摘要编号:LBA19接受替萘普酶治疗的急性缺血性脑卒中患者颅内出血的全网发病率

IF 2.1 Q3 CLINICAL NEUROLOGY
Farah Fourcand, S. Sahito, ChHassan Ali, E. Marandi, Joshua Haimi, I. Dubinsky, Yong-Bum Song, S. Mehta, N. Tabibzadeh, Nancy E Gadallah, Spozhmy Panezai, J. Kirmani
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引用次数: 0

摘要

静脉注射替萘普酶(TNK)目前被用作急性缺血性中风(AIS)的溶栓剂,根据最近的研究,它已被证明不劣于静脉注射阿替普酶。作为阿替普酶并发症的颅内出血(ICH)约占6%。我们研究的目的是确定在现实世界中接受TNK治疗的AIS患者的显著ICH发生率。使用Get With the Guidelines数据库对2020年2月至2022年1月接受TNK治疗的患者进行了全网络(3个CSC,6个PSC)、多中心回顾性图表审查。根据全网络政策,TNK剂量为0.25mg/kg。ICH采用ECASS‐3标准进行分类。Fisher精确检验统计量用于确定ICH的存在与基线ASPECTS评分、血管内治疗(EVT)和静脉注射依非巴特之间是否存在显著关联。根据我们网络中与阿替普酶相关的PH-2发病率,设定了低于2%的PH-2发生率基准。社会科学统计软件用于数据分析。在180名接受TNK治疗的患者中,25名受试者(13.89%)出现出血性转化。平均年龄为71.88岁(95%CI 65.54,78.22)。48%的受试者为女性。ASPECTS评分中位数为8(95%CI 7.54,8.78)。90天平均mRS中位数为3(95%CI 2.1,3.9)。出血性转化分为HI-1(5%,n=9)、HI-2(1.7%,n=3)、PH-1(3.8%,n=7)和PH-2(3.3%,n=6)。当调整ASPECTS评分>=7与<7(Fisher值=1)、EVT与无EVT(Fisher值=0.65)、,或静脉注射依非巴特(Fisher值=0.06)。与阿替普酶相关的PH-2的基准发生率相比,替萘普酶与较高的PH-2颅内出血率相关。本研究受到样本量小、回顾性和非受控变量的显著限制。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: LBA19 Network‐Wide Incidence of Intracranial Hemorrhage in Patients with Acute Ischemic Stroke Receiving Tenecteplase
Intravenous tenecteplase (TNK) is currently being used as a thrombolytic agent in acute ischemic stroke (AIS) and has has been shown to be non‐inferior to intravenous alteplase according to recent studies. Intracranial hemorrhage (ICH) as a complication of alteplase is approximately at 6%. The aim of our study was to determine the rate of significant ICH in patients receiving TNK indicated for AIS in a real world setting. A network‐wide (3 CSCs, 6 PSCs), multicenter retrospective chart review of patients receiving TNK from February 2020 to January 2022 was performed using the Get With The Guidelines database. TNK bolus dose of 0.25mg/kg was used according to a network‐wide policy. ICH was categorized using ECASS‐3 criteria. Fisher exact test statistic was used to determine if a significant association existed between the presence of ICH and baseline ASPECTS score, endovascular treatment (EVT), and IV eptifibatide use. A benchmark less than 2% PH‐2 incidence was set based on historical alteplase related PH‐2 rates within our network. Social science statistics software was used for data analysis. Out of 180 patients who received TNK, 25 subjects (13.89%) developed hemorrhagic transformation. Mean age was 71.88 (95% CI 65.54, 78.22). Forty‐eight percent of subjects were female. Median ASPECTS score was 8 (95% CI 7.54, 8.78). Median 90 day mRS was 3 (95% CI 2.1, 3.9). Hemorrhagic transformation was classified as HI‐1 in 5% (n = 9), HI‐2 in 1.7% (n = 3), PH‐1 in 3.8% (n = 7), and PH‐2 in 3.3% (n = 6) subjects. No significant difference between subjects with other subtypes versus PH‐2 was identified when adjusting for ASPECTS score > = 7 versus < 7 (Fisher value = 1), EVT versus no EVT (Fisher value = 0.65), or use of IV eptifibatide (Fisher value = 0.06). Tenecteplase is associated with higher rates of PH‐2 intracranial hemorrhage when compared with our benchmark rates of alteplase‐related PH‐2. This study is significantly limited by small sample size, retrospective nature, and uncontrolled variables. Larger, prospective studies are needed to validate our results.
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