Key result
Type C lesions linked to ~83% higher MACE risk with drug-coated balloons, driven by TVR.
Why the study?
DCBs have emerged for PCI of in-stent restenosis or particular anatomical subsets, prompting a real-world evaluation of prognostic determinants and long-term outcomes across any lesion type.
Observational (n=267)
Yes
In real-world practice, drug-coated balloons are a viable option for coronary lesions, though type C and restenotic lesions carry a higher risk of MACE and target lesion failure.
Type C lesions may warrant caution with drug-coated balloons; leaves open optimal lesion selection in prospective trials.
Drug-coated balloons (DCBs) have emerged for percutaneous coronary interventions (PCI) of in-stent restenosis or particular anatomical subsets. We provide a real-world analysis of the prognostic determinants and long-term outcomes of patients treated with DCB for any lesion in a comprehensive multicenter registry. The primary study endpoint was the occurrence of major cardiovascular events (MACE: composite of all-cause death, myocardial infarction, and target vessel revascularization) at the longest available follow-up. We included 267 patients (196 treated for in-stent restenosis and 71 for de novo lesions), with a median follow-up of 616 [368–1025] days. MACE occurred in 70 (26.2%) of the patients and related with higher rates of in-stent restenosis (P = .04), longer and more type C lesions ( P = .05 and P = .04). At multivariate Cox-regression, type C lesions emerged as the only independent predictor of MACE (adjusted OR [95% CI] = 1.83[1.13–2.97], P = .014), mainly driven by target vessel revascularization (adjusted OR[95% CI] = 1.78[1.05–2.95], P = .03) not conditioning survival. In-stent restenosis emerged as major determinant of TLF (adjusted OR[95% CI] = 2.59[1.17–5.75], P = .02). DCBs represent a treatment option for any lesion; however, type C and restenotic lesions are associated with an increased risk of MACE and target lesion failure, where the optimal strategies for patients’ selection and lesion preparation are still undefined.
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Verdoia et al. (2022) conducted an observational in In-stent restenosis and de novo coronary lesions (n=267). Drug-coated balloons (DCB) was evaluated on Major cardiovascular events (MACE: composite of all-cause death, myocardial infarction, and target vessel revascularization) (adjusted OR 1.83, 95% CI 1.13-2.97, p=0.014). In patients treated with drug-coated balloons, type C lesions were an independent predictor of MACE (adjusted OR 1.83; 95% CI 1.13-2.97; P=0.014), mainly driven by target vessel revascularization.
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