Abstract

Background: Interventional treatment of aorto-ostial coronary stenoses is limited by stent recoil and suboptimal angiographic results, leading to restenosis and frequent re-interventions. As a potential bail-out strategy for stent recoil, implantation of an additional stent to increase radial force has been reported. Thus, we sought to investigate clinical outcomes after additional implantation of a Dynamic Renal® stent (DRS), a non-coronary; bare-metal stent with very high radial force, in aorto-ostial coronary stenoses. Methods: Patients treated by implantation of DRSs for stent recoil in the ostial right coronary artery or the left main stem were identified from the hospital database. Baseline clinical and procedural characteristics were compared to patients who underwent re-intervention for in-stent-restenosis in similar segments by either implantation of conventional drug-eluting stents (DES) or paclitaxel-coated balloons (PCB). Clinical follow-ups were performed up to three years following re-intervention with the assessment of death, target lesion reintervention (TLR), and major adverse cardiac events (MACE) as a combination death, myocardial infarction and target vessel revascularization. Kaplan–Meier analyses were performed for event-free survival between the three groups. Results: Between 05/2013 and 07/2019, 28 patients underwent DRS implantation of aorto-ostial coronary lesions. In comparison with 49 patients with DES implantation and 29 patients undergoing PCB treatment, no relevant differences in baseline parameters were identified. Median follow-up was 714 days, with an available follow-up of >1 year after intervention in 82.1% of patients. In the entire study cohort at two years after re-intervention, the TLR rate was 16% (17 patients), the MACE rate 37% (39 patients), and all-cause mortality 9% (10 patients), with no significant differences between the three groups. Conclusions: DRS implantation for treating stent recoil of aorto-ostial coronary lesions resulted in a high rate of TLR, and was associated with similar risk for death and MACE compared to treatment of in-stent-restenosis with DES or PCB. Randomized, larger comparisons of contemporary DES in patients exclusively presenting with stent recoil are necessary to further define the efficacy and safety of this approach.

Highlights

  • Aorto-ostial coronary lesions such as stenosis of the ostial right coronary artery or the ostial left main stem have been recognized as challenging targets for percutaneous coronary intervention (PCI)due to an increased risk of restenosis which can be caused by stent recoil [1]

  • Long-term outcomes of PCI in aorto-ostial coronary lesions with drug-eluting stents (DES) is less favorable compared to the results of PCI in non-ostial lesions [5,6]

  • This study reports for the first time the use of a bare-metal stent with very high radial strength, the Dynamic Renal stent, as a second stent for lesions with observed stent recoil

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Summary

Introduction

Aorto-ostial coronary lesions such as stenosis of the ostial right coronary artery or the ostial left main stem have been recognized as challenging targets for percutaneous coronary intervention (PCI). The Dynamic Renal Stent® (DRS, Biotronik, Berlin, Germany) is a bare metal stent with high radial force due to a cobalt-chromium alloy and struts of 120 μm thickness, thicker than struts of contemporary Resolute OnyxTM (81 μm for diameters ≤ 4.0 mm and 91 μm for diameters ≥ 4.5 mm) or Synergy MegatronTM (89 μm) DES. It was developed for the use in renal arteries, known for frequent recoil after angioplasty. The present study reports the clinical outcomes of patients that underwent implantation of a DRS as a second stent strategy in aorto-ostial lesions

Study Population
Collection of Data
Clinical Outcomes according to Treatment Strategy
Findings
Discussion
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