TY - JOUR
T1 - Effect of Increasing Stent Length on 3-Year Clinical Outcomes in Women Undergoing Percutaneous Coronary Intervention With New-Generation Drug-Eluting Stents
T2 - Patient-Level Pooled Analysis of Randomized Trials From the WIN-DES Initiative
AU - Chandrasekhar, Jaya
AU - Baber, Usman
AU - Sartori, Samantha
AU - Stefanini, Giulio G.
AU - Sarin, Michele
AU - Vogel, Birgit
AU - Farhan, Serdar
AU - Camenzind, Edoardo
AU - Leon, Martin B.
AU - Stone, Gregg W.
AU - Serruys, Patrick W.
AU - Wijns, William
AU - Steg, Philippe G.
AU - Weisz, Giora
AU - Chieffo, Alaide
AU - Kastrati, Adnan
AU - Windecker, Stephan
AU - Morice, Marie Claude
AU - Smits, Pieter C.
AU - von Birgelen, Clemens
AU - Mikhail, Ghada W.
AU - Itchhaporia, Dipti
AU - Mehta, Laxmi
AU - Kim, Hyo Soo
AU - Valgimigli, Marco
AU - Jeger, Raban V.
AU - Kimura, Takeshi
AU - Galatius, Søren
AU - Kandzari, David
AU - Dangas, George
AU - Mehran, Roxana
N1 - Publisher Copyright:
© 2018
PY - 2018/1/8
Y1 - 2018/1/8
N2 - Objectives The aim of this study was to examine whether stent length per patient and stent length per lesion are negative markers for 3-year outcomes in women following percutaneous coronary intervention (PCI) with new-generation drug-eluting stents (DES). Background In the era of advanced stent technologies, whether stent length remains a correlate of adverse outcomes is unclear. Methods Women treated with new-generation DES in 14 randomized trials from the WIN-DES (Women in Innovation and Drug-Eluting Stents) pooled database were evaluated. Total stent length per patient, which was available in 5,403 women (quartile 1, 8 to 18 mm; quartile 2, 18 to 24 mm; quartile 3, 24 to 36 mm; quartile 4, ≥36 mm), and stent length per lesion, which was available in 5,232 women (quartile 1, 8 to 18 mm; quartile 2, 18 to 20 mm; quartile 3, 20 to 27 mm; quartile 4, ≥27 mm) were analyzed in quartiles. The primary endpoint was 3-year major adverse cardiovascular events (MACE), defined as a composite of all-cause death, myocardial infarction, or target lesion revascularization. Results In the per-patient analysis, a stepwise increase was observed with increasing stent length in the adjusted risk for 3-year MACE (p for trend <0.0001), myocardial infarction (p for trend <0.001), cardiac death (p for trend = 0.038), and target lesion revascularization (p for trend = 0.011) but not definite or probable stent thrombosis (p for trend = 0.673). In the per-lesion analysis, an increase was observed in the adjusted risk for 3-year MACE (p for trend = 0.002) and myocardial infarction (p for trend <0.0001) but not other individual endpoints. On landmark analysis for late event rates between 1 and 3 years, stent length per patient demonstrated weak associations with target lesion revascularization (p = 0.0131) and MACE (p = 0.0499), whereas stent length per lesion was not associated with higher risk for any late events, suggesting that risk was established early within the first year after PCI. Conclusions In this pooled analysis of women undergoing PCI with new-generation DES, increasing stent length per patient and per lesion were independent predictors of 3-year MACE but were not associated with definite or probable stent thrombosis.
AB - Objectives The aim of this study was to examine whether stent length per patient and stent length per lesion are negative markers for 3-year outcomes in women following percutaneous coronary intervention (PCI) with new-generation drug-eluting stents (DES). Background In the era of advanced stent technologies, whether stent length remains a correlate of adverse outcomes is unclear. Methods Women treated with new-generation DES in 14 randomized trials from the WIN-DES (Women in Innovation and Drug-Eluting Stents) pooled database were evaluated. Total stent length per patient, which was available in 5,403 women (quartile 1, 8 to 18 mm; quartile 2, 18 to 24 mm; quartile 3, 24 to 36 mm; quartile 4, ≥36 mm), and stent length per lesion, which was available in 5,232 women (quartile 1, 8 to 18 mm; quartile 2, 18 to 20 mm; quartile 3, 20 to 27 mm; quartile 4, ≥27 mm) were analyzed in quartiles. The primary endpoint was 3-year major adverse cardiovascular events (MACE), defined as a composite of all-cause death, myocardial infarction, or target lesion revascularization. Results In the per-patient analysis, a stepwise increase was observed with increasing stent length in the adjusted risk for 3-year MACE (p for trend <0.0001), myocardial infarction (p for trend <0.001), cardiac death (p for trend = 0.038), and target lesion revascularization (p for trend = 0.011) but not definite or probable stent thrombosis (p for trend = 0.673). In the per-lesion analysis, an increase was observed in the adjusted risk for 3-year MACE (p for trend = 0.002) and myocardial infarction (p for trend <0.0001) but not other individual endpoints. On landmark analysis for late event rates between 1 and 3 years, stent length per patient demonstrated weak associations with target lesion revascularization (p = 0.0131) and MACE (p = 0.0499), whereas stent length per lesion was not associated with higher risk for any late events, suggesting that risk was established early within the first year after PCI. Conclusions In this pooled analysis of women undergoing PCI with new-generation DES, increasing stent length per patient and per lesion were independent predictors of 3-year MACE but were not associated with definite or probable stent thrombosis.
KW - new-generation drug-eluting stents
KW - patient-level pooled analysis of women
KW - percutaneous coronary intervention
KW - stent length per lesion
KW - stent length per patient
UR - http://www.scopus.com/inward/record.url?scp=85039959314&partnerID=8YFLogxK
U2 - 10.1016/j.jcin.2017.11.020
DO - 10.1016/j.jcin.2017.11.020
M3 - Article
C2 - 29301648
AN - SCOPUS:85039959314
SN - 1936-8798
VL - 11
SP - 53
EP - 65
JO - JACC: Cardiovascular Interventions
JF - JACC: Cardiovascular Interventions
IS - 1
ER -