南方医科大学学报 ›› 2004, Vol. 24 ›› Issue (01): 81-84.

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ST段抬高型急性心肌梗死溶栓治疗后不同抗凝治疗的临床观察

张晔, 王旭开, 杨成明, 刘光耀   

  1. 第三军医大学大坪医院心血管内科, 重庆, 400042
  • 出版日期:2004-01-20 发布日期:2004-01-20
  • 基金资助:
    收稿日期:2003-8-14。
    作者简介:张晔(1978- ),女,2000年毕业于第三军医大学,现为在读硕士研究生,医师,主要从事临床心血管内科疾病方面的研究,电话:023-68757266
    通讯作者:王旭开,男,博士,教授、主任医师,电话:023-68757266

Use of unfractionated heparin and a low-molecular-weight heparin following thrombolytic therapy for acute ST-segment elevation myocardial infarction

ZHANG Ye, WANG Xu-kai, YANG Cheng-ming   

  1. 第三军医大学大坪医院心血管内科, 重庆, 400042
  • Online:2004-01-20 Published:2004-01-20

摘要: 目的 观察比较ST段抬高型急性心肌梗死溶栓治疗后普通肝素(UFH)和parnaparin(商品名新复先) 两种不同抗凝辅助治疗方法的疗效和安全性。方法 186名入院后接受溶栓治疗的ST段抬高型急性心肌梗死患者随机分为2组,UFH组及parnaparin组。UFH组在溶栓治疗后12h给予肝素100U/kg·b.w.静脉推注,续1000U/h静脉滴注,维持活化的部分凝血活酶时间为正常对照的1.5~2.0倍,连续3d后改为皮下注射7500U每12h1次,连续注射4d。parna-parin组在溶栓治疗后12 h给予parnaparin0.4ml皮下注射,每12 h1次,连续注射7d。主要观察终点:治疗2、7、14、30 d内发生心脏性或非心脏性死亡、再梗死、药物治疗疗效差而必须行急诊血运重建的三联终点事件(死亡、心肌再梗死、紧急血运重建术)。所有入选患者住院14d以上,随访至治疗后45d。结果 随访45d内复合三联终点事件在par-naparin组明显下降(42.22% vs37.08%,P=0.03),出血事件(10.00% vs 3.13%,P=0.06)及血小板减少(3.33% vs 0,P=0.07)亦少于UFH组。结论 做为ST段抬高型急性心肌梗死溶栓治疗后的辅助抗凝治疗,parnaparin较UFH至少在45d内更能减少心脏事件的再发生,更少发生出血事件和血小板减少。

Abstract: Objective To compare the efficacy and safety of unfractionated heparin with a low -molecular-weight heparin (par-naparin) in the management of anticoagulation fol lowing thrombolytic therapy for acute ST-segment elevation myocardial in-farctio n.Methods One hundred and eighty-six patients with acute ST-segment elevation m yocardial infarction undergoing thrombolytic therapy were randomly assigned to receive either unfractionated heparin (100 U/kg·b.w. intravenous bolus, 1000U/h continuous infusion for 3 days just 12h after thrombolysis to maintain the activated partial thromboplastin time at 1.5 to 2.0 times as normal, then subcut aneous 7500U every 12h for 4 days, n=90) or parnaparin (0.4ml subcutaneously every 12h for 7 days 12h after thrombolysis, n=96) in conjunction with routi ne therapy. The patients enrolled stayed in hospital for at least 14 days and were followed for 45 days after admission into the hospital.Results The composit e triple end-point (death, recurrent myocardial infarction, emergency revascula rization assessed at 2, 7, 14, 45 days) was significantly reduced in pa-tients receiving parnaparin(42.22% vs 37.08%, P=0.03).Compared with unfractionated he parin group, the incidences of hemorrhage (10.00% vs3.13%, P=0.06)and heparin -induced thrombocytopenia (3.33% vs 0, P=0.07) were also lower in par-naparin gro up.Conclusion Parnaprin is more effective in reducing composite cardiac events, hemorrhage and heparin-in-duced thrombocytopenia at least in 45 days as compare d with unfractionated heparin during anticoagulation following throm-bolytic the rapy for acute ST-segment elevation myocardial infarction.

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