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超声识别与溶解血栓。

Ultrasound identification and lysis of clots.

作者信息

Alexandrov Andrei V

机构信息

Department of Neurology and Radiology, Cerebrovascular Ultrasound and Center for Noninvasive Brain Perfusion Studies, Stroke Treatment Team, The University of Texas-Houston Medical School, Houston, Texas, USA.

出版信息

Stroke. 2004 Nov;35(11 Suppl 1):2722-5. doi: 10.1161/01.STR.0000143321.37482.b3. Epub 2004 Sep 16.

Abstract

Poor recovery after systemic tissue plasminogen activator (tPA) therapy could result from the initial severity of ischemic insult and slow and incomplete thrombolysis. Persisting arterial occlusions can be identified at bedside using portable diagnostic ultrasound by detecting residual flow signals around the thrombus (thrombolysis in brain ischemia [TIBI] flow grades). A narrow pulsed ultrasound beam can be steadily aimed at the thrombus/residual flow interface, exposing more thrombus surface and structures to tPA, and tPA activity can be enhanced with 2 MHz transcranial Doppler (TCD). A randomized, multicenter, clinical trial called CLOTBUST (Combined Lysis of Thrombus in Brain ischemia using transcranial Ultrasound and Systemic tPA) trial showed a 49% rate of complete recanalization or dramatic clinical recovery from stroke within 2 hours after tPA bolus when tPA infusion was continuously monitored with TCD, compared with 30% among patients who received tPA without ultrasound monitoring (P=0.03, number needed to treat, 5). Early complete recanalization was sustained at 2 hours by 38% of monitored patients compared with 12.7% controls. The CLOTBUST Trial showed a trend toward sustaining complete recovery at 3 months (41.5% versus 28%, modified Rankin Scale scores 0 to 1), subject for a pivotal phase III trial. Ultrasound is an inexpensive, noninvasive, real-time monitoring tool to identify nonresponders to systemic tPA and select patients with persisting occlusions for intraarterial interventions. Early brain perfusion augmentation, complete recanalization, and dramatic clinical recovery are feasible goals for ultrasound-enhanced thrombolysis.

摘要

全身组织型纤溶酶原激活剂(tPA)治疗后恢复不佳可能是由于缺血性损伤的初始严重程度以及溶栓缓慢和不完全所致。通过便携式诊断超声检测血栓周围的残余血流信号(脑缺血溶栓 [TIBI] 血流分级),可在床边识别持续性动脉闭塞。窄脉冲超声束可稳定地对准血栓/残余血流界面,使更多血栓表面和结构暴露于tPA,并且使用2兆赫经颅多普勒(TCD)可增强tPA活性。一项名为CLOTBUST(使用经颅超声和全身tPA联合溶解脑缺血血栓)的随机、多中心临床试验表明,当用TCD持续监测tPA输注时,在tPA推注后2小时内,完全再通率或卒中后显著临床恢复率为49%,而未进行超声监测的tPA治疗患者为30%(P = 0.03,需治疗人数为5)。38%的监测患者在2小时时维持早期完全再通,而对照组为12.7%。CLOTBUST试验显示在3个月时维持完全恢复有一定趋势(改良Rankin量表评分0至1,分别为41.5%对28%),有待进行关键的III期试验。超声是一种廉价、无创的实时监测工具,可识别对全身tPA无反应者,并选择有持续性闭塞的患者进行动脉内干预。早期脑灌注增加、完全再通和显著临床恢复是超声增强溶栓的可行目标。

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