Drug-eluting stent (DES)-based primary percutaneous intervention (pPCI) has been established as the standard of care for patients presenting with ST-segment elevation myocardial infarction (STEMI), having demonstrated superiority over thrombolysis, plain balloon angioplasty, and bare-metal stents. Recently, the use of drug-coated balloons (DCB) has expanded dramatically across a variety of anatomical and clinical settings, including de novo coronary lesions. A DCB-based pPCI strategy may simplify the procedure and mitigate the risks of inadequate stent sizing due to spasm or large thrombus burden, acute stent thrombosis, distal embolization, no reflow, and the relatively higher incidence of late stent-related adverse events compared with elective PCI. Despite these theoretical advantages, data on the safety and efficacy of DCB-based pPCI in STEMI remains limited. The aim of this registry is to explore procedural and clinical outcomes of patients with STEMI treated with a DCB-based pPCI strategy.
Study Type
OBSERVATIONAL
Enrollment
300
Provisional DCB-based pPCI for a de novo coronary
Universitatsklinikum AKH wien
Vienna, Austria
RECRUITINGNet adverse clinical events (NACE)
Composite of :Device success, Procedural success, Angiographic success diameter stenosis \<40% by visual estimation and TIMI flow grade ≥2, Target vessel dissection ≥ type C, Bailout stenting
Time frame: From January 2014 to April 2026
Individual NACE components
Time frame: Jenuary 2014 to April 2026
Any Bleeding
Any bleeding classified according to the Bleeding Academic Research Consortium (BARC) criteria.
Time frame: January 2014- April 2026
Target Vessel Failure (TVF)
Composite of cardiovascular death, target vessel myocardial infarction, or target vessel revascularization, according to Academic Research Consortium drug-coated balloon consensus definitions.
Time frame: January 2014-April 2026
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