期刊文献+

对氯吡格雷低反应的STEMI患者应用替格瑞洛后ADP诱导的血小板抑制率的变化 被引量:4

Change in platelet inhibition rate induced by ADP in STEMI patients with low response to clopidogrel after taking ticagrelor
在线阅读 下载PDF
导出
摘要 目的 探讨对氯吡格雷低反应的急性ST段抬高心肌梗死(ST segment elevation myocardial infarction,STEMI)患者应用替格瑞洛后腺苷二磷酸(adenosine diphosphate,ADP)诱导的血小板抑制率的变化。方法 连续入选2013年2月至2014年3月在复兴医院心脏中心住院,诊断为STEMI同时存在对氯吡格雷低反应性的18岁~80岁的患者共38例。将患者(在SAS软件下)随机分为替格瑞洛治疗组和常规治疗组。两组均于1周后复查ADP诱导的血小板抑制率。比较两组ADP诱导的血小板抑制率和ADP达标率。结果 与常规治疗组相比,替格瑞洛组ADP诱导的血小板抑制率明显升高,差异有统计学意义(78.32%±12.95%vs.31.89%±11.28%,t=11.779,P〈0.001]。替格瑞洛组较常规治疗组ADP达标率明显提高,差异有统计学意义[89.5%(12/19)vs.10.5%(2/19),χ2=23.684,P〈0.001)。结论 对氯吡格雷低反应的STEMI患者应用替格瑞洛后ADP诱导的血小板抑制率明显升高。 Objectives To investigate the change in platelet inhibition rate induced by adenosine diphosphate(ADP) in ST segment elevation myocardial infarction(STEMI) patients with low response to clopidogrel after taking ticagrelor.Methods We continuously selected 38 STEMI patients with low response to clopidogrel hydrogen sulfate aged from 18 to 80 years old in the Heart Center of Fuxing Hospital from February 2013 to March 2014. All the patients were randomly divided into ticagrelor treatment group and routine group. Platelet inhibition rate induced by ADP of the two groups were counterchecked in one week. Platelet inhibition rate induced by ADP and control rate of ADP between the two groups were compared. Results Compared with routine group,platelet inhibition rate induced by ADP in ticagrelor group increased significantly(78.32% ±12.95% vs. 31.89% ±11.28%, t =11.779, P〈0.001). Control rate of ADP in ticagrelor group obviously improved [89.5%(12 / 19) vs. 10.5%(2 / 19), χ2=23.684, P〈0.001]. Conclusions Platelet inhibition rate induced by ADP in STEMI patients with low response to clopidogrel significantly increases after taking ticagrelor.
出处 《岭南心血管病杂志》 2015年第2期149-151,175,共4页 South China Journal of Cardiovascular Diseases
关键词 心肌梗死 血小板聚集率 腺苷二磷酸 氯吡格雷低反应 myocardial infarction platelet aggregation rate adenosine diphosphate low response to clopidogrel
  • 相关文献

参考文献17

  • 1World Health Organiaztion. Top ten causes of death. Geneva : World Health Organization ; 2011. Available from : Http :/! www .who .int/medlacentre/factsheets/fs310_2008 .pdf. Accessed December 12, 2012.
  • 2Task Force on the management of ST-segment elevation acute myocardial infarction of the European Society of Cardiology (ESC), STEG P G, JAMES S K, et al. ESC Guidelines for the management of acute myocardial infarction in patients presenting with ST-segment elevation [J]. Eur Heart J, 2012, 33 (2) : 2569-2619.
  • 3GURBEL P A, BLIDEN K P, HIATI? B L, et al. Clopidogrel for coronary stenting: response variability, drug resistance, and the effect of pretreatment platelet reactivity [J ]. Circulation, 2003, 107(23) : 2908-2913.
  • 4DUPONT A G, GABRIEL D A, COHEN M G. Antiplatelet therapies and the role of antiplatelet resistance in acute coronary syndrome[J]. Thromb Res, 2009, 124(1): 6-13.
  • 5WALLENTIN L, BECKER R C, BUDAJ A, et al. Ticagrelor versus clopidogrel in patients with acute coronary syndromes [J]. N Engl J Med, 2009, 361(11): 1045-1057.
  • 6LOMBO B, DIEZ J G. Ticagrelor: the evidence for its clinical potential as an oral antiplatelet treatment for the reduction of major adverse cardiac events in patients with acute coronary syndromes [ J ]. Core Evid, 2011, 6 ( 1 ) : 31-42.
  • 7GURBEL P A, BLIDEN K P, BUTLER K, et al. Response to ticagrelor in clopidogrel nonrespouders and responders and effect of switching therapies the RESPOND Study [J]. Circulation, 2010, 121(10): 1188-1199.
  • 8GEISLER T, LANGER H, WYDYMUS M, et al. Low response to clopidogrel is associated with cardiovascular outcome after coronary stem implantation[J]. Eur heart J, 2006, 27(20) : 2420-2425.
  • 9LEV E I, PATEL R T, MARESH K J. Aspirin and clopidogrel drug response in patients undergoing percutaneous coronary intervention: the ole of dual drug resistance [J]. J Am Coil Cardiol. 2006. 47 (1): 27-33.
  • 10梁茜,杨希立,张健瑜,杨光,崔金环,肖平.CYP2C19基因多态性与氯吡格雷治疗后心血管事件发生!关系的研究[J].实用医学杂志,2013,29(23):3883-3884. 被引量:10

二级参考文献5

  • 1Sawada T, Shinke T, Shite J, et al. Impact of cytochrome P450 2C19 * 2 polymorphism on intra-stent thrombus after drug-eluting stent implantation in Japanese patients receiving clopidogrel [Jl. Circ J, 2011,75( 1 ) :99-105.
  • 2Fefer P, Matetzky G. The genetic basis of platelet responsiveness to clopidogrel. A critical review of the literature [J]. Thromb Haemost, 2011,106(2) : 203-210.
  • 3Bouman H J, Harmsze A M, van Werkum J W, et al. Variability in on-treatment platelet reactivity explained by CYP2C19 2 genotype is modest in clopidogrel pretreated patients undergoing coronary stenting [J]. Heart, 2011,97(15) : 1239-1244.
  • 4Hwang S J, Jeong Y H, Kim I S, et al. The eytochrome 2C19 * 2 and * 3 alleles attenuate response to clopidogrel similarly in East Asian patients undergoing elective percutaneous coronary intervention [ J ]. Thromb Res, 2011,127 ( 1 ) : 23-28.
  • 5Jang J S, Cho K I, Jin H Y, et al. Meta-analysis of cytochrome P450 2C19 polymorphism and risk of adverse clinical outcomes among coronary artery disease patients of different ethnic groups treated with elopidogrel [J]. Am J Cardiol, 2012,110(4) :502- 508.

共引文献9

同被引文献24

引证文献4

二级引证文献28

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部