TY - JOUR
T1 - The EBC TWO Study (European Bifurcation Coronary TWO): A Randomized Comparison of Provisional T-Stenting Versus a Systematic 2 Stent Culotte Strategy in Large Caliber True Bifurcations
AU - Hildick-Smith, David
AU - Behan, Miles W.
AU - Lassen, Jens F.
AU - Chieffo, Alaide
AU - Lefèvre, Thierry
AU - Stankovic, Goran
AU - Burzotta, Francesco
AU - Pan, Manuel
AU - Ferenc, Miroslaw
AU - Bennett, Lorraine
AU - Hovasse, Thomas
AU - Spence, Mark S.
AU - Oldroyd, Keith
AU - Brunel, Philippe
AU - Carrie, Didier
AU - Baumbach, Andreas
AU - Maeng, Michael
AU - Skipper, Nicola
AU - Louvard, Yves
PY - 2016
Y1 - 2016
N2 - Background-For the treatment of coronary bifurcation lesions, a provisional strategy is superior to systematic 2-stent techniques for the most bifurcation lesions. However, complex anatomies with large side branches (SBs) with significant ostial disease length are considered by expert consensus to warrant a 2-stent technique upfront. This consensus view has not been scientifically assessed. Methods and Results-Symptomatic patients with large caliber true bifurcation lesions (SB diameter ≥2.5 mm) and significant ostial disease length (≥5 mm) were randomized to either a provisional T-stent strategy or a dual stent culotte technique. Two hundred patients aged 64±10 years, 82% male, were randomized in 20 European centers. The clinical presentations were stable coronary disease (69%) and acute coronary syndromes (31%). SB stent diameter (2.67±0.27 mm) and length (20.30±5.89 mm) confirmed the extent of SB disease. Procedural success (provisional 97%, culotte 94%) and kissing balloon inflation (provisional 95%, culotte 98%) were high. Sixteen percent of patients in the provisional group underwent T-stenting. The primary end point (a composite of death, myocardial infarction, and target vessel revascularization at 12 months) occurred in 7.7% of the provisional T-stent group versus 10.3% of the culotte group (hazard ratio, 1.02; 95% confidence interval, 0.78-1.34; P=0.53). Procedure time, X-ray dose, and cost all favored the simpler procedure. Conclusions-When treating complex coronary bifurcation lesions with large stenosed SBs, there is no difference between a provisional T-stent strategy and a systematic 2-stent culotte strategy in a composite end point of death, myocardial infarction, and target vessel revascularization at 12 months. Clinical Trial Registration-URL: http://www.clinicaltrials.gov. Unique identifier: NCT 01560455.
AB - Background-For the treatment of coronary bifurcation lesions, a provisional strategy is superior to systematic 2-stent techniques for the most bifurcation lesions. However, complex anatomies with large side branches (SBs) with significant ostial disease length are considered by expert consensus to warrant a 2-stent technique upfront. This consensus view has not been scientifically assessed. Methods and Results-Symptomatic patients with large caliber true bifurcation lesions (SB diameter ≥2.5 mm) and significant ostial disease length (≥5 mm) were randomized to either a provisional T-stent strategy or a dual stent culotte technique. Two hundred patients aged 64±10 years, 82% male, were randomized in 20 European centers. The clinical presentations were stable coronary disease (69%) and acute coronary syndromes (31%). SB stent diameter (2.67±0.27 mm) and length (20.30±5.89 mm) confirmed the extent of SB disease. Procedural success (provisional 97%, culotte 94%) and kissing balloon inflation (provisional 95%, culotte 98%) were high. Sixteen percent of patients in the provisional group underwent T-stenting. The primary end point (a composite of death, myocardial infarction, and target vessel revascularization at 12 months) occurred in 7.7% of the provisional T-stent group versus 10.3% of the culotte group (hazard ratio, 1.02; 95% confidence interval, 0.78-1.34; P=0.53). Procedure time, X-ray dose, and cost all favored the simpler procedure. Conclusions-When treating complex coronary bifurcation lesions with large stenosed SBs, there is no difference between a provisional T-stent strategy and a systematic 2-stent culotte strategy in a composite end point of death, myocardial infarction, and target vessel revascularization at 12 months. Clinical Trial Registration-URL: http://www.clinicaltrials.gov. Unique identifier: NCT 01560455.
KW - Acute coronary syndrome
KW - Cardiology and Cardiovascular Medicine
KW - confidence interval
KW - coronary disease
KW - myocardial infarction
KW - stent
KW - Acute coronary syndrome
KW - Cardiology and Cardiovascular Medicine
KW - confidence interval
KW - coronary disease
KW - myocardial infarction
KW - stent
UR - http://hdl.handle.net/10807/98689
UR - http://circinterventions.ahajournals.org/
U2 - 10.1161/CIRCINTERVENTIONS.115.003643
DO - 10.1161/CIRCINTERVENTIONS.115.003643
M3 - Article
SN - 1941-7640
VL - 9
SP - N/A-N/A
JO - CIRCULATION. CARDIOVASCULAR INTERVENTIONS.
JF - CIRCULATION. CARDIOVASCULAR INTERVENTIONS.
ER -