Cruz-Gonzalez Ignacio, Sanchez-Ledesma Maria, Osakabe Masanori, Watanabe Hikari, Baron Suzanne J, Healy Josephine L, Yeh Robert W, Jang Ik-Kyung
Cardiology Division, Massachusetts General Hospital, Harvard Medical School. Boston, Massachusetts, USA.
Blood Coagul Fibrinolysis. 2008 Jul;19(5):401-4. doi: 10.1097/MBC.0b013e328304e00d.
Argatroban is increasingly used in patients with heparin-induced thrombocytopenia. Although the recommended activated clotting time during percutaneous coronary intervention is 300-450 s, this recommendation is based on the limited data. This single-center, retrospective study evaluated the efficacy (composite of death, myocardial infarction, or urgent revascularization) and safety (evaluated by thrombolysis in myocardial infarction major bleeding) of argatroban during percutaneous coronary intervention according to activated clotting time levels. Patients were divided into three groups according to the activated clotting time achieved during the procedure (<300s, 300-450s, and >450 s). In this study, 120 consecutive patients with confirmed or suspected heparin-induced thrombocytopenia received argatroban (241 +/- 104 mug/kg bolus, followed by a 18 +/- 10 microg/kg per min infusion) during percutaneous coronary intervention. The indication for percutaneous coronary intervention was stable angina in 20% of patients, unstable angina or non-ST elevation myocardial infarction in 58%, and ST elevation myocardial infarction in 22%. An adjunctive glycoprotein IIb/IIIa inhibitor was used in 56 patients (46.7%). When divided into three groups on the basis of the activated clotting time (<300, 300-450, >450 s), no significant difference was observed between the groups in the efficacy endpoint, which occurred in 9.8% (6/61) of patients in the group with activated clotting time less than 300 s, 19.6% (9/46) of patients in the group with activated clotting time 300-450 s, and 7.7% (1/13) of patients in the group with activated clotting time more than 450 s (P = 0.58). The rate of major bleeding was higher in the group of patients with activated clotting time more than 450 s (1.6, 0, and 15.4% patients, respectively; P = 0.006). These results suggest that in patients undergoing percutaneous coronary intervention, argatroban provides adequate anticoagulation with a low bleeding rate, when activated clotting time is maintained below 450 s.
阿加曲班越来越多地用于肝素诱导的血小板减少症患者。尽管经皮冠状动脉介入治疗期间推荐的活化凝血时间为300 - 450秒,但该推荐基于有限的数据。这项单中心回顾性研究根据活化凝血时间水平评估了阿加曲班在经皮冠状动脉介入治疗期间的疗效(死亡、心肌梗死或紧急血运重建的复合终点)和安全性(通过心肌梗死溶栓严重出血进行评估)。根据手术期间达到的活化凝血时间将患者分为三组(<300秒、300 - 450秒和>450秒)。在本研究中,120例连续的确诊或疑似肝素诱导的血小板减少症患者在经皮冠状动脉介入治疗期间接受了阿加曲班(241±104微克/千克推注,随后以18±10微克/千克每分钟的速度输注)。经皮冠状动脉介入治疗的适应证为20%的患者为稳定型心绞痛,58%为不稳定型心绞痛或非ST段抬高型心肌梗死,22%为ST段抬高型心肌梗死。56例患者(46.7%)使用了糖蛋白IIb/IIIa抑制剂。根据活化凝血时间(<300、300 - 450、>450秒)分为三组时,各治疗组在疗效终点方面未观察到显著差异,活化凝血时间小于300秒的组中9.8%(6/61)的患者出现该终点,活化凝血时间为300 - 450秒的组中19.6%(9/46)的患者出现该终点,活化凝血时间大于450秒的组中7.7%(1/13)的患者出现该终点(P = 0.58)。活化凝血时间大于450秒的患者组严重出血发生率更高(分别为1.6%、0和15.4%;P = 0.006)。这些结果表明,在接受经皮冠状动脉介入治疗的患者中,当活化凝血时间维持在450秒以下时,阿加曲班可提供充分的抗凝作用且出血率较低。