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首页> 外文期刊>Journal of stroke and cerebrovascular diseases: The official journal of National Stroke Association >Intravenous thrombolysis with neuroprotective therapy by edaravone for ischemic stroke patients older than 80 years of age
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Intravenous thrombolysis with neuroprotective therapy by edaravone for ischemic stroke patients older than 80 years of age

机译:依达拉奉静脉溶栓联合神经保护疗法治疗80岁以上缺血性中风患者

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Background: Alteplase, a recombinant tissue plasminogen activator (tPA), was approved for patients with acute ischemic stroke within 3 hours of stroke onset in Japan in October 2005 at a dose of 0.6 mg/kg. The aim of this study was to assess the safety and efficacy of alteplase in elderly patients in Japan. Methods: One hundred twenty-nine consecutive patients who were admitted to our 5 hospital groups and who received intravenous tPA within 3 hours of stroke onset between January 2010 and December 2011 were divided into 2 groups by age (<80 years of age [younger group] and >80 years of age [older group]) and by treatment with or without edaravone. Clinical backgrounds and outcomes were investigated. Results: The National Institutes of Health Stroke Scale score on admission was not different in both groups, but the National Institutes of Health Stroke Scale scores 7 days after stroke onset were significantly higher in the older group (score 8; P <.05) than in the younger group (score 4), and the ratio of patients with a modified Rankin Scale score of 4 to 6 was significantly greater in the older group (41.7%; P <.05) than in the younger group (22.2%). However, there was no difference in asymptomatic and symptomatic intracerebral hemorrhage rates between the younger and older groups (asymptomatic 20.2% v 18.8%; symptomatic 2.6% v 2.1%). Patients with edaravone showed a higher recanalization rate (61.9%; P <.01) and a better modified Rankin Scale score at 3 months poststroke (P <.01) than the nonedaravone group. Conclusions: These data suggest that intravenous alteplase (0.6 mg/kg) within 3 hours of stroke onset was safe and effective, even for very old patients (≥80 years of age), but resulted in poor outcomes relating not to tPA but to aging. In addition, edaravone may be a good partner for combination therapy with tPA to enhance recanalization and reduce hemorrhagic transformation.
机译:背景:2005年10月,重组中的纤溶酶原激活物(tPA)阿替普酶以0.6 mg / kg的剂量在日本于卒中发作的3小时内被批准用于急性缺血性卒中患者。这项研究的目的是评估阿替普酶在日本老年患者中的安全性和有效性。方法:将2010年1月至2011年12月在中风发作后3小时内入院并连续tPA的129例患者按年龄(<80岁[年轻组]分为两组。 ]和> 80岁的年龄[老年组]),并接受或不接受依达拉奉治疗。临床背景和结果进行了调查。结果:美国国立卫生研究院卒中量表评分两组均无差异,但老年组卒中发生后7天的美国国立卫生研究院卒中量表评分显着高于老年组(得分8; P <.05)。在年轻组中(得分4),Rankin量表修正得分为4到6的患者比例在老年组(41.7%; P <.05)显着高于年轻组(22.2%)。然而,年轻组和老年组之间无症状和有症状的脑出血发生率没有差异(无症状的20.2%vs 18.8%;有症状的2.6%v 2.1%)。与非那达拉奉组相比,依达拉奉患者卒中后3个月的再通率(61.9%; P <.01)和改良的Rankin Scale评分更高(P <.01)。结论:这些数据表明,即使在非常老的患者(≥80岁)中,卒中发作后3小时内静脉使用阿替普酶(0.6 mg / kg)也是安全有效的,但导致不良后果与tPA无关,而与衰老有关。此外,依达拉奉可能是与tPA联合治疗以增强再通和减少出血性转化的良好伴侣。

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