Evaluation of Door-to-Needle Times Between Alteplase and Tenecteplase for Acute Ischemic Stroke at Two Academic Medical Centers.

IF 2.3 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Nicholas J Monkemeyer, Kaylee K Marino, Melanie Z Goodberlet, Christopher Anderson, Linda Bresette, Andrew J Webb, Aneesh Singhal, Lydia R Ware
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引用次数: 0

Abstract

Background: Off-label tenecteplase use for acute ischemic stroke (AIS) has increased due to ease of administration and comparable efficacy and safety to alteplase.

Objective: This study aimed to evaluate time to thrombolysis before and after transition from alteplase to tenecteplase for treatment of AIS at 2 institutions.

Methods: This retrospective cohort study included adult patients receiving thrombolysis for AIS before and after transition from alteplase to tenecteplase at 2 academic medical centers from January 1, 2020 to January 31, 2024. The primary endpoint was door-to-needle (DTN) time, defined as minutes from hospital arrival to thrombolysis administration. Notable secondary endpoints included time from last known well (LKW) to thrombolysis, time from brain imaging to thrombolysis, hospital length of stay (LOS), and incidence of symptomatic intracranial hemorrhage (sICH).

Results: A total of 328 patients (168 tenecteplase and 160 alteplase) were included. Patients were 51.5% female with a median (interquartile range [IQR]) age of 70 [58-80] years and initial National Institutes of Health Stroke Scale (NIHSS) score of 8 [5-14]. There was no statistically significant difference in DTN time (60 vs 56 minutes), time from LKW to thrombolysis (134 vs 147.5 minutes), or time from brain imaging to thrombolysis (32 vs 31 minutes) between tenecteplase and alteplase. Hospital LOS (5.7 vs 4.9 days) and the rates of sICH (3% vs 3.8%) were similar between groups.

Conclusion and relevance: Tenecteplase and alteplase had comparable DTN times for treatment of AIS and similar safety endpoints. Further studies are warranted to identify opportunities to streamline DTN times with tenecteplase.

在两家学术医疗中心对阿替普酶和替奈替普酶治疗急性缺血性脑卒中的进针时间进行评估。
背景:急性缺血性脑卒中(AIS)标签外使用替奈普酶的情况有所增加,原因是给药方便,且疗效和安全性与阿替普酶相当:本研究旨在评估两家医疗机构从阿替普酶过渡到替奈普酶治疗AIS前后的溶栓时间:这项回顾性队列研究纳入了2020年1月1日至2024年1月31日期间在两家学术医疗中心接受溶栓治疗的成人患者,这些患者在从阿替普酶过渡到替奈替普酶之前和之后接受了溶栓治疗。主要终点是 "门到针"(DTN)时间,即从到达医院到实施溶栓治疗的时间。值得注意的次要终点包括从最后一次已知痊愈(LKW)到溶栓的时间、从脑成像到溶栓的时间、住院时间(LOS)和症状性颅内出血(sICH)的发生率:结果:共纳入328例患者(168例十肽酶、160例阿替普酶)。女性患者占51.5%,中位(四分位间距[IQR])年龄为70[58-80]岁,美国国立卫生研究院卒中量表(NIHSS)初始评分为8[5-14]分。替奈替普酶和阿替普酶的 DTN 时间(60 分钟 vs 56 分钟)、从 LKW 到溶栓的时间(134 分钟 vs 147.5 分钟)以及从脑成像到溶栓的时间(32 分钟 vs 31 分钟)均无统计学差异。两组患者的住院时间(5.7 对 4.9 天)和 sICH 发生率(3% 对 3.8%)相似:特奈普酶和阿替普酶治疗AIS的DTN时间相当,安全性终点相似。有必要开展进一步研究,以确定使用替奈普酶缩短DTN时间的机会。
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来源期刊
CiteScore
5.70
自引率
0.00%
发文量
166
审稿时长
3-8 weeks
期刊介绍: Annals of Pharmacotherapy (AOP) is a peer-reviewed journal that advances pharmacotherapy throughout the world by publishing high-quality research and review articles to achieve the most desired health outcomes.The articles provide cutting-edge information about the most efficient, safe and cost-effective pharmacotherapy for the treatment and prevention of various illnesses. This journal is a member of the Committee on Publication Ethics (COPE). Average time from submission to first decision: 14 days
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