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急性缺血性卒中中联合静脉和动脉溶栓与使用重组组织型纤溶酶原激活剂进行原发性动脉治疗的比较。

Comparison of combined venous and arterial thrombolysis with primary arterial therapy using recombinant tissue plasminogen activator in acute ischemic stroke.

作者信息

Wolfe Thomas, Suarez Jose I, Tarr Robert W, Welter Elisabeth, Landis Dennis, Sunshine Jeffrey L, Zaidat Osama O

机构信息

Department of Neurology, Medical College of Wisconsin/Froedtert Hospital, Milwaukee, Wisconsin 53226, USA.

出版信息

J Stroke Cerebrovasc Dis. 2008 May-Jun;17(3):121-8. doi: 10.1016/j.jstrokecerebrovasdis.2007.12.004.

Abstract

OBJECTIVE

We sought to compare the safety and efficacy of combined intravenous (IV) and intra-arterial (IA) thrombolysis with primary IA therapy using tissue plasminogen activator for acute ischemic stroke presenting within 6 hours of symptom onset.

METHODS

We performed quasirandomization of a single institution's prospectively collected stroke database, comparing IV/IA (0.6 mg/kg IV < or = 60 mg, followed by 0.3 mg/kg IA < or = 30 mg) versus primary IA. Outcome measures include 90-day modified Rankin scale score, mortality, symptomatic intracerebral hemorrhage, and recanalization rates. Statistical analysis was performed using bivariate and propensity score methods.

RESULTS

Of 1057 patients, 41 patients were treated with IV/IA, and 55 with IA. There was significant difference in time to treatment (mean of 151 minutes for the combined group and 261 minutes for the IA, P < .0001) and arterial tissue plasminogen activator dose (17.5 mg for IV/IA v 22.8 mg for IA only, P = .05). Propensity score matching yielded 25 patients in each group. Symptomatic intracerebral hemorrhage rate was 12% in each group. Mortality was 20% in the IV/IA group versus 16% in the IA group (relative risk 1.3 [0.4-4.1], P = .7). More patients in IV/IA group had modified Rankin scale score less than or equal to 2 (odds ratio 1.6 [0.5-5.8], P = .3). Recanalization was 64% with IV/IA versus 48% with IA (odds ratio 1.9 [0.5-7.0], P = .3).

CONCLUSION

This study demonstrates that both combined IV/IA and primary IA recombinant tissue plasminogen activator therapy is feasible and safe in the treatment of acute ischemic stroke. Combined IV/IA therapy may be associated with an improvement in clinical outcome without a significant increase in the risk of symptomatic intracerebral hemorrhage and mortality compared with IA therapy.

摘要

目的

我们旨在比较静脉内(IV)联合动脉内(IA)溶栓与使用组织纤溶酶原激活剂进行原发性IA治疗对症状出现6小时内的急性缺血性卒中的安全性和有效性。

方法

我们对单一机构前瞻性收集的卒中数据库进行了半随机化,比较IV/IA(0.6mg/kg静脉注射≤60mg,随后0.3mg/kg动脉内注射≤30mg)与原发性IA治疗。结局指标包括90天改良Rankin量表评分、死亡率、症状性脑出血和再通率。使用双变量和倾向评分方法进行统计分析。

结果

在1057例患者中,41例接受IV/IA治疗,55例接受IA治疗。治疗时间(联合组平均151分钟,IA组平均261分钟,P<.0001)和动脉组织纤溶酶原激活剂剂量(IV/IA组为17.5mg,仅IA组为22.8mg,P=.05)存在显著差异。倾向评分匹配后每组有25例患者。每组症状性脑出血率均为12%。IV/IA组死亡率为20%,IA组为16%(相对风险1.3[0.4-4.1],P=.7)。IV/IA组更多患者改良Rankin量表评分小于或等于2(优势比1.6[0.5-5.8],P=.3)。IV/IA组再通率为64%,IA组为48%(优势比1.9[0.5-7.0],P=.3)。

结论

本研究表明,IV/IA联合治疗和原发性IA重组组织纤溶酶原激活剂治疗在急性缺血性卒中治疗中都是可行且安全的。与IA治疗相比,IV/IA联合治疗可能与临床结局改善相关,且症状性脑出血和死亡率风险无显著增加。

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