Key result
PCI with a paclitaxel-eluting balloon yields an ~8% MACE rate over long-term follow-up.
Why the study?
Drug-eluting balloons are used in PCI, but their long-term results remain unknown.
Cohort (n=320)
No
In a real-world cohort, PCI with a second-generation paclitaxel-eluting balloon demonstrated a low MACE rate of 8% over a median 42-month follow-up for both de novo and in-stent restenosis lesions.
PCI with paclitaxel-eluting balloons was associated with low MACE in this cohort; hypothesis-generating and requires randomized confirmation.
Drug-eluting balloons currently constitute a therapeutic tool used in percutaneous coronary interventions (PCI). Long-term results remain unknown. We evaluated the prognosis of PCI using a second generation paclitaxel-eluting balloon (PEB) in real-world patients. We included all PCI with PEB in de novo or in-stent restenosis coronary lesions performed in our unit from March 2009 to March 2019. We assessed the composite of major adverse cardiovascular events (MACE) rate after a median follow-up of 42 months. Consecutive patients (n = 320) with 386 lesions were included; 46.9% presented with stable angina and 53.1% acute coronary syndromes; 52.6% of the lesions were in-stent restenosis and 47.3% de novo lesions with a mean diameter of 2.4 ± 0.5 mm. A bare metal stent was implanted in 6.7% and a drug-eluting stent in 8.5% of patients. The MACE rate was 8%: 10 (2.6%) cardiovascular deaths, 13 (3.4%) myocardial infarctions, and 16 (4.1%) target lesion revascularization. The all-cause death rate was 5.2%. No cases of thrombosis were recorded. In conclusion, PEB was a safe and effective tool to treat in-stent restenosis and de novo coronary lesions, especially small vessel disease, during long-term follow-up.
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Pérez et al. (2020) conducted a cohort in De novo or in-stent restenosis coronary lesions (n=320). Paclitaxel-eluting balloon (PEB) was evaluated on Major adverse cardiovascular events (MACE). Percutaneous coronary intervention using a paclitaxel-eluting balloon for coronary lesions resulted in an 8% major adverse cardiovascular event rate over a median 42-month follow-up.
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