临床荟萃 ›› 2021, Vol. 36 ›› Issue (11): 965-971.doi: 10.3969/j.issn.1004-583X.2021.11.001

• 循证研究 •    下一篇

半剂量与标准剂量替罗非班对中国老年急性冠状动脉综合征患者介入治疗的疗效及安全性分析:一项Meta分析

刘远良, 李彪, 蒋作锋, 主有峰, 张少衡, 王亚蓉, 李荣森, 李丽()   

  1. 暨南大学附属广州红十字会医院 心血管内科,广东 广州 510220
  • 收稿日期:2021-04-14 出版日期:2021-11-20 发布日期:2021-12-01
  • 通讯作者: 李丽 E-mail:lilygs@126.com

Efficacy and safety of half-dose versus standard-dose of tirofiban for percutaneous coronary intervention in elderly Chinese patients with acute coronary syndrome: a meta-analysis

Liu Yuanliang, Li Biao, Jiang Zuofeng, Zhu Youfeng, Zhang Shaoheng, Wang Yarong, Li Rongseng, Li Li()   

  1. Department of Cardiology, Guangzhou Red Cross Hospital Affiliated to Jinan University, Guangzhou 510220, China
  • Received:2021-04-14 Online:2021-11-20 Published:2021-12-01
  • Contact: Li Li E-mail:lilygs@126.com

摘要:

目的 系统评价半剂量与标准剂量替罗非班对中国老年急性冠状动脉综合征(ACS)患者介入治疗的疗效及安全性。 方法 计算机检索Cochrane、PubMed、Embase、万方、CNKI至2021年1月国内外公开发表的应用标准剂量与半剂量替罗非班治疗我国老年行介入治疗的ACS患者的随机对照试验研究,根据文献检验结果行meta分析,并评价发表性偏倚。结果 共检索出768篇文献,最终共纳入5篇文献,患者596例,其中半剂量组300例,标准剂量组296例。Meta分析显示:(1)疗效方面:在术后心肌梗死溶栓治疗(Thrombolysis myocardial infarction, TIMI)前向血流3级及临床主要心血管不良事件(MACE)发生率,半剂量组与标准剂量组差异均无统计学意义(P>0.05)。(2)安全性方面:半剂量组临床出血事件低于标准剂量组,差异有统计学意义[RR=3.70,95%CI=(1.89,5.00),P<0.01]。半剂量组与标准剂量组血小板减少症发生率差异无统计学意义(P=0.61)。 结论 对于中国老年ACS且行介入治疗患者而言,在常规双抗基础上,半剂量替罗非班安全性可能优于标准剂量替罗非班,二者疗效相当。

关键词: 急性冠状动脉综合征, 老年, 替罗非班, 随机对照试验, meta分析

Abstract:

Objective To systematically review the effectiveness and safety of half-dose versus standard-dose of tirofiban for percutaneous coronary intervention (PCI) in elderly Chinese patients with acute coronary syndrome (ACS).Methods Randomized controlled trials(RCTs), which were about standard or half dose of tirofiban for elderly Chinese patients with ACS undergoing PCI, and published by Cochrane, PubMed, Embase, Wanfang, and CNKI databases until January 2021 at home and abroad, were retrieved. Secondly, meta-analysis was performed based on the literature review results, and publication bias was evaluated. Results Five articles were included out of 768 retrieved literatures, a total of 596 patients were enrolled, including 300 cases in the half-dose group and 296 cases in the standard-dose group. Meta-analysis showed that, the first, in terms of curative outcomes, there was no statistically significant difference in the incidences of grade III forward-flow of postoperative thrombolysis myocardial infarction (TIMI) and major adverse cardiovascular events(MACE) in clinical between groups (P>0.05). The second, in terms of safety, the incidence of clinical bleeding downregulated notably in half-dose group when compared with standard-dose group, and with statistically significant difference [RR=3.70, 95%CI=(1.89, 5.00), P<0.01]. The difference was not statistically significant in the incidence of thrombocytopenia between groups (P=0.61).Conclusion For elderly Chinese patients with ACS undergoing PCI, on the basis of conventional double antibodies, the safety of half-dose of tirofiban might be better than that of standard-dose, and the efficacy of two doses was equivalent.

Key words: acute coronary syndrome, aged, tirofiban, randomized controlled trial, meta-analysis

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