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Sarpogrelate treatment reduces restenosis after coronary stenting
被引:47
|作者:
Fujita, M
Mizuno, K
Ho, M
Tsukahara, R
Miyamoto, A
Miki, O
Ishii, K
Miwa, K
机构:
[1] Kyoto Univ, Coll Med Technol, Sakyo Ku, Kyoto 6068507, Japan
[2] Chiba Hokusah Hosp, Nippon Med Sch, Dept Internal Med, Chiba, Japan
[3] Kawasaki Social Insurance Hosp, Div Cardiol, Kanagawa, Japan
[4] Kawasaki Saiwai Hosp, Div Cardiol, Kanagawa, Japan
[5] Kansai Elect Power Hosp, Dept Internal Med 2, Osaka, Japan
关键词:
D O I:
10.1067/mhj.2003.176
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Background Sarpogrelate, a serotonin blacker, has been reported to inhibit the serotonin-induced proliferation of rat aortic smooth muscle cells. The aim of this study was to investigate whether sarpogrelate reduces restenosis after coronary stenting as a result of prevention of intimal hyperplasia. Methods We examined 79 patients with stable angina undergoing elective coronary stenting on de novo lesions of native coronary arteries in a prospective, randomized trial. All enrolled patients received aspirin and ticlopidine, and one third of the patients were assigned to receive oral sarpogrelote. Results Treatment with sarpogrelate in addition to aspirin and ticlopidine caused no major adverse cardiovascular events or hemorrhagic adverse effects during the 6-month follow-up period. The restenosis rate in the group of patients receiving sarpogrelate was 4.3%, which was significantly lower than the 28.6% rate found in the group of patients not receiving sarpogrelate. Conclusions Sarpogrelate treatment reduces restenosis after coronary stenting, which suggests that serotonin released from activated platelets may ploy an important role in stent restenosis.
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