Bhatt D L, Topol E J
Department of Cardiology, F25, Cleveland Clinic Foundation, 9500 Euclid Ave, Cleveland, OH 44195, USA.
JAMA. 2000 Sep 27;284(12):1549-58. doi: 10.1001/jama.284.12.1549.
The central role of platelet-rich thrombus in the pathogenesis of acute coronary syndromes (ACSs) is well-known. Glycoprotein IIb/IIIa (Gp IIb/IIIa) receptor antagonists are potent inhibitors of platelet function that may be expected to affect favorably the natural history of ACSs.
To define the optimal role of Gp IIb/IIIa inhibitors in treatment strategies for ACSs.
A MEDLINE search was performed to identify all English-language articles regarding use of Gp IIb/IIIa inhibitors in ACSs published between 1966 and June 2000. In addition, relevant abstracts from the annual meetings of the American Heart Association, American College of Cardiology, and the European Society of Cardiology were reviewed.
Only studies of 500 or more patients were included. Of 15 studies identified, 10 randomized, placebo-controlled, double-blind trials of Gp IIb/IIIa inhibitors in ACSs were selected for review.
Data quality was determined by publication in the peer-reviewed literature or presentation at an official cardiology society-sponsored meeting, as well as by verification with the primary author.
Three members of this class of drugs are available for intravenous use. Abciximab, eptifibatide, and tirofiban hydrochloride, each have data demonstrating their value in improving the outcomes of patients presenting with ACSs. Current evidence supports use of these drugs in both conservative and invasive treatment strategies. Glycoprotein IIb/IIIa-blocking therapy is safe, and with proper precautions, bleeding risks can be minimized. Biological differences exist among these agents, but as of yet, no head-to-head comparisons have been made of their clinical efficacy. Unlike intravenous Gp IIb/IIIa inhibitors, available data regarding any role of oral Gp IIb/IIIa inhibitors are not favorable.
Current data indicate that intravenous Gp IIb/IIIa inhibitor therapy merits a prominent role in the initial management of patients with ACSs. JAMA. 2000;284:1549-1558.
富含血小板的血栓在急性冠状动脉综合征(ACS)发病机制中的核心作用已广为人知。糖蛋白IIb/IIIa(Gp IIb/IIIa)受体拮抗剂是血小板功能的强效抑制剂,有望对ACS的自然病程产生有利影响。
明确Gp IIb/IIIa抑制剂在ACS治疗策略中的最佳作用。
进行了MEDLINE检索,以识别1966年至2000年6月间发表的所有关于Gp IIb/IIIa抑制剂在ACS中应用的英文文章。此外,还查阅了美国心脏协会、美国心脏病学会和欧洲心脏病学会年会的相关摘要。
仅纳入500例及以上患者的研究。在识别出的15项研究中,选择了10项关于Gp IIb/IIIa抑制剂在ACS中的随机、安慰剂对照、双盲试验进行综述。
数据质量通过在同行评审文献中的发表或在官方心脏病学会主办会议上的报告来确定,并与第一作者进行核实。
这类药物中有三种可供静脉使用。阿昔单抗、依替巴肽和盐酸替罗非班,每种都有数据证明其在改善ACS患者预后方面的价值。目前的证据支持在保守和侵入性治疗策略中使用这些药物。Gp IIb/IIIa阻断疗法是安全的,采取适当预防措施可将出血风险降至最低。这些药物之间存在生物学差异,但截至目前,尚未对它们的临床疗效进行直接比较。与静脉Gp IIb/IIIa抑制剂不同,关于口服Gp IIb/IIIa抑制剂的任何作用的现有数据并不乐观。
目前的数据表明,静脉Gp IIb/IIIa抑制剂疗法在ACS患者的初始管理中应发挥重要作用。《美国医学会杂志》。2000年;284:1549 - 1558。