老年患者置入新型药物洗脱支架术后6个月与12个月双联抗血小板治疗的有效性和安全性比较Six versus twelve months of dual antiplatelet therapy after implantation of biodegradable polymer sirolimus-eluting stent in elderly patients
杨靖,李毅,裘淼涵,王贺阳,徐凯,荆全民,韩雅玲,李晶
摘要(Abstract):
目的比较老年患者置入新型药物洗脱支架(BP-SES)术后,应用6个月与12个月双联抗血小板治疗(DAPT)的疗效和安全性。方法纳入I-LOVE-IT 2研究中置入BP-SES老年患者(≥65岁)627例,其中接受6个月DAPT治疗319例(6个月DAPT组),12个月DAPT治疗308例(12个月DAPT组)。本研究的主要终点为12个月的靶病变失败(TLF,包含心源性死亡、靶血管心肌梗死和临床驱动的靶病变再次血运重建的复合终点),次要终点为12个月净不良临床事件(NACE,包含全因死亡、心肌梗死、缺血性卒中或全部出血的复合终点)以及12个月支架内血栓形成发生率。结果两组患者年龄、性别、体重指数、糖尿病、高血压病等方面比较,差异均无统计学意义(均P>0.05)。基线SYNTAX评分、靶病变个数、靶血管位置等基线造影特征方面比较,差异均无统计学意义(均P>0.05)。随访12个月Kaplan-Meier累积事件,6个月DAPT组主要终点TLF发生率(7.2%比7.1%,P=0.980),次要终点NACE发生率(14.1%比13.0%,P=0.726),支架内血栓形成发生率(2.8%比1.0%,P=0.101)与12个月DAPT组比较,差异均无统计学意义。明确或极可能的支架内血栓形成共5例,其中6个月和12个月DAPT组分别有3例和2例(0.9%比0.6%,P=0.682),差异无统计学意义。界标分析结果显示,在6至12个月随访期间,6个月DAPT组TLF(2.3%比1.7%,P=0.593),NACE事件发生率(4.2%比2.9%,P=0.392),出血发生率(1.0%比1.0%,P=0.961)与12个月DAPT组比较,差异无统计学意义。结论在接受新一代药物洗脱支架置入的老年患者中,术后接受6个月DAPT治疗者,有效性和安全性与接受12个月DAPT的患者差异无统计学意义。
关键词(KeyWords): 老年;双联抗血小板治疗;聚合物涂层可降解西罗莫司(雷帕霉素)药物洗脱支架
基金项目(Foundation):
作者(Author): 杨靖,李毅,裘淼涵,王贺阳,徐凯,荆全民,韩雅玲,李晶
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