Terry Kimberly J, Buckley Leo F, Aldemerdash Ahmed, Fanikos John, Dell'Orfano Heather
Department of Pharmacy, University of Utah, Salt Lake City, UT, United States.
Department of Pharmacotherapy and Outcomes Science, Virginia Commonwealth University, Richmond, VA, United States.
Cardiovasc Hematol Disord Drug Targets. 2017;17(2):132-135. doi: 10.2174/1871529X17666170908110328.
Ultrasound-assisted, catheter-directed thrombolysis (UA-CDT) relieves right ventricular stress without a significant increase in the risk of bleeding compared to systemic thrombolysis. Although concomitant anticoagulation is provided to prevent thrombus expansion, the optimal anticoagulation regimen in patients receiving UA-CDT remains unknown.
We sought to describe anticoagulation practices for patients receiving UA-CDT.
Patients receiving UA-CDT for acute pulmonary embolism (PE) between Jan 1, 2013 to Sept 30, 2014 at a single center were analyzed. We collected patient characteristics, fibrinolytic and anticoagulant usage as well as clinical outcomes.
Fourteen patients were included in the final analysis. The mean alteplase dose was 16.8 ± 5.6 mg and 24.3 ± 3.4 mg in unilateral and bilateral PE, respectively. Mean unfractionated heparin (UFH) rates were 7.4 (±2.17) IU/kg/hr and 12.4 (±3.1) IU/kg/hr during and after fibrinolytic therapy, respectively. The median aPTT was 42.4 sec [IQR 34.5-51.8] and 77.9 sec [IQR 66.5-96.8] during and after fibrinolytic therapy, respectively. There were no recurrent VTE within 30 days of hospital discharge. One patient had a major bleeding event (intracranial hemorrhage).
In patients with acute PE, our institution utilized low levels of anticoagulation during fibrinolytic administration and therapeutic doses after completion of fibrinolytic infusion. Standardized protocols for anticoagulation during UA-CDT are warranted.
与全身溶栓相比,超声辅助导管定向溶栓(UA-CDT)可减轻右心室压力,且出血风险无显著增加。尽管会进行联合抗凝以防止血栓扩展,但接受UA-CDT治疗的患者的最佳抗凝方案仍不明确。
我们试图描述接受UA-CDT治疗的患者的抗凝实践。
分析了2013年1月1日至2014年9月30日在单一中心接受UA-CDT治疗急性肺栓塞(PE)的患者。我们收集了患者特征、纤溶和抗凝药物使用情况以及临床结局。
14例患者纳入最终分析。单侧和双侧PE患者的阿替普酶平均剂量分别为16.8±5.6mg和24.3±3.4mg。纤溶治疗期间和之后,普通肝素(UFH)的平均输注速率分别为7.4(±2.17)IU/kg/小时和12.4(±3.1)IU/kg/小时。纤溶治疗期间和之后,活化部分凝血活酶时间(aPTT)的中位数分别为42.4秒[四分位间距34.5 - 51.8]和77.9秒[四分位间距66.5 - 96.8]。出院后30天内无复发性静脉血栓栓塞事件。1例患者发生严重出血事件(颅内出血)。
在急性PE患者中,我们机构在纤溶给药期间使用低剂量抗凝,纤溶输注完成后使用治疗剂量。UA-CDT期间的标准化抗凝方案是必要的。