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Updated: Sep 9, 2025

Optimized Management of Endovascular Treatment for Acute Ischemic Stroke
Published on: January 18, 2018
Immediate versus staged complete revascularisation during index admission in patients with ST-segment elevation
Min Chul Kim1, Joon Ho Ahn1, Dae Young Hyun1
1Division of Cardiology, Department of Internal Medicine, Chonnam National University Hospital, Chonnam National University Medical School, Chonnam National University, Gwangju, South Korea.
Insights
Immediate complete revascularisation was not superior to staged procedures for ST-segment elevation myocardial infarction (STEMI) patients with multivessel disease. This finding impacts guidelines for revascularisation timing in STEMI care.
Area of Science:
- Cardiology
- Interventional Cardiology
- Clinical Trials
Background:
- Optimal timing for complete revascularisation in ST-segment elevation myocardial infarction (STEMI) with multivessel coronary artery disease is not well-defined.
- Current practices vary regarding immediate versus staged revascularisation during the index hospitalisation for STEMI patients.
Purpose of the Study:
- To evaluate if immediate complete revascularisation is non-inferior to staged complete revascularisation in STEMI patients with multivessel disease.
- To compare the composite endpoint of death, non-fatal myocardial infarction, or unplanned revascularisation at 1 year between the two strategies.
Main Methods:
- An open-label, randomised, non-inferiority trial involving 994 patients across 14 South Korean hospitals.
- Patients with STEMI and multivessel disease were randomised to either immediate or staged percutaneous coronary intervention (PCI) for non-culprit lesions.
- The primary endpoint was assessed at 1 year using an intention-to-treat analysis with a non-inferiority margin set at a hazard ratio of 1.42.
Main Results:
- The primary endpoint occurred in 13% of the immediate group versus 11% in the staged group (Hazard Ratio: 1.24; 95% CI: 0.86-1.79), failing to meet non-inferiority criteria (p=0.24).
- Rates of stroke, major bleeding, and contrast-induced nephropathy were similar between groups.
- Cardiogenic shock during index hospitalisation was more frequent in the immediate revascularisation group (4%) compared to the staged group (2%).
Conclusions:
- Immediate complete revascularisation was not demonstrated to be non-inferior to staged revascularisation for the composite endpoint in STEMI patients with multivessel disease at 1 year.
- The findings suggest that current clinical guidelines may need to be informed regarding the optimal timing of complete revascularisation in this patient population.
- Further long-term follow-up is ongoing to assess the complete clinical impact of both strategies.
Background:
The optimal timing of complete revascularisation for patients with ST-segment elevation myocardial infarction (STEMI) and multivessel coronary artery disease remains unclear. We aimed to assess whether immediate complete revascularisation was non-inferior to staged complete revascularisation during the index admission.
Methods:
We conducted an open-label, randomised, non-inferiority trial at 14 hospitals in South Korea. Patients aged 19 years or older with STEMI and multivessel disease who had undergone percutaneous coronary intervention (PCI) for a culprit lesion were randomly assigned 1:1 to immediate complete revascularisation (PCI for non-culprit lesions during the index procedure) or staged complete revascularisation (non-culprit PCI on another day during the index admission). Web-based, permuted-block randomisation (using mixed block sizes of two or four) was implemented at each participating centre to allocate patients. Non-culprit lesions with 50-69% stenosis were evaluated by fractional flow reserve. Study participants and study investigators were aware of treatment allocation, but members of the independent clinical committee reviewing primary and secondary endpoints were masked to treatment allocation. The primary endpoint was a composite of death from any cause, non-fatal myocardial infarction, or any unplanned revascularisation at 1 year in the intention-to-treat population, and the non-inferiority margin was set at a hazard ratio (HR) of 1·42; if the upper boundary of the one-sided 97·5% CI of the HR was less than 1·42, immediate complete revascularisation would be considered non-inferior to staged complete revascularisation. Reported adverse events consisted of procedural complications, other complications during admission, and in-hospital clinical events occurring during the index admission. This trial is registered with the Clinical Research Information Service (KCT0004457) and ClinicalTrials.gov (NCT04626882). Long-term follow-up is ongoing.
Findings:
Between Dec 30, 2019, and Jan 15, 2024, 994 patients were enrolled and randomly assigned to immediate revascularisation (n=498; immediate group) or staged revascularisation (n=496; staged group). The primary endpoint occurred at 1 year in 65 patients (13%) in the immediate group and 53 patients (11%) in the staged group (HR 1·24 [95% CI 0·86-1·79]; pnon-inferiority=0·24). Rates of stroke, major bleeding, and contrast-induced nephropathy did not differ significantly between the two groups. Cardiogenic shock during the index hospitalisation occurred in 18 (4%) of 498 patients in the immediate group and nine (2%) of 496 patients in the staged complete revascularisation group.
Interpretation:
Among patients with STEMI and multivessel disease, immediate complete revascularisation was not shown to be non-inferior to staged complete revascularisation during the index admission in terms of incidence of a composite of death from any cause, non-fatal myocardial infarction, or any unplanned revascularisation at 1 year. This finding might inform future clinical guidelines on the role and optimal use of immediate complete revascularisation during the index admission.
Funding:
Boston Scientific.
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