Antiplatelet therapy and long-term clinical outcome after sirolimus-eluting stent implantation: 5-year outcome of the j-Cypher registry

Due to serious concerns on very late stent thrombosis (VLST), extended use of dual antiplatelet therapy (DAPT) beyond 1 year after DES implantation has become a common clinical practice despite apparent lack of evidence suggesting its efficacy in reducing VLST. The study population consisted of 1281...

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Veröffentlicht in:Cardiovascular intervention and therapeutics 2012-09, Vol.27 (3), p.181-188
Hauptverfasser: Kimura, Takeshi, Morimoto, Takeshi, Nakagawa, Yoshihisa, Kadota, Kazushige, Nozaki, Yoichi, Tada, Tomohisa, Take, Shunsuke, Shirota, Kinya, Ito, Akira, Nakashima, Hitoshi, Fujita, Hiroshi, Kawasaki, Tomohiro, Inada, Tsukasa, Nakao, Koichi, Miyazaki, Shunichi, Doi, Osamu, Isshiki, Takaaki, Nobuyoshi, Masakiyo, Mitudo, Kazuaki
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Sprache:eng
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Zusammenfassung:Due to serious concerns on very late stent thrombosis (VLST), extended use of dual antiplatelet therapy (DAPT) beyond 1 year after DES implantation has become a common clinical practice despite apparent lack of evidence suggesting its efficacy in reducing VLST. The study population consisted of 12812 patients in the j-Cypher registry who were treated with at least one sirolimus-eluting stent (SES). We assessed the relation between duration of thienopyridine therapy and clinical outcomes with a landmark analysis at 1 year after SES implantation. Among 11713 patients without myocardial infarction (MI), stent thrombosis and stroke at 1 year who were eligible for the landmark analysis, 7414 patients (63 %) were maintained on thienopyridine at 1-year landmark point, while 4299 patients (37 %) had discontinued thienopyridine before 1-year landmark point. Patients in the on-thienopyridine group had more complex characteristics than patients in the off-thienopyridine group. Cumulative incidence of and the risk for definite VLST in the on-thienopyridine group relative to the off-thienopyridine group favored prolonged DAPT, but were not significant [0.9 and 1.2 %, P  = 0.1, and adjusted HR (95 % CI): 0.71 (0.47–1.06), P  = 0.11]. Cumulative incidence of and the risk for a composite of death, MI, or stroke in the on-thienopyridine group relative to the off-thienopyridine group were also not significant [15.3 and 14.3 %, P  = 0.15, and adjusted HR (95 % CI): 0.99 (0.89–1.11), P  = 0.89]. Prolonged use of thienopyridine beyond 1 year after SES implantation was not associated with significant decrease in the risks for VLST or for serious cardiovascular events including death, MI or stroke.
ISSN:1868-4300
1868-4297
DOI:10.1007/s12928-012-0109-0