% compared to infarct-artery-only PCI (9 vs. 23 events per 100 patients).
- Hazard ratios favored preventive PCI for cardiac death (0.34), nonfatal myocardial infarction (0.32), and refractory angina (0.35).
- The trial was stopped early due to conclusive evidence favoring preventive PCI.
Conclusions:
- In STEMI patients with multivessel disease, preventive PCI in non-infarct arteries substantially decreases the risk of major adverse cardiovascular events.
- PCI limited to the infarct artery is less effective than a strategy including preventive PCI for non-infarct arteries.
Background:
In acute ST-segment elevation myocardial infarction (STEMI), the use of percutaneous coronary intervention (PCI) to treat the artery responsible for the infarct (infarct, or culprit, artery) improves prognosis. The value of PCI in noninfarct coronary arteries with major stenoses (preventive PCI) is unknown.
Methods:
From 2008 through 2013, at five centers in the United Kingdom, we enrolled 465 patients with acute STEMI (including 3 patients with left bundle-branch block) who were undergoing infarct-artery PCI and randomly assigned them to either preventive PCI (234 patients) or no preventive PCI (231 patients). Subsequent PCI for angina was recommended only for refractory angina with objective evidence of ischemia. The primary outcome was a composite of death from cardiac causes, nonfatal myocardial infarction, or refractory angina. An intention-to-treat analysis was used.
Results:
By January 2013, the results were considered conclusive by the data and safety monitoring committee, which recommended that the trial be stopped early. During a mean follow-up of 23 months, the primary outcome occurred in 21 patients assigned to preventive PCI and in 53 patients assigned to no preventive PCI (infarct-artery-only PCI), which translated into rates of 9 events per 100 patients and 23 per 100, respectively (hazard ratio in the preventive-PCI group, 0.35; 95% confidence interval [CI], 0.21 to 0.58; P<0.001). Hazard ratios for the three components of the primary outcome were 0.34 (95% CI, 0.11 to 1.08) for death from cardiac causes, 0.32 (95% CI, 0.13 to 0.75) for nonfatal myocardial infarction, and 0.35 (95% CI, 0.18 to 0.69) for refractory angina.
Conclusions:
In patients with STEMI and multivessel coronary artery disease undergoing infarct-artery PCI, preventive PCI in noninfarct coronary arteries with major stenoses significantly reduced the risk of adverse cardiovascular events, as compared with PCI limited to the infarct artery. (Funded by Barts and the London Charity; PRAMI Current Controlled Trials number, ISRCTN73028481.).
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