在班加罗尔举行的印度国家中风会议(INSC)摘要

J. Pandian, J. Bernhardt
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引用次数: 0

摘要

摘要编号:1报告作者:Deepti Vibha电子邮件:deeptivibha@gmail.com研究所:全印度医学科学研究所,新德里,印度编号:1报告作者:Deepti Vibha电子邮件:deeptivibha@gmail.com研究所:全印度医学科学研究所,新德里,印度摘要标题:在6至24小时时间窗内接受血管内治疗的资格:标题:6-24小时时间窗内接受血管内治疗的资格:印度综合卒中中心的回顾性分析简介:DAWN(6-24小时)和defus3试验(6-16小时)将血管内取栓的时间窗延长了四倍,达到24小时。目的:确定综合卒中中心6-24小时时间窗内符合取栓条件的患者的患病率。材料和方法:对2017年7月至2019年9月期间入院的急性缺血性卒中(AIS)患者进行回顾性分析。根据DAWN和/或DEFUSE-3试验标准探讨血栓切除术的资格。临床试验特异性选择标准基于是否存在大血管闭塞、基线修正Rankin量表评分和Alberta卒中项目早期计算机断层扫描评分(ASPECTS)。结果:在研究期间入院的260例AIS患者中,32.7% (n = 85)在6 ~ 24小时时间窗内出现,72.3% (n = 188)的美国国立卫生研究院卒中量表(NIHSS)≥6。根据NIHSS和时间窗标准,分别有16.9%(44例)和17.7%(46例)的患者可能符合DAWN和DEFUSE-3试验标准。此外,3.1%(8/260)和2.7%(7/260)的患者符合DAWN和DEFUSE-3试验标准,包括存在前循环大血管闭塞和ASPECTS≥6。在6-24 h窗期(85),分别有9.4%(8/85)和8.2%(7/85)的患者符合DAWN和DEFUSE-3标准。结论:所有在6-24小时内到单一综合卒中中心就诊的AIS患者中,分别有9.4%和8.2%的患者符合DAWN和DEFUSE-3临床试验标准。这些数据预测了印度窗后血栓切除术的巨大潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstracts from the Indian National Stroke Conference (INSC) Held in Bangalore
s from the Indian National Stroke Conference (INSC) Held in Bangalore Abstract Number: 1 Presenting author: Deepti Vibha Email: deeptivibha@gmail.com Institute: All India Institute of Medical Sciences, New Delhi, IndiaNumber: 1 Presenting author: Deepti Vibha Email: deeptivibha@gmail.com Institute: All India Institute of Medical Sciences, New Delhi, India Abstract Title: Eligibility for Endovascular Treatment in the 6to 24-h Time Window: Retrospective Analysis of a Comprehensive Stroke Center in IndiaTitle: Eligibility for Endovascular Treatment in the 6to 24-h Time Window: Retrospective Analysis of a Comprehensive Stroke Center in India Introduction: The DAWN (6-24 h) and the DEFUSE-3 trials (6-16 h) have quadrupled the time window for endovascular thrombectomy up to 24 h. Aim: To identify the prevalence of thrombectomy-eligible patients in the 6-24-h time window at a comprehensive stroke center. Materials and Methods: A retrospective review of acute ischemic stroke (AIS) admissions was performed between July 2017 and September 2019. Eligibility for thrombectomy was explored based on DAWN and/or DEFUSE-3 trial criteria. Clinical trial-specific selection criteria were applied based on the presence of large vessel occlusion, baseline modified Rankin Scale score, and the Alberta Stroke Program Early Computerized Tomography Score (ASPECTS). Results: Out of 260 patients with AIS admitted within the study period, 32.7% (n = 85) presented within the 6to 24-h time window, and 72.3% (n = 188) had a National Institutes of Health Stroke Scale (NIHSS) ≥6. Based on NIHSS and time window criteria, 16.9% (44) and 17.7% (46) patients were potentially eligible for DAWN and DEFUSE-3 trial criteria, respectively. Further, 3.1% (8/260) and 2.7% (7/260) patients met DAWN and DEFUSE-3 trial criteria, including presence of anterior circulation large vessel occlusion and ASPECTS ≥6. In the 6-24-h window (85), 9.4% (8/85) and 8.2% (7/85) of patients met DAWN and DEFUSE-3 criteria, respectively. Conclusions: Of all patients with AIS presenting to a single comprehensive stroke center in the 6-24-h window, 9.4% and 8.2% of patients qualified for DAWN and DEFUSE-3 clinical trial criteria, respectively. These data predict a large potential for late-window thrombectomy in India.
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