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不同阿司匹林起始剂量对ST段抬高心肌梗塞患者溶栓治疗的影响 被引量:2

Effect of different initial aspirin dose in ST-elevation myocardial infarction patients treated with fibrinolytic therapy
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摘要 【目的】探讨对ST段抬高的心肌梗塞(ST-elevation myocardial infarction,STEMI)患者进行溶栓治疗,应用不同起始剂量阿司匹林后的影响。【方法】我们选择了227例STEMI患者作为研究对象。我们比较了应用150 mg和300 mg阿司匹林后,24 h、7 d和30 d死亡率,和住院期间出现中-重度出血的发生率。【结果】113名患者接受首剂300 mg阿司匹林治疗,114名患者接受首剂150 mg阿司匹林治疗。300 mg组和150 mg组的24 h死亡率是3.54%vs3.51%。而7 d和30 d的死亡率分别是5.31%vs4.39%和7.08%vs6.14%(P>0.05)。300 mg组住院期间出现中-重度出血发生率是12.4%,而150 mg组是8.8%(P<0.05)。【结论】在STEMI治疗中首剂应用150 mg与300 mg阿司匹林效果相同,但安全系数前者大于后者。 [ Objective] To investigate the effect of different initial aspirin dose in ST-elevation myocardial infarction patients treated with fibrinolytic therapy. [Methods] A total of 227 ST-elevation myocardial infarction patients were selected for the study. Initial aspirin dose of 150 mg versus 300 mg was selected and 24-hour, 7-day and 30-day mortality, as well as rates of inhospital moderate/severe bleeding were cempared. [ Results] 113 patients received an initial aspirin dose of 300 mg, and 114 patients received 150 mg. The 24-hour mortality rates were 3.54% and 3.51% for those receiving an initial aspirin dose of 300 mg and 150 mg. Mortality rates at 7 and 30 days were 5.31% and 4.39% and 7.08% and 6.14% among patients receiving 300 mg and 150 mg aspirin. In-hospital moderate/severe bleeding occurred in 12.4% of those treated with 300 nag and 8.8% among those receiving 150 mg( P 〈 0.05) . [ Conclusions] The initial dose of 150 mg aspirin may be as effective as and perhaps more safe than 300 mg for the acute treatment of ST-elevation myocardial infarction.
出处 《武警医学院学报》 CAS 2009年第2期125-126,129,共3页 Acta Academiae Medicinae CPAPF
关键词 阿司匹林 死亡率 出血 心肌梗塞 Aspirin Mortality Bleeding Myocardial infarction
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  • 1Collaborative overview of randomised trials of antiplatelet therapy,Ⅰ: prevention of death, myocardial infarction, and stroke by prolonged antiplatelet therapy in various categories of patients: Antiplatelet Trialists' Collaboration[J]. BMJ, 1994,308:81 - 106.
  • 2Antithrombotic Trialists' Collaboration. Collaborative meta-analysis of randomised trials of antiplatelet therapy for prevention of death, myocardial infarction, and stroke in high risk patients [J ]. BMJ, 2002,324(7329):71 - 86.
  • 3Patrono C, Coller B, FitzGerald GA, et al. Platelet-active drugs: the relationships among dose, effectiveness, and side effects: the Seventh AC- CP Conference on Antithrombotic and Thromholytic Therapy[J]. Chest, 2004,126(3 suppl) :234 - 264.
  • 4Tickoo S, Roe MT, Peterson ED, et al. Patterns of aspirin dosing in non- ST-elevation acute coronary syndromes in the CRUSADE Quality Improvement Initiative[ J]. Am J Card iol, 2007,99 ( 11 ) : 1496 - 1499.
  • 5Campbell CL, Smyth S, Montalescot G, et al. Asirinp dose for the prevention of cardiovascular disease: a systematic review[ J]. JAMA, 2007, 297(18) :2018 - 2024.
  • 6Grosser T, Fries S, FitzGerald GA. Biological basis for the cardiovascular consequences of COX-2 inhibition: therapeutic challenges and opportunities[ J]. J Clin Invest, 2006,116( 1 ) :4 - 15.
  • 7Serebruany VL, Steinhubl SR, Berger PB, et ol. Analysis of risk of bleeding complications after different doses of aspirin in 192,036 patients enrolled in 31 randomized controlled trials[J]. Am J Cardiol, 2005, 95 (10) : 1218 - 1222.
  • 8Pedersen AK, FitzGerald GA. Dose-related kinetics of aspirin: presystemic acetylation of platelet cyclooxygenase[ J]. N Engl J Med, 1984,311(19):1206- 1211.

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