TY - JOUR
T1 - Dual antiplatelet therapy duration and clinical outcomes following treatment with zotarolimus-eluting stents
AU - Kandzari, David E.
AU - Barker, Colin S.
AU - Leon, Martin B.
AU - Mauri, Laura
AU - Wijns, William
AU - Fajadet, Jean
AU - Mehran, Roxana
N1 - Funding Information:
Dr. Kandzari has received consulting honoraria and research/grant support from Medtronic and Abbott Vascular ; and is on the advisory board for Medtronic. Dr. Barker is on the Speakers’ Bureau of and has received honoraria from Cordis, Medtronic, and Abbott Cardiovascular. Dr. Leon has received research grant support from and is on the advisory board for Medtronic . Dr. Mauri has received grants (to her institution) from Abbott , Boston Scientific , Medtronic , Cordis , Bristol-Myers Squibb , Sanofi-Aventis , Eli Lilly , and Daiichi Sankyo ; and is a consultant for Abbott, Medtronic, and Cordis. Any grants, research contracts, fees, or honoraria on behalf of Dr. Wijns go to the Cardiovascular Research Center, Aalst, Belgium. Dr. Fajadet has reported that she has no relationships relevant to the contents of this paper to disclose. Dr. Mehran is a consultant for Abbott Vascular, AstraZeneca, Medtronic, and Regado Biosciences; and has received research support from Medtronic and BMS/Sanofi-Aventis.
PY - 2011/10
Y1 - 2011/10
N2 - Objectives: We sought to evaluate differences in late safety outcomes relative to dual antiplatelet therapy (DAPT) duration in patients treated with zotarolimus-eluting stents (ZES). Background: Despite treatment recommendations for at least 12 months of DAPT following drug-eluting stent revascularization, device-specific outcomes relative to DAPT duration are absent. Methods: Among 2,032 patients undergoing percutaneous coronary revascularization with ZES in 5 trials, late safety events were compared relative to DAPT duration for patients with <6 months DAPT adherence and survival free of major ischemic and bleeding events. Results: A total of 1,414 event-free patients on DAPT at 6 months were identified. Patient group comparisons relative to DAPT included: 6 months versus <12 months, and 6 months versus ≥24 months. Through 3 years, risk-adjusted ischemic event rates did not significantly differ between groups: 6 versus ≥12 months: death (2.7% vs. 2.2%), myocardial infarction (MI, 0.3% vs. 1.1%), and definite/probable stent thrombosis (ST, 0.3% vs. 0%); 6 versus ≥24 months: death (1.6% vs. 1.6%), MI (0.4% vs. 1.2%), and definite/probable ST (0.1% vs. 0.2%). Composite events also did not statistically vary between DAPT durations. In multivariable analysis, 6-month versus longer DAPT duration was not associated with increased likelihood of thrombotic events at 3-year follow-up. Major bleeding was negligible across groups. Conclusions: Among patients treated with ZES, late-term events of death, MI, stroke, and ST do not significantly differ between patients taking 6 months DAPT compared with continuation beyond 1 year. These findings merit further study to identify the appropriate duration of DAPT according to specific drug-eluting stents.
AB - Objectives: We sought to evaluate differences in late safety outcomes relative to dual antiplatelet therapy (DAPT) duration in patients treated with zotarolimus-eluting stents (ZES). Background: Despite treatment recommendations for at least 12 months of DAPT following drug-eluting stent revascularization, device-specific outcomes relative to DAPT duration are absent. Methods: Among 2,032 patients undergoing percutaneous coronary revascularization with ZES in 5 trials, late safety events were compared relative to DAPT duration for patients with <6 months DAPT adherence and survival free of major ischemic and bleeding events. Results: A total of 1,414 event-free patients on DAPT at 6 months were identified. Patient group comparisons relative to DAPT included: 6 months versus <12 months, and 6 months versus ≥24 months. Through 3 years, risk-adjusted ischemic event rates did not significantly differ between groups: 6 versus ≥12 months: death (2.7% vs. 2.2%), myocardial infarction (MI, 0.3% vs. 1.1%), and definite/probable stent thrombosis (ST, 0.3% vs. 0%); 6 versus ≥24 months: death (1.6% vs. 1.6%), MI (0.4% vs. 1.2%), and definite/probable ST (0.1% vs. 0.2%). Composite events also did not statistically vary between DAPT durations. In multivariable analysis, 6-month versus longer DAPT duration was not associated with increased likelihood of thrombotic events at 3-year follow-up. Major bleeding was negligible across groups. Conclusions: Among patients treated with ZES, late-term events of death, MI, stroke, and ST do not significantly differ between patients taking 6 months DAPT compared with continuation beyond 1 year. These findings merit further study to identify the appropriate duration of DAPT according to specific drug-eluting stents.
KW - antiplatelet therapy
KW - drug-eluting stent(s)
KW - stent thrombosis
KW - zotarolimus-eluting stent(s)
UR - http://www.scopus.com/inward/record.url?scp=80054972182&partnerID=8YFLogxK
U2 - 10.1016/j.jcin.2011.06.017
DO - 10.1016/j.jcin.2011.06.017
M3 - Article
C2 - 22017938
AN - SCOPUS:80054972182
SN - 1936-8798
VL - 4
SP - 1119
EP - 1128
JO - JACC: Cardiovascular Interventions
JF - JACC: Cardiovascular Interventions
IS - 10
ER -