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Published on: May 14, 2013
Drug-Coated Balloon-Based Versus Drug-Eluting Stent-Only Treatment in Patients With Chronic Kidney Disease
Eun-Seok Shin1, Yong Hoon Kim2, Dong Oh Kang3
1Department of Cardiology, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Republic of Korea.
Insights
Drug-coated balloon (DCB) percutaneous coronary intervention (PCI) significantly reduced major bleeding in chronic kidney disease (CKD) patients compared to drug-eluting stents (DES). This DCB-based PCI strategy offers a safer alternative for CKD patients undergoing PCI, with comparable cardiovascular event rates.
Area of Science:
- Cardiology
- Nephrology
- Interventional Cardiology
Background:
- Chronic kidney disease (CKD) elevates bleeding risk post-percutaneous coronary intervention (PCI).
- Limited evidence exists on drug-coated balloon (DCB) efficacy in CKD patients undergoing PCI.
- Drug-eluting stent (DES)-only PCI is a common treatment for coronary artery disease.
Purpose of the Study:
- To compare the 2-year major bleeding risk between DCB-based PCI and DES-only PCI in CKD patients.
- To evaluate major adverse cardiovascular events (MACE) as a secondary endpoint.
Main Methods:
- Retrospective analysis of 415 CKD patients undergoing DCB-based PCI.
- Propensity score matching (1:1) to a cohort of 415 CKD patients treated with DES-only PCI.
- CKD defined as estimated glomerular filtration rate (eGFR) <60 ml/min/1.73m².
- Primary endpoint: major bleeding at 2 years; Secondary endpoint: MACE.
Main Results:
- DCB-based PCI showed significantly lower major bleeding incidence (2.3% vs. 5.9%; HR: 0.41; P=0.030) at 2 years.
- MACE incidence was comparable between DCB-based PCI and DES-only PCI groups (10.7% vs. 13.0%; HR: 0.77; P=0.230).
- No target lesion thrombosis occurred in the DCB-based group, compared to five cases in the DES-only group.
- Multivariable analysis confirmed DCB-based PCI independently associated with reduced 2-year major bleeding risk.
Conclusions:
- DCB-based PCI significantly reduces major bleeding risk in CKD patients compared to DES-only PCI.
- DCB-based PCI demonstrates comparable MACE rates to DES-only PCI in this high-risk population.
- DCB-based PCI represents a potentially valuable strategy for mitigating bleeding complications in CKD patients undergoing PCI.
Abstract:
Chronic kidney disease (CKD) is associated with a high bleeding risk after percutaneous coronary intervention (PCI), but evidence on the efficacy of drug-coated balloon (DCB) treatment in this population remains limited. This study aimed to compare the bleeding risk of DCB-based PCI with that of drug-eluting stent (DES)-only PCI in patients with CKD. We retrospectively enrolled 415 consecutive patients with CKD who underwent DCB-based PCI and propensity score-matched them (1:1) to 415 patients who underwent conventional PCI with second-generation DES (DES-only group). CKD was defined as eGFR <60 mL/min/1.73 m2. The primary end point was the incidence of major bleeding at 2 years, and the secondary end point was major adverse cardiovascular events (MACE). Baseline characteristics were comparable between the two groups. In the DCB-based group, 65.1% of patients were treated with DCB-only. At 2-year, DCB-based PCI group showed a significantly lower incidence of major bleeding than DES-only group (2.3% vs 5.9%; hazard ratio 0.41; 95% confidence interval 0.19-0.92; p = 0.030), whereas the incidence of MACE was comparable between groups (10.7% vs 13.0%; hazard ratio 0.77; 95% confidence interval 0.50-1.18; p = 0.230). Five cases of target lesion thrombosis occurred in the DES-only group, but none in the DCB-based group. In multivariable analysis, DCB-based PCI was independently associated with a lower risk of 2-year major bleeding. In conclusion, among patients with CKD, DCB-based PCI was associated with a significantly lower risk of major bleeding compared with DES-only PCI, without a significant difference in MACE. These findings suggest that DCB-based PCI may be a viable strategy to reduce bleeding events in patients with CKD.
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