期刊文献+

PCI患者氯吡格雷抵抗与CD62p的关系研究 被引量:1

Analyze the relativity of the clopidogrel resistance and CD62p after PCI
下载PDF
导出
摘要 目的观察在经皮冠状动脉介入治疗(PCI)患者中硫酸氯吡格雷抵抗的发生情况。评价p-选择素与氯吡格雷抵抗发生率的相关性,并进一步探讨氯吡格雷抵抗与CD62p的关联性。方法 86名接受PCI治疗的患者在服用氯吡格雷前及一月后抽血,利用比浊法测定ADP诱导的血小板最大聚集率(PAGM),同时用流式细胞术测定CD62p。根据PAGM降低程度判断氯吡格雷抵抗发生率。结果 86例给予氯吡格雷300mg负荷量并行PCI患者发生氯吡格雷抵抗者为22例(25.4%)。CD62p与PAGM具有正相关。结论 PCI介入治疗的患者中存在部分氯吡格雷抵抗者。CD62p与PGAM相关,且百分比相比更具有意义。氯吡格雷抵抗可用CD62p的下降程度来界定。 Objective To observe the percutaneous coronary intervention (PCI) in patients with clopidogrel resistance happened. The purpose is to evaluate the incidence of clopidogrel resistance of the relevance, and to further explore the relevance of CD62P and clopidogrel resistance. Methods Taking the clopidogrel before and after 30days, 86 patients who receive PC] are blooded. Turbidimetry detect maximum platelet aggregation(PAGM) ,which use ADP-induced. Meanwhile, we use the flow Cytometry (FCM) to detect CD62p. According to the extent of the PAGM reducing, we judge the incidence of clopidogrel resistance. Results Clopidogrel resistance has occurred in 22 patients (25.4%) in PCI patients. CD62p and PAGM are positively correlated. Conclusion To some patients, there are clopidogrel resisters in PCI. CD62p relates with PGAM. Furthermore, percentages are more meaningful. Clopidogrel resistance can be defined by the extent of CD62p.
出处 《中国老年保健医学》 2012年第4期15-18,共4页 Chinese Journal of Geriatric Care
关键词 PCI 氯吡格雷抵抗 CD62P PCI,clopidogrel resistance,CD62p
  • 相关文献

参考文献25

  • 1yuqing Huo, Schober A, Forlow SB, et al. Circulating activated plate-lets exacerbate atheros clerosis in mice deficient in apolipoproteein E [ J ]. Nature Medicine, 2003,9:61 - 67.
  • 2Yusuf S, Zhao F, Mehta SR, et al. Effects of clopidogrel in addition to aspirin in patients with acute coronary syndromes without ST-segment elevation. The Clopidogrel in Unstable Angina to Prevent Recurrent E- vents Trial Investigators[J]. N Engl J Med ,2001,345:494 - 502.
  • 3Steinhubl SR, Berger PB, Mann JT III, et al. Early and sustained dual oral antiplatelet therapy following percutaneous coronary intervention : a randomized controlled trial. CREDO Investigators. Clopidogrel for the Reduction of Events During Observation[J]. JAMA,2002,288:2411 - 2420.
  • 4刘萍,徐建民.氯吡格雷的抗栓作用[J].中国新药与临床杂志,2001,20(5):384-386. 被引量:24
  • 5Steinhubl SR, Berger PB, Mann JT, Fry ET, Del,ago A, Wilmer C, Topoi EJ. Early and sustained dual oral antiplatelet therapy following percutaneous coronary intervention: a randomized controlled trial [ J ]. JAMA,2002,288 : 2411 - 2420.
  • 6Shlomi Matetzky, MD; oris Shenkman, M D, PhD; ictorGuetta, MD; M ichael Shechter,MD;et al, Clopidogrel Resistance Is Associated With Increased Risk of Recurrent Atherothrombotic Events in Patients With Acute Myocardial Infarction[ J]. Circulation, 2004,109:3171 - 3175.
  • 7Guthikonda S, Lev EI, Kleiman NS. Resistance to antiplatelet therapy [ J ]. Curr Cardiol Rep,2005,7 (4) :242 - 248.
  • 8Massberg S,Svchuh C. Gawaz M. Role of pahelets in the pathophysiology of acute coronary syndrome[J]. Semin Vasc Med ,2003,3 : 147 - 162.
  • 9Muller I. Besta F. Schulz C. et al. Prevalence of clopidogrel nonrespon- ders among patients with stable angina peetoris scheduled for elective coronary stent placement[J]. romb Haemost ,2003,89 ( 5 ) :783 - 784.
  • 10Paul A,Gurbel M D,et al. Clopidogrel for coronary stenting:Response varisbility,drug resistance,and the effect of pretreatment.platelet reac- tivity[ J]. Circulation ,2003,107:2908 - 2913.

二级参考文献16

  • 1陈骏,龚肖崎,张亚霏.细胞粘附分子的免疫学定量检测方法及其临床应用[J].国外医学(免疫学分册),1993,16(6):310-313. 被引量:2
  • 2[1]Feliste R, Delebassee D, Simon MF, et al. Broad spectrum anti-platelet activity of ticlopidine and PCR 4099 involves the suppression of the effects of released ADP[J]. Thromb Res, 1987, 48:403-415.
  • 3[2]Minno GD, Cerbone AM,Mattioli PL,Turco S,Iovine C, Mancini M. Fun ctionally thrombasthenic state in normal platelets following the administration of ticlopidine[J]. J Clin Invest, 1985, 75:328-330.
  • 4[3]Gachet C,Savi P,Ohlmann P,Maffrand JP,Jakobs KH, Cazenave JP. AD P receptor induced activation of guanine nucleotide binding proteins in rat plat elet membranes--an effect selectively blocked by the thienopyridine clopidogre l[J]. Throb Haemost, 1992, 68:79-83.
  • 5[4]Maffrand JP, Bernat A, Delebassee D, Defreyn G, Cazenave JP, Gordon JL. ADP plays a key role in thrombogenesis in rats[J]. Thromb haemost, 1988, 5 9:225-230.
  • 6[5]Born GVR. Adenosine diphosphate as a mediator of platelet aggregatio n in vivo: an editorial view[J]. Circulation, 1985, 72:741-746.
  • 7[6]Zawilska KM, Born GVR, Begent NA. Effect of ADP-utilizing enzymes o n the arterial bleeding time in rats and rabbits[J]. Br J Haematol, 1988, 50:3 17-319.
  • 8[7]Herbert JM, Bemat A, Mur A, Maffrand JP. Effect of aprotinin on ble ed ing occurring after administration of clopidogrel in the rat[J]. Thromb Res, 1 993, 65:S160.
  • 9[8]Shand RA, Smith JR, Wallis RB. Expression of the paltelet procoagul a nt activity in vivo in thrombus formation in an extracorporeal shunt in the rat[J]. Thromb Res, 1984, 36:223-232.
  • 10[9]Barthclemy G, Broussy R, Herbert JM, Detreyn G, Maffrand JP. Compara tive effects of clopidogrel nafagrel (DP1904). And aspirin on cyclic flow variat ions in stenosed and in jured arteries in the dog[J]. Thromb haemost, 1991,65 :1177.

共引文献46

同被引文献4

  • 1Jaremo P, LindahlT, Fransson S, etal Individual variations of platelet- inh ib ition after load ing doses of elopidogrel[ J]. J Intern Med ,2002, 252 : 233 - 238.
  • 2GurbelP, Bliden K, HiattB, etal Clopido grel for coronary stenting: re- sponse variab ility, drug resistance, and the effect of pretreatm entp latelet reactivity [J]. Circu lation,2003 ,107 :2908 -2913.
  • 3M uller I, BestaF, Schulz C, etal Prevallence of C lopidogrel nonrepon- dersam ong patients w ith tab leangina pectoris schedu led for elective coronary steng placement [ J ] . Thromb Haemost, 2003,89:783 - 787.
  • 4赵秀丽,胡大一.氯吡格雷[J].临床药物治疗杂志,2003,1(1):61-61. 被引量:8

引证文献1

二级引证文献1

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