首页> 外文期刊>Journal of stroke and cerebrovascular diseases: The official journal of National Stroke Association >Clinical Deterioration and Early Imaging Changes after Intravenous Tissue Plasminogen Activator Administration in Acute Ischemic Stroke Patients
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Clinical Deterioration and Early Imaging Changes after Intravenous Tissue Plasminogen Activator Administration in Acute Ischemic Stroke Patients

机译:急性缺血性中风患者静脉组织纤溶酶原激活物给药后的临床恶化和早期影像学改变

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Background and Purpose: Clinical worsening is a known complication following acute ischemic stroke. This study attempted to determine the mechanism of deterioration by correlating clinical findings with changes on computed tomography or magnetic resonance. Methods: From a single university medical center, 30 consecutive acute ischemic stroke patients who received intravenous tissue plasminogen activator within 3 hours of symptom onset during a 3-year period were identified from a quality database that included all hospitalized patients either admitted with strokes or with in-hospital strokes. Images were reviewed by a single neuroradiologist for changes including edema, extension of infarct, hemorrhage, herniation, and midline shift and were correlated to National Institutes of Health Stroke Scale (NIHSS) scores obtained from data in the medical chart. Results: Ten patients had documented clinical deterioration with a corresponding increase in the NIHSS score. Of these, 4 patients had follow-up scans that showed worsening changes concurrent with deterioration. In the 20 patients who remained clinically stable, 3 patients had worsening changes on follow-up scans. Patients who deteriorated were no more likely to have imaging changes than those who had a stable clinical course. Appearance of herniation, both subfalcine and uncal, was the only specific imaging change associated with clinical deterioration. Conclusions: This study demonstrates that processes besides hemorrhage, including edema, midline shift, herniation, extension of infarct, and new infarct, are neither frequent nor specific for predicting clinical course. Other factors associated with these processes that may or may not be quantifiable on imaging are likely involved. Furthermore, in over half of the cases of worsening, deterioration occurs without associated imaging, metabolic, or infectious etiologies. (C) 2016 National Stroke Association. Published by Elsevier Inc. All rights reserved.
机译:背景与目的:临床恶化是急性缺血性卒中后的已知并发症。这项研究试图通过将临床发现与计算机断层扫描或磁共振检查的变化相关联来确定恶化的机制。方法:从一个单一的大学医学中心,从质量数据库中识别出30名连续3次在症状发作3小时内接受静脉组织纤溶酶原激活剂的急性缺血性卒中患者,该数据库包括所有因卒中或卒中而入院的住院患者住院中风。图像由一位神经放射科医生检查,以检查其变化,包括水肿,梗塞扩展,出血,疝气和中线移位,并与从医学图表中的数据获得的美国国立卫生研究院卒中量表(NIHSS)评分相关。结果:十名患者的临床表现恶化,NIHSS评分相应升高。其中,有4名患者进行了随访扫描,发现变化加重同时恶化。在20例保持临床稳定的患者中,有3例在随访扫描中出现了恶化的变化。与那些病情稳定的患者相比,病情恶化的患者发生影像学改变的可能性较小。亚法辛和非法尔疝的出现是与临床恶化相关的唯一特异性影像学改变。结论:这项研究表明,除了出血以外的其他过程,包括水肿,中线移位,疝气,梗死范围扩大和新发梗死,都不是经常性的,也不是预测临床病程的特异性。可能涉及与这些过程相关的其他因素,这些因素在成像时可能无法量化。此外,在一半以上的恶化病例中,恶化没有相关的影像学,代谢或传染病因。 (C)2016年全国中风协会。由Elsevier Inc.出版。保留所有权利。

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