房间隔缺损封堵术后不同抗凝方案安全性及疗效分析Safety and Efficacy of Different Anticoagulant Protocols after Transcatheter Closure of Atrial Septal Defect
张志宏,覃军,黄岚,李隆贵,宋耀明,耿召华,高凌云,林春梅,陶春蓉
摘要(Abstract):
目的评价房间隔缺损封堵术后不同抗凝方案的安全性及疗效。方法 56例房间隔缺损患者分入三组并于封堵术后给予不同抗凝方案:即肝素组(16例)持续静滴肝素钠10U.kg-1.h-1、共24h;低分子肝素组(20例)腹壁皮下注射依诺肝素1mg/kg、每12h1次,共2次和延长低分子肝素组(20例)依诺肝素用法用量同低分子肝素组、但术后连续使用3天,共6次。三组均于封堵术前2天起口服阿司匹林3mg·kg-1.d-1,至术后6个月。封堵术后三组均临床随访3个月,并于术后第30、90天复查经胸心脏超声;术后第4天测定活化部分凝血活酶时间(APTT);术后第4、7、30和90天测定血浆β-血小板球蛋白(β-TG)、血小板第4因子(PF4)和凝血酶原片段1+2(F1+2)浓度。结果 (1)封堵术后三组均无封堵器血栓形成和严重出血并发症,术后第4天三组APTT均在正常参考值范围内;(2)术前三组间β-TG、PF4和F1+2浓度差异均无统计学意义(P>0.05)。术后第4天,低分子肝素组β-TG、PF4和F1+2浓度与肝素组相比差异均无统计学意义(P>0.05),延长低分子肝素组β-TG浓度较肝素组低16%(P<0.05)、与低分子肝素组相比差异无统计学意义(P>0.05),PF4浓度较肝素组和低分子肝素组差异均无统计学意义(P>0.05),F1+2浓度较肝素组低8%(P=0.018)、较低分子肝素组低11%(P=0.035);(3)术后第7、30和90天,三组间β-TG、PF4和F1+2浓度差异均无统计学意义(P>0.05)。结论与肝素相比,低分子肝素用于房间隔缺损封堵术后抗凝两者安全性及疗效相当,延长低分子肝素疗程至术后第3天有利于降低房间隔缺损封堵术后血栓形成风险,且不增加出血风险。
关键词(KeyWords): 房间隔缺损;封堵;抗凝;肝素;肝素,低分子量
基金项目(Foundation): 重庆市重点攻关课题(cstc,2009AB5033)
作者(Author): 张志宏,覃军,黄岚,李隆贵,宋耀明,耿召华,高凌云,林春梅,陶春蓉
参考文献(References):
- [1]Du ZD,Hijazi ZM,Kleinman CS,et al.Comparison between transcatheter and surgical closure of secundum atrial septal defect in children and adults.Results of a multicenter nonrandomized trial.J Am Coll Cardiol,2002,39:1836-1844.
- [2]Acar P,Aggoun Y,Abdel-Massih T,et al.Thrombus after tran-scatheter closure of ASD with an Amplatzer septal occluder as-sessed by three dimensional echocardiographic reconstruction.Heart,2002,88:52-54.
- [3]邓东安,朱鲜阳,侯传举,等.房间隔缺损介入治疗后随诊观察.中国介入影像与治疗学,2006,5:337-340.
- [4]中华儿科杂志编辑委员会,中华医学杂志英文版编辑委员会.先天性心脏病经导管介入治疗指南.中华儿科杂志,2004,423:234-239.
- [5]秦永文.实用先天性心脏病介入治疗.上海:上海科学技术出版社,2005:31-32.
- [6]孔祥清.先天性心脏病介入治疗.南京:江苏科学技术出版社,2003:128.
- [7]李田昌,胡大一,边红,等.Amplatzer房间隔封堵治疗房间隔缺损.中国医药导刋,2003,5:182-184.
- [8]Kannan BR,Francis E,Sivakumar K,et al.Transcatheter clo-sure of very large(>or=25mm)atrial septaldefects using the Amplatzer septal occluder.Catheter Cardiovasc Interv,2003,59:522527.
- [9]Rao AK,Pratt C,Berke A,et al.Thrombolysis in Myocardial Infarction(TIMI)Trial phase I:hemorrhagic manifestations and changes in plasma fibrinogen and the fibrinolytic system in pa-tients treated with recombinant tissue plasminogen activator and streptokinase.J Am Coll Cardiol,1998,11:1-11.
- [10]胡大一,王显.房间隔部位介入治疗的焦点与思考.中国循证心血管医学杂志,2009,1(2):65-67.
- [11]Monagle P,Chalmers E,Chan A,et al.Antithrombotic therapy in neonates and children:American College of Chest Physicians Evidence-Based Clinical Practice Guidelines(8th Edition).Chest,2008,1336Suppl:887S-968S.
- [12]Hirsh J,Raschke R.Heparin and low-molecular-weight heparin:the Seventh ACCP Conference on Antithrombotic and Thrombo-lytic Therapy.Chest,2004,1263Suppl:188S-203S.
- [13]Haas S,Breyer HG,Bacher HP,et al.Prevention of major ve-nous thromboembolism following total hip or knee replacement:a randomized comparison of low-molecular-weight heparin with un-fractionated heparin(ECHOS Trial).Int Angiol,2006,25:335-342.
- [14]Ontalescot G,Polle V,Collet JP,et al.Low molecular weight heparin after mechanical heart valve replacement.Circulation,2000,101:1083-1086.
- [15]Bauman ME,Belletrutti MJ,Bajzar L,et al.Evaluation of enox-aparin dosing requirements in infants and children.Better dosing to achieve therapeutic levels.Thromb Haemost,2009,101:86-92.
- [16]张志宏,覃军,黄岚,等.儿童房间隔缺损封堵术后低分子肝素抗凝疗效分析.第三军医大学学报,2008,9:858-860.
- [17]De Candia E,De Cristofaro R,Landolfi R,et al.Thrombin-in-duced platelet activation is inhibited by high-and low-molecular-weight heparin.Circulation,1999,99:3308-3314.
- [18]Rodés-Cabau J,Palacios A,Palacio C,et al.Assessment of the markers of platelet and coagulation activation following transcath-eter closure of atrial septal defects.Int J Cardiol,2005,98:107-112.
- [19]杨荣,盛燕辉,曹克将,等.房间隔缺损患者介入封堵术后血栓前高凝血状态的研究.中国现代医学杂志,2009,3:398-401.