血管内取栓与药物治疗对中度血管闭塞继发缺血性脑卒中的预后

IF 2.1 Q3 CLINICAL NEUROLOGY
Farah Fourcand, Sean Scarpiello, Abdallah O Amireh, Thomas Snyder, Shrinjay Vyas, Rudra Joshi, I. Dubinsky, Brigitte Percival, H. Zacharatos, S. Mehta, J. Kirmani
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引用次数: 0

摘要

急性缺血性脑卒中(AIS)由动脉闭塞治疗急诊血管内血栓切除术(EVT)当临床适当。与大血管闭塞(LVO)相比,EVT在中血管闭塞(MVO)中的临床结果既没有得到很好的确定,也没有与其他医疗管理进行比较。我们的目的是评估继发于MVO的AIS患者接受EVT的结果。我们对到我们的综合卒中中心就诊的MVO相关AIS患者进行了回顾性图表回顾,这些患者接受了EVT或积极的动脉内溶栓治疗,同时给予静脉注射依替巴肽。我们评估了闭塞部位、NIHSS(出现,7天或出院,3个月)、改良Rankin量表(基线,90天)和颅内出血(ICH)率。MVO定义为单纯的M2大脑中动脉闭塞,不累及M1段、大脑前动脉A1段或更远段、大脑后动脉P1段或更远段。采用Mann - Whitney U检验、Fisher精确检验统计量和T检验统计量进行分析。采用社会科学统计软件进行数据分析。2020年8月至2021年12月,175例EVT患者中,50例发生MVO (n = 33 M2闭塞,n = 12 M3闭塞,P1、P2、A1、A2、A3各n = 1)。12例MVO患者接受积极的医疗管理,同时静脉注射依替巴肽。两组受试者基线时相似(NIHSS中位数为11 [95% CI 10.75, 14.32];平均年龄71.5岁[95% CI 69.24, 73.77];男性48.39% [n = 30])。EVT组初始NIHSS和出院NIHSS的差异有统计学意义(Z‐Score = 4.03;p值< 0.00001),但在医疗组没有(Z - score = 1.96;p值0.05)。EVT组发生出血转化的比例为28% (n = 14),医疗组为16.67% (n = 2)。这没有统计学意义(Fisher值:0.71)。90天mRS中位数为1 (95% CI[0.89, 2.11])。90天mRS之间的差异无显著性差异(Z‐score =‐1.20;p值0.23)。在我们的患者队列中,血管内治疗在中度血管闭塞中是安全的,并且可能具有更有利的临床结果,这一点从血管内血栓切除术组较高的δ NIHSS可以看出。需要更大规模的前瞻性研究来验证我们的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstract Number: LBA7 Outcomes of Endovascular Thrombectomy Versus Medical Treatment in Ischemic Strokes Secondary to Medium Vessel Occlusion
Acute ischemic stroke (AIS) from arterial occlusions are treated with emergent endovascular thrombectomy (EVT) when clinically appropriate. Clinical outcomes of EVT in medium vessel occlusion (MVO) compared to large vessel occlusion (LVO) have neither been well established nor compared to alternate medical management. Our aim was to evaluate outcomes of patients with AIS secondary to MVO undergoing EVT. We conducted a retrospective chart review of patients presenting to our comprehensive stroke center with MVO‐associated AIS undergoing EVT or aggressive intra‐arterial thrombolytic treatment with concurrent administration of IV eptifibatide. We assessed occlusion site, NIHSS (presentation, 7 day or discharge, 3 months), modified Rankin Scale (baseline, 90‐day), and intracranial hemorrhage (ICH) rate. MVO was defined as occlusion of pure M2 middle cerebral artery without M1 segment involvement, anterior cerebral artery A1 segment or more distal, and posterior cerebral artery P1 segment or more distal. Mann‐Whitney U test, Fisher exact test statistic, and T‐test statistic were used for analysis. Social science statistics software was used for data analysis. From August 2020 to December 2021, out of 175 patients who underwent EVT, 50 had MVO (n = 33 M2 occlusion, n = 12 M3 occlusion, n = 1 for P1, P2, A1, A2, A3 each). Twelve subjects with MVO received aggressive medical management with concurrent IV eptifibatide. Subjects between arms were similar at baseline (median NIHSS 11 [95% CI 10.75, 14.32]; mean age 71.5 [95% CI 69.24, 73.77]; male 48.39% [n = 30]). The difference between initial NIHSS and discharge NIHSS was statistically significant in the EVT arm (Z‐Score = 4.03; p‐value < .00001) but not in the medical arm (Z‐score = 1.96; p‐value 0.05). Hemorrhagic transformation occurred in 28% (n = 14) of EVT arm and 16.67% (n = 2) of medical arm. This was not statistically significant (Fisher value: 0.71). Median 90 day mRS was 1 (95% CI [0.89, 2.11]). The difference between 90 day mRS was not significantly different (Z‐score = ‐1.20; p‐value 0.23). In our patient cohort, endovascular therapy was safe in medium vessel occlusion and may have more favorable clinical outcomes as illustrated by higher delta NIHSS in the endovascular thrombectomy group. Larger, prospective studies are needed to validate our results.
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