Department of Radiology, Sacred Heart Medical Center, 101 West Eighth Avenue, PO Box 2555, Spokane, WA 99220-2555, USA.
J Vasc Interv Radiol. 2010 Aug;21(8):1165-72. doi: 10.1016/j.jvir.2010.03.020.
This study retrospectively assesses whether significantly accelerating thrombolysis with ultrasound affects fibrinogen levels in the treatment of peripheral arterial occlusions.
Between December 2005 and August 2007, 38 limbs in 38 patients (17 women; mean age, 60.5 +/- 19.7 years; age range, 17-94 years) were treated with ultrasound-accelerated thrombolysis for peripheral arterial occlusion (PAO) and deep vein thrombosis (DVT), with serum fibrinogen levels measured at baseline and every 24 hours. All occlusions were treated with alteplase (0.5-1.0 mg/h).
Complete or partial lysis was achieved in 92.1% of patients. All patients received thrombolytic therapy with mean infusion time of 42.3 hours (range, 20-96 hours). As part of standard clinical practice, patients were not assessed angiographically overnight. Mean total alteplase dose was 40.6 mg (range, 18-96 mg). Across all patients, the fibrinogen level at the end of infusion decreased by an average of 18.5% from baseline, and no patient exhibited a fibrinogen level < 100 mg/dL during treatment. Fibrinogen depletion was more pronounced among patients with venous occlusions (26.4% from baseline) than those with arterial occlusions (15.8% from baseline). No major hemorrhagic complications occurred. One patient (2.6%) experienced a minor bleeding event at the access site, and use of thrombolytics was discontinued; and one patient with a chronic arterial occlusion and underlying coronary disease who did not respond to thrombolytic therapy, experienced an acute myocardial infarction. Of documented 30-day clinical outcomes in 20 patients, 80.0% remained patent at 30 days.
Ultrasound-accelerated thrombolysis for the treatment of PAO and DVT is associated with a very low complication rate and nominal fibrinogen depletion.
本研究通过回顾性评估,探讨外周动脉闭塞(PAO)和深静脉血栓形成(DVT)患者应用超声加速溶栓治疗时,纤维蛋白原水平是否会显著改变。
2005 年 12 月至 2007 年 8 月,对 38 例(17 例女性;平均年龄 60.5±19.7 岁;年龄范围 17-94 岁)PAO 和 DVT 患者采用超声加速溶栓治疗,在基线及每 24 小时检测血清纤维蛋白原水平。所有闭塞均采用组织型纤溶酶原激活物(alteplase)治疗(0.5-1.0mg/h)。
92.1%的患者完全或部分再通。所有患者的溶栓治疗平均输注时间为 42.3 小时(20-96 小时)。根据标准临床实践,患者在夜间未接受血管造影评估。平均总组织型纤溶酶原激活物剂量为 40.6mg(18-96mg)。所有患者的纤维蛋白原水平在输注结束时较基线平均下降 18.5%,且治疗过程中无一例患者纤维蛋白原水平<100mg/dL。静脉闭塞患者的纤维蛋白原消耗(较基线下降 26.4%)比动脉闭塞患者(较基线下降 15.8%)更明显。无重大出血并发症发生。1 例(2.6%)患者在入路部位发生轻微出血事件,停止使用溶栓药物;1 例慢性动脉闭塞和潜在冠状动脉疾病患者对溶栓治疗无反应,发生急性心肌梗死。20 例患者中有 30 天临床结果记录,80.0%的患者在 30 天保持通畅。
超声加速溶栓治疗 PAO 和 DVT 的并发症发生率非常低,纤维蛋白原消耗程度较小。