Publication:
Stepwise provisional versus systematic culotte for stenting of true coronary bifurcation lesions: five-year follow-up of the multicentre randomised EBC TWO Trial

dc.contributor.authorArunothayaraj, Sandeep (36140221200)
dc.contributor.authorBehan, Miles W. (8862299400)
dc.contributor.authorLefèvre, Thierry (13608617100)
dc.contributor.authorLassen, Jens F. (57189389659)
dc.contributor.authorChieffo, Alaide (57202041611)
dc.contributor.authorStankovic, Goran (59150945500)
dc.contributor.authorBurzotta, Francesco (7003405739)
dc.contributor.authorPan, Manuel (7202544866)
dc.contributor.authorFerenc, Miroslaw (8933716300)
dc.contributor.authorHovasse, Thomas (25627893900)
dc.contributor.authorSpence, Mark S. (7103007124)
dc.contributor.authorBrunel, Philippe (7006007671)
dc.contributor.authorCotton, James M. (7102218822)
dc.contributor.authorCockburn, James (43661048500)
dc.contributor.authorCarrié, Didier (7006798967)
dc.contributor.authorBaumbach, Andreas (56962775900)
dc.contributor.authorMaeng, Michael (20034699800)
dc.contributor.authorLouvard, Yves (7004523655)
dc.contributor.authorHildick-Smith, David (8089365300)
dc.date.accessioned2025-06-12T12:10:03Z
dc.date.available2025-06-12T12:10:03Z
dc.date.issued2023
dc.description.abstractBackground: The multicentre European Bifurcation Club Trial (EBC TWO) showed no significant differences in 12-month clinical outcomes between patients randomised to a provisional stenting strategy or systematic culotte stenting in non-left main true bifurcations. Aims: This study aimed to investigate the 5-year clinical results of the EBC TWO Trial. Methods: A total of 200 patients undergoing stent implantation for non-left main bifurcation lesions were recruited into EBC TWO. Inclusion criteria required a side branch diameter ≥2.5 mm and side branch lesion length >5 mm. Five-year follow-up was completed for 197 patients. The primary endpoint was the composite of all-cause mortality, myocardial infarction, or target vessel revascularisation. Results: The mean side branch stent diameter was 2.7±0.3 mm and mean side branch lesion length was 10.3±7.2 mm. At 5-year follow-up, the primary endpoint occurred in 18.4% of provisional and 23.7% of systematic culotte patients (hazard ratio [HR] 0.75, 95% confidence interval [CI]: 0.41-1.38). No significant differences were identified individually for all-cause mortality (7.8% vs 7.2%, HR 1.11, 95% CI: 0.40-3.05), myocardial infarction (8.7% vs 13.4%, HR 0.64, 95% CI: 0.27-1.50) or target vessel revascularisation (6.8% vs 9.3%, HR 1.12, 95% CI: 0.37-3.34). Stent thrombosis rates were also similar (1.9% vs 3.1%, HR 0.63, 95% CI: 0.11-3.75). There was no significant interaction between the extent of side branch disease and the primary outcome (p=0.34). Conclusions: In large non-left main true bifurcation lesions, the use of a systematic culotte strategy showed no benefit over provisional stenting for the composite outcome of all-cause mortality, myocardial infarction, or target vessel revascularisation at 5 years. The stepwise provisional approach may be considered preferable for the majority of true coronary bifurcation lesions. © Europa Digital & Publishing 2023. All rights reserved.
dc.identifier.urihttps://doi.org/10.4244/EIJ-D-23-00211
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85166100440&doi=10.4244%2fEIJ-D-23-00211&partnerID=40&md5=fcef12fa7abc2da55aa4cc04e103db09
dc.identifier.urihttps://remedy.med.bg.ac.rs/handle/123456789/2592
dc.subjectACS/NSTE-ACS
dc.subjectbifurcation
dc.subjectdrug-eluting stent
dc.subjectstable angina
dc.titleStepwise provisional versus systematic culotte for stenting of true coronary bifurcation lesions: five-year follow-up of the multicentre randomised EBC TWO Trial
dspace.entity.typePublication

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