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Updated: Mar 13, 2026

Imaging In-Stent Restenosis: An Inexpensive, Reliable, and Rapid Preclinical Model
Published on: September 14, 2009
Initial clinical experience of CrossBoss catheter for in-stent chronic total occlusion lesions: A case report
Lei Zhao1, Long-Bo Li, Zhi-Hui Wang
1Department of Cardiology, Second Hospital of Jilin University, Changchun, Jilin Province, China.
Insights
The CrossBoss catheter shows a 75% success rate for treating in-stent chronic total occlusions (CTOs), demonstrating safety and efficacy in this challenging condition. This study recommends the device for complex in-stent CTO interventions.
Area of Science:
- Interventional Cardiology
- Vascular Access Technologies
- Cardiovascular Disease Management
Background:
- Chronic total occlusions (CTOs) within previously placed stents present a significant challenge in interventional cardiology.
- Existing data on crossing catheters for CTOs do not specifically address in-stent CTOs.
Observation:
- The CrossBoss catheter was utilized in 8 patients with in-stent CTO lesions.
- A retrospective review of clinical data was performed to assess the efficacy and safety of the CrossBoss system.
Findings:
- The CrossBoss catheter achieved a 75% success rate (6 out of 8 patients) in crossing in-stent CTO lesions.
- No complications were reported in any of the treated patients, indicating a favorable safety profile.
- Higher Japan chronic total occlusion scores correlated with a lower success rate.
Implications:
- The CrossBoss catheter is a safe and effective tool for managing challenging in-stent CTO lesions.
- This technology offers a promising solution for improving procedural success in complex coronary interventions.
- Further research may explore optimizing its use in patients with higher CTO complexity scores.
Background:
The CrossBoss coronary chronic total occlusion (CTO) crossing catheter has been demonstrated to have greatly improved the success rate of crossing CTO lesions, but there are no published data on its application for in-stent CTO lesions.
Methods:
In the current study, we retrospectively reviewed the clinical data of 8 patients with in-stent CTO lesions that were managed with the CrossBoss catheter and herein we report the efficacy and safety of the CrossBoss crossing and re-entry system for this clinically challenging condition.
Results:
The CrossBoss catheter was used for 8 patients with in-stent CTO lesions, which resulted in success in 6 cases and failure in 2 cases, with a 75% success rate. Of the 6 patients with successful treatment, 5 cases had the occlusive lesions crossed with the CrossBoss catheter through a proximal lumen-to-distal lumen approach, whereas the remaining case had his occlusive lesions penetrated by the CrossBoss catheter and the guidewire. Two cases failed in treatment as the CrossBoss catheter could not cross the occlusive lesions. The 6 cases with successful treatment included 3 cases with occlusive lesions in the left anterior descending artery, 1 case with occlusive lesions in the obtuse marginal branches, and 2 cases with occlusive lesions in the right coronary artery, and the 2 cases with failure in treatment had their occlusive lesions in the right coronary artery. In addition, patients with a higher Japan chronic total occlusion score were found to have a lower success rate of crossing the occlusive lesions. None of the patients developed complications.
Conclusion:
Our study demonstrates that the CrossBoss catheter has a high success rate and is safe for in-stent CTOs and can be recommended for this rather clinically challenging condition.
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