摘要
目的对西罗莫司洗脱支架(SES)和其他冠脉支架治疗冠心病的临床安全性进行比较。方法通过文献检索国内外大型数据库如pubmed、OVID medline、sciencedirect、CNKI、万方数据库等,检索近5年发表的关于SES与裸金属支架及其他药物洗脱支架术后主要心脏不良事件(MACE)、靶血管重建率和靶病变重建率等终点的对比性研究。结果SES与裸金属支架相比,术后MACE明显下降,靶血管重建率和靶病变重建率也显著下降。SES与其他药物洗脱支架相比,临床安全性与紫杉醇洗脱支架(PES)相当,在某些患者(如合并糖尿病或冠脉分叉病变)可能优于佐他莫司洗脱支架(ZES)。对于合并肾功能不全的患者,SES同样优于BES,安全性与PES相当。C反应蛋白对于SES术后发生MACE可能具有预测价值。结论 SES与裸金属支架相比,安全性明显提高,与PES相当。
Objective To compare the clinical safety of sirolimus-eluting stent(SES) and other coronary stents in treating coronary artery disease. Methods All comparision study relating to the endpoints of SES in treating coronary artery disease published in the last five years, including major adverse cardiac events(MACE), target vessel revascular- ization(TVR), target lesion revascularization(TLR.), are retrieved by indexing pubmed, OVID medline,sciencedirect, CNKI and Wanfang Data. Results Compared to bare-metal stent(BMS), the MACE of SES decreased obviously, at the same time TVR and TLIL of SES dropped in significantly too. Contrasting to other drug-eluting stents, the clinical safety of SES was equal to PES, and better than ZES in some patients who had complications of diabetes mellitus or coronary bifurcation lesions. For patients with renal inadequacy, the clinical safety of SES was better than BMS and equal to PES. Perhaps C-reactive protein had a predictive value of the MACE incidence after SES implantation. Conclusion Compared to BMS, SES preferred to show a significantly higher safety which equals to PES.
出处
《中国药物警戒》
2012年第6期363-366,共4页
Chinese Journal of Pharmacovigilance
关键词
西罗莫司洗脱支架
裸金属支架
紫杉醇洗脱支架
佐他莫司洗脱支架
主要心脏不良事件
靶血管重建率
靶病变重建率
sirolimus-eluting stent
bare-metal stent
pachtaxel-eluting stent
zotarolimus-eluting stents
major adverse cardiac events
target vessel revascularization
target lesion revascularization