...
首页> 外文期刊>Journal of neuroimaging >Ultrasound-enhanced thrombolysis for acute ischemic stroke: phase I. Findings of the CLOTBUST trial.
【24h】

Ultrasound-enhanced thrombolysis for acute ischemic stroke: phase I. Findings of the CLOTBUST trial.

机译:超声增强的溶栓治疗急性缺血性中风:I期。CLOTBUST试验的结果。

获取原文
获取原文并翻译 | 示例

摘要

BACKGROUND: Tissue plasminogen activator (TPA) activity may be enhanced with ultrasound, potentially 2 MHz transcranial Doppler (TCD). The authors present Phase I data of the CLOTBUST (Combined Lysis of Thrombus in Brain ischemia using transcranial Ultrasound and Systemic TPA). SUBJECTS AND METHODS: Nonrandomized stroke patients with proximal arterial occlusion on a prebolus TCD receiving intravenous 0.9 mg/kg TPA within 3 hours after stroke onset were monitored with portable diagnostic TCD equipment and a standard headframe. Complete recanalization was defined as thrombolysis in brain ischemia (TIBI) flow grades 4-5. RESULTS: 55 patients (mean age 69 +/- 15 years, median baseline NIH Stroke Scale [NIHSS] 18, range 4-29, 90% with 3 9 points) were treated at 125 +/- 36 minutes from symptom onset. TCD monitoring began at 117 +/- 39 minutes. Complete recanalization on TCD within 2 hours after bolus was found in 20 patients (36%). Dramatic recovery (NIHSS score < or = 3) occurred in 20% at 2 hours and in 24% at 24 hours. Overall improvement by > or = 4 NIHSS points was found in 49% at 24 hours. Improvement was associated with recanalization during or shortly after TPA infusion (phi r2 = .5, P = .03); however, in 6/20 patients with complete recanalization (30%), no immediate clinical change was noticed within 2 hours. Overall symptomatic hemorrhage rate was 5.5%. CONCLUSIONS: Continuous TCD insonation for up to 2 hours at maximum intensities allowed by current bio-safety guidelines is safe. Dramatic recovery and complete recanalization shortly after TPA bolus are feasible goals for thrombolysis given with TCD monitoring.
机译:背景:组织纤溶酶原激活物(TPA)的活性可能会通过超声(可能是2 MHz的经颅多普勒超声(TCD))得到增强。作者介绍了CLOTBUST(使用经颅超声和全身TPA在脑缺血中的血栓合并溶解)的I期数据。研究对象和方法:使用便携式诊断性TCD设备和标准头架,对在卒中发作后3个小时内接受0.9 mg / kg TPA静脉内注射的无剂量卒中前CDC的非随机卒中患者进行监测。完全再通定义为4-5级脑缺血(TIBI)溶栓。结果:55例患者(平均年龄69 +/- 15岁,中位基线NIH卒中量表[NIHSS] 18,范围4-29,90%,3 9分)在症状发作后125 +/- 36分钟接受了治疗。 TCD监测始于117 +/- 39分钟。在推注后2小时内,对TCD进行了完全再通,发现20例患者(36%)。戏剧性恢复(NIHSS得分<或= 3)在2小时时发生率为20%,在24小时时发生率为24%。在24小时内发现49%的患者的总体改善幅度大于或等于4个NIHSS点。 TPA输注过程中或输注后的再通气与改善相关(phi r2 = 0.5,P = .03);然而,在完全再通的6/20患者中(30%),在2小时内没有发现立即的临床改变。总体症状性出血率为5.5%。结论:以当前生物安全指南允许的最大强度连续2小时进行TCD超声治疗是安全的。在TPA推注之后不久,戏剧性的恢复和彻底的再通是通过TCD监测实现溶栓的可行目标。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号