Abstract

Objectives We analyzed the efficacy of drug coated balloons (DCB) as a stand-alone-therapy in de novo lesions of large coronary arteries. DCBs seem to be an attractive alternative for the stent-free interventional treatment of de novo coronary artery disease (CAD). However, data regarding a DCB-only approach in de novo CAD are currently limited to vessels of small caliber. Methods By means of propensity score (PS) matching 234 individuals with de novo CAD were identified with similar demographic characteristics. This patient population was stratified in a 1:1 fashion according to a reference vessel diameter cut-off of 2.75 mm in small and large vessel disease. The primary endpoint was the rate of clinically driven target lesion revascularization (TLR) at 9 months. Results Patients with small vessel disease had an average reference diameter of 2.45 ± 0.23 mm, while the large vessel group averaged 3.16 ± 0.27 mm. Regarding 9-month major adverse cardiac event (MACE), 5.7% of the patients with small and 6.1% of the patients with large vessels had MACE (p=0.903). Analysis of the individual MACE components revealed a TLR rate of 3.8% in small and 1.0% in large vessels (p=0.200). Of note, no thrombotic events in the DCB treated coronary segments occurred in either group during the 9-month follow-up. Conclusions Our data demonstrate for the first time that DCB-only PCI of de novo lesions in large coronary arteries (>2.75 mm) is safe and as effective. Interventional treatment for CAD without permanent or temporary scaffolding, demonstrated a similar efficacy for large and small vessels.

Highlights

  • Metallic stents are still the standard of care for percutaneous coronary interventions (PCI)

  • We believe that the low target lesion revascularization (TLR) rates after drug coated balloons (DCB)-only angioplasty in our patients with de novo lesions in large coronary arteries can be explained by the combination of proper lesion preparation, adequate DCB handling, and restrictive additional stent implantation

  • We are of the opinion that a 9-month cardiac death rate of 3% is an anticipated finding under the given clinical circumstances in our study population

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Summary

Introduction

Metallic stents are still the standard of care for percutaneous coronary interventions (PCI). Such permanent metallic implants can lead to chronic inflammation within the vessel wall and induce neoatherosclerosis which may explain an ongoing risk for target lesion failure (TLF) after stent implantation [1]. An interventional strategy to exclusively dilate coronary lesions without permanently caging the vessel seems to be very promising. The recently published clinical endpoint trial BASKET SMALL [6] revealed that, in patients with de novo lesion of reference vessel diameter

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