Rousseau Justin F, Weber Jeremy M, Alhanti Brooke, Saver Jeffrey L, Messé Steven R, Schwamm Lee H, Fonarow Gregg C, Sheth Kevin N, Smith Eric E, Mullen Michael T, Silva Gisele Sampaio, Mac Grory Brian, Xian Ying, Warach Steven J
Biostatistics and Clinical Informatics Section, Department of Neurology, University of Texas Southwestern Medical Center, Dallas.
Peter O'Donnell Jr Brain Institute, University of Texas Southwestern Medical Center, Dallas.
JAMA Netw Open. 2025 Mar 3;8(3):e250548. doi: 10.1001/jamanetworkopen.2025.0548.
Tenecteplase is an alternative to alteplase for emergency treatment of acute ischemic stroke. However, limited data are available comparing their clinical effectiveness in routine clinical practice.
To compare short-term effectiveness and safety outcomes for patients with ischemic stroke treated with intravenous tenecteplase vs alteplase.
DESIGN, SETTING, AND PARTICIPANTS: This comparative effectiveness study used data prospectively collected from July 1, 2020, through June 30, 2022, from the Get With The Guidelines-Stroke registry.
Consecutive patients with ischemic stroke treated with either tenecteplase or alteplase within 4.5 hours from last known well time were included.
The primary end point was functional independence on discharge (modified Rankin Scale [mRS] score, 0-2). Secondary effectiveness end points included disability free at discharge (mRS score, 0-1), discharge home, and independent ambulation at discharge. Safety end points included symptomatic intracranial hemorrhage (sICH) within 36 hours and combined in-hospital mortality or hospice discharge. Generalized linear mixed models were fit to evaluate associations between exposure to tenecteplase (vs alteplase) and end points after adjustment for demographic, clinical, and hospital-level variables. Adjusted odds ratios (AORs) with 95% CIs were computed.
Among 79 550 patients treated with intravenous thrombolysis, the mean (SD) age was 68.6 (14.8) years, 38 596 (48.5%) were female, and the median National Institutes of Health Stroke Scale (NIHSS) score was 7 (IQR, 4-13). Of these patients, 9465 (11.9%) received tenecteplase (mean [SD] age, 69.6 [14.7] years; median NIHSS score, 7 [IQR, 4-14]; 4504 [47.6%] female) and 70 085 (88.1%) received alteplase (mean [SD] age, 68.5 [14.8] years; median NIHSS score, 7 [IQR, 4-13]; 34 092 [48.6%] female). After adjustment for covariates, no significant differences were found between tenecteplase and alteplase in effectiveness or safety outcomes for the overall cohort, including functional independence at discharge (AOR, 1.00; 95% CI, 0.93-1.07), sICH (AOR, 0.96; 95% CI, 0.83-1.11), and in-hospital mortality or hospice discharge (AOR, 0.98; 95% CI, 0.89-1.07), but significant improvement was found in discharge home (AOR, 1.26; 95% CI, 1.03-1.53), in-hospital mortality (AOR, 0.63; 95% CI, 0.47-0.85), and composite in-hospital mortality or hospice discharge (AOR, 0.78; 95% CI, 0.62-0.97) among those who were eligible for but did not undergo endovascular thrombectomy.
This large, nationwide comparative effectiveness study using data from routine clinical practice demonstrated similar effectiveness and safety outcomes with tenecteplase compared with alteplase in patients with acute ischemic stroke. This study supports tenecteplase as a reasonable alternative to alteplase.
替奈普酶是急性缺血性卒中紧急治疗中阿替普酶的替代药物。然而,在常规临床实践中比较二者临床疗效的数据有限。
比较静脉注射替奈普酶与阿替普酶治疗缺血性卒中患者的短期疗效和安全性结局。
设计、设置和参与者:这项比较疗效研究使用了从2020年7月1日至2022年6月30日前瞻性收集自“遵循卒中指南”注册研究的数据。
纳入从最后一次已知健康时间起4.5小时内接受替奈普酶或阿替普酶治疗的连续性缺血性卒中患者。
主要终点为出院时功能独立(改良Rankin量表[mRS]评分,0 - 2)。次要疗效终点包括出院时无残疾(mRS评分,0 - 1)、出院回家以及出院时独立行走。安全性终点包括36小时内症状性颅内出血(sICH)以及院内死亡或临终关怀出院的合并情况。采用广义线性混合模型评估在调整人口统计学、临床和医院水平变量后,替奈普酶(与阿替普酶相比)暴露与终点之间的关联。计算调整后的比值比(AOR)及95%置信区间(CI)。
在79550例接受静脉溶栓治疗的患者中,平均(标准差)年龄为68.6(14.8)岁,38596例(48.5%)为女性,美国国立卫生研究院卒中量表(NIHSS)评分中位数为7(四分位间距,4 - 13)。其中,9465例(11.9%)接受替奈普酶治疗(平均[标准差]年龄,69.6[14.7]岁;NIHSS评分中位数,7[四分位间距,4 - 14];4504例[47.6%]为女性),70085例(88.1%)接受阿替普酶治疗(平均[标准差]年龄,68.5[14.8]岁;NIHSS评分中位数,7[四分位间距,4 - 13];34092例[48.6%]为女性)。在调整协变量后,替奈普酶与阿替普酶在总体队列的疗效或安全性结局方面未发现显著差异,包括出院时功能独立(AOR,1.00;95%CI,0.93 - 1.07)、sICH(AOR,0.96;95%CI,0.83 - 1.11)以及院内死亡或临终关怀出院(AOR,0.98;95%CI,0.89 - 1.07),但在有资格接受但未接受血管内血栓切除术的患者中,出院回家(AOR,1.26;95%CI,1.03 - 1.53)、院内死亡(AOR,0.63;95%CI,0.47 - 0.85)以及院内死亡或临终关怀出院的合并情况(AOR,0.78;95%CI,0.62 - 0.97)方面发现有显著改善。
这项使用常规临床实践数据的大型全国性比较疗效研究表明,急性缺血性卒中患者使用替奈普酶与阿替普酶的疗效和安全性结局相似。本研究支持替奈普酶作为阿替普酶的合理替代药物。