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Published on: May 14, 2013
Coronary Stents in Patients with ST-Elevation Myocardial Infarction and Chronic Kidney Disease Undergoing Primary
Khurshid Ahmed1, Myung Ho Jeong, Rabin Chakraborty
1The Heart Center of Chonnam National University Hospital, Chonnam National University Research Institute of Medical Sciences, Gwangju, Korea. ; Apollo Gleneagles Hospital, Kolkata, India.
Insights
For patients with ST-elevation myocardial infarction and chronic kidney disease undergoing percutaneous coronary intervention, all five stent types showed similar 12-month risks for major adverse cardiac events. Further long-term studies are needed to confirm these findings.
Area of Science:
- Cardiology
- Nephrology
- Interventional Cardiology
Background:
- Chronic kidney disease (CKD) is linked to adverse outcomes following percutaneous coronary intervention (PCI).
- Optimal stent selection in STEMI patients with CKD remains an area of investigation.
Purpose of the Study:
- To compare the efficacy and safety of five different coronary stent types in patients with ST-elevation myocardial infarction (STEMI) and CKD undergoing primary PCI.
- To evaluate the 12-month incidence of major adverse cardiac events (MACE) across different stent categories.
Main Methods:
- A cohort of 2408 STEMI patients with CKD (eGFR <60 mL/min/1.73 m²) undergoing primary PCI were analyzed.
- Patients were stratified into five groups based on stent type: bare metal stent (BMS), paclitaxel-eluting stent (PES), sirolimus-eluting stent (SES), zotarolimus-eluting stent (ZES), and everolimus-eluting stent (EES).
- The primary endpoint was the occurrence of MACE at 12 months post-procedure.
Main Results:
- No significant differences were observed in myocardial infarction or target lesion/vessel revascularization rates among the stent groups.
- However, significant differences were noted in the overall rate of repeat revascularization and all-cause death.
- The 12-month MACE incidence varied: BMS (8.3%), PES (9.8%), SES (8.6%), ZES (5.5%), and EES (2.6%).
- Kaplan-Meier analysis and adjusted models did not reveal significant differences in 12-month MACE-free survival among the groups.
Conclusions:
- The study suggests that any of the five evaluated stent types may be suitable for STEMI patients with CKD undergoing primary PCI, with similar 12-month MACE risk.
- These findings are hypothesis-generating and underscore the need for long-term randomized trials to validate the comparative effectiveness of these stents in this high-risk population.
Background And Objectives:
Chronic kidney disease (CKD) is associated with poor outcomes after percutaneous coronary intervention (PCI). We sought to compare different coronary stents used during primary PCI in patients with ST-elevation myocardial infarction (STEMI) and CKD.
Subjects And Methods:
We selected 2408 consecutive STEMI patients with CKD (estimated glomerular filtration rate <60 mL/min/1.73 m(2)) undergoing primary PCI and divided them into 5 groups based on the type of stent implanted: 1) bare metal stent (BMS), 2) paclitaxel-eluting stent (PES), 3) sirolimus-eluting stent (SES), 4) zotarolimus-eluting stent (ZES), or 5) everolimus-eluting stent (EES). The study endpoint was the number of major adverse cardiac events (MACE) at 12 months.
Results:
There was no significant difference in the incidence of 12-month myocardial infarction, target lesion revascularization, or target vessel revascularization between stent groups; however, the overall rate of repeat revascularization differed significantly between groups. All-cause death differed significantly among the groups. The incidence of 12-month MACE in BMS, PES, SES, ZES, and EES was 8.3%, 9.8%, 8.6%, 5.5%, and 2.6%, respectively (p<0.001). Kaplan-Meier analysis did not show a significant differences in 12-month MACE-free survival among the groups (log-rank p=0.076). This finding remained the same after adjusting for multiple confounders (p=0.147).
Conclusion:
Any of the 5 stents can be used to treat STEMI patients with CKD undergoing primary PCI; all have similar risk of 12-month MACE. This result is hypothesis-generating and warrants further evaluation with a long-term randomized study.
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