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不稳定型心绞痛的治疗进展
http://www.100md.com 《中华现代护理学杂志》 2000年第1期
     作者:吕钰 吕新华 耿君 董丽华

    单位:山东省滨州地区医院(256610)

    关键词:

    中国综合临床000102 不稳定型心绞痛(UAP)是介于劳累性稳定型心绞痛与急性心肌梗死(AMI)和猝死之间的临床表现。主要包括①初发心绞痛,②恶化劳力性心绞痛,③静息心绞痛伴心电图缺血改变,④心肌梗死后早期心绞痛[1]。由于它具有独特的病理生理机制及临床预后,如果不能恰当及时的治疗,患者可能发展为AMI,甚至猝死,故加强对UAP治疗至关重要。近年来对UAP的治疗研究较多,综述如下。

    1药物治疗

    1.1抗血小板治疗

    1.1.1阿斯匹林阿斯匹林通过抑制环氧化酶,使血栓素A2(TXA2)的合成减少,从而抑制血栓的形成。在心肌梗死和死亡危险性研究(RISC)[2],中,UAP患者服用阿斯匹林每日75mg,结果用药5天病死率和AMI发生率从5.7%降至2.5%,危险性下降57.0%;30天时从13.3%降至4.2%;3个月时从17.0%降至6.5%。Theroux等[3]观察一组UAP急性期患者,随机给阿斯匹林和安慰剂,结果6天时阿斯匹林组AMI的发生率为2.5%,而对照组为6.4%,危险性下降63.0%。美国退伍军人管理局的研究表明阿斯匹林治疗的UAP组致命性和非致命性AMI的发生率从10.1%降至5.0%。随访1年,阿斯匹林组的病死率仍较对厢组下降43.0%(5.5%比9.5%),提示病变过程已获控制[4]。对于阿斯匹林的最佳剂量目前尚不清楚,国内推荐剂量为每日80~325mg。
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    1.1.2血小板膜糖蛋白Ⅱb/Ⅲ.(GPⅡb/Ⅲa)受体拮抗剂包括GPⅡb/Ⅲa受体单克隆抗体如C7E3,合成的肽类制剂如Intigrelin和合成的非肽类制剂如Lamifiban和噻氯吡啶(ticlopidine)等。药理作用:作用于血小板膜GPⅡb/Ⅲa受体这一血小板聚集的中心环节,从根本上抑制血小板聚集反应。一项1200例UAP患者的多个临床试验[5]综合显示,GPⅡb/Ⅲa受体拮抗剂使UAP患者心脏事件(包括冠心病死亡,非致死性AMI和顽固性心绞痛)发生率下降了40.0%~50.0%。加拿大对Lamifiban的研究[6],包括了15个中心的365例UAP患者,随机1次给予Lamifiban静脉150~750μg/kg后连续72~120小时静脉滴注1~5μg/(ks·min)加口服阿斯匹林325mg/d或仅给阿斯匹林治疗。与对照组比较,Lamifiban治疗组用药期间和1个月内冠心病死亡、非致命性AMI、紧急冠脉血管再建术均显著减少(P<0.05),非颅内和非威胁生命的出血为21.9%,对照组为0.8%。Balsano等[7]研究652例UAP患者,在人院后48小时内,随机给予噻氯吡啶250mg,2次/d或对照剂,随访6个月,噻氯吡啶使致死性和非致死性的AMI发生率从13.6%降至7.3%,危险性下降46.3%。该类药物中虽然噻氯吡啶和C7E3已在临床应用,但大规模前瞻性临床研究仍在进行,以进一步了解其剂量、疗效和安全性等关系。……
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    收稿日期:1998-09-11

    修稿日期:1999-08-18, 百拇医药