Johns Hopkins Hospital, Baltimore, Maryland, USA.
J Am Coll Cardiol. 2010 May 25;55(21):2376-82. doi: 10.1016/j.jacc.2009.12.056.
This study was designed to assess the risk of significant bleeding complications in patients receiving antiplatelet or anticoagulation medications at the time of implantable cardioverter-defibrillator (ICD) device implantation.
Periprocedural management of antiplatelet or anticoagulation therapy at the time of device implantation remains controversial.
We performed a retrospective chart review of bleeding complications in all patients undergoing ICD or pacemaker implantation from August 2004 to August 2007. Aspirin or clopidogrel use was defined as taken within 5 days of the procedure. A significant bleeding complication was defined as need for pocket exploration or blood transfusion; hematoma requiring pressure dressing or change in anticoagulation therapy; or prolonged hospitalization.
Of the 1,388 device implantations, 71 had bleeding complications (5.1%). Compared with controls not taking antiplatelet agents (n = 255), the combination of aspirin and clopidogrel (n = 139) significantly increased bleeding risk (7.2% vs. 1.6%; p = 0.004). In patients taking aspirin alone (n = 536), bleeding risk was marginally higher than it was for patients taking no antiplatelet agents (3.9% vs. 1.6%, p = 0.078). The use of periprocedural heparin (n = 154) markedly increased risk of bleeding when compared with holding warfarin until the international normalized ratio (INR) was normal (n = 258; 14.3% vs. 4.3%; p < 0.001) and compared with patients receiving no anticoagulation therapy (14.3% vs.1.6%; p < 0.0001). There was no statistical difference in bleeding risk between patients continued on warfarin with an INR > or =1.5 (n = 46) and patients who had warfarin withheld until the INR was normal (n = 258; 6.5% vs. 4.3%; p = 0.50).
Dual antiplatelet therapy and periprocedural heparin significantly increase the risk of bleeding complications at the time of pacemaker or ICD implantation.
本研究旨在评估在植入式心脏复律除颤器(ICD)装置植入时接受抗血小板或抗凝药物治疗的患者发生严重出血并发症的风险。
在装置植入时,抗血小板或抗凝治疗的围手术期管理仍然存在争议。
我们对 2004 年 8 月至 2007 年 8 月期间所有接受 ICD 或起搏器植入的患者进行了出血并发症的回顾性图表审查。阿司匹林或氯吡格雷的使用定义为在手术前 5 天内服用。严重出血并发症定义为需要进行口袋探查或输血;需要加压包扎或改变抗凝治疗的血肿;或延长住院时间。
在 1388 例装置植入中,有 71 例发生出血并发症(5.1%)。与未服用抗血小板药物的对照组(n=255)相比,阿司匹林和氯吡格雷联合使用(n=139)显著增加了出血风险(7.2% vs. 1.6%;p=0.004)。单独服用阿司匹林的患者(n=536)出血风险略高于未服用抗血小板药物的患者(3.9% vs. 1.6%,p=0.078)。与华法林停药直至国际标准化比值(INR)正常(n=258)和未接受抗凝治疗的患者(14.3% vs. 1.6%;p<0.0001)相比,使用围手术期肝素(n=154)明显增加了出血风险。在 INR>或=1.5 的患者(n=46)继续服用华法林和华法林停药直至 INR 正常的患者(n=258)之间,出血风险无统计学差异(6.5% vs. 4.3%;p=0.50)。
双联抗血小板治疗和围手术期肝素显著增加了起搏器或 ICD 植入时出血并发症的风险。