文献速递脑血管病

TEMPO-2亚组:80岁以上轻微卒中替奈普酶溶栓结局更差

Outcomes After Minor Ischemic Stroke in Older Patients Treated With IV Thrombolysis vs Standard of Care in the TEMPO-2 Trial.
PubMed 文献 · Neurology · 2026-04-14

该研究为TEMPO-2随机试验的事后分析,纳入884例轻微卒中伴症状性颅内闭塞或灌注缺损患者,比较替奈普酶与无溶栓标准治疗。80岁以上患者接受替奈普酶后90天mRS 0-1比例更低(46.2% vs 59.8%,aRR 0.83,95%CI 0.72-0.97),严重不良事件更多(RR 2.29,95%CI 1.27-4.13),尽管血管再通和短期神经恢复更优。

要点

  • 80岁以上轻微卒中伴闭塞者,替奈普酶组90天功能独立比例显著低于标准治疗。
  • 替奈普酶在80岁以上组严重不良事件增加,尤其是出血和卒中进展/复发。
  • 两年龄组替奈普酶均提高血管再通率和5天/出院时NIHSS=0比例。

核心结论

  • 80岁以上轻微卒中伴可见闭塞或灌注缺损患者,替奈普酶溶栓与90天功能结局更差相关,不支持该人群溶栓。

研究设计与样本

  • TEMPO-2随机对照试验的事后分析,纳入884例轻微卒中伴症状性颅内闭塞或局灶灌注缺损且症状发作12小时内患者,其中208例(23.5%)>80岁,365例(41.6%)女性。

主要发现

  • >80岁患者中,替奈普酶组mRS 0-1为49例(46.2%),标准治疗组为61例(59.8%),aRR 0.83(95%CI 0.72-0.97)。
  • ≤80岁患者中,替奈普酶组与标准治疗组mRS 0-1无显著差异(249例[76.4%] vs 260例[74.7%],aRR 1.01,95%CI 0.98-1.03)。
  • 两年龄组替奈普酶均提高血管再通率(≤80岁aRR 2.06,95%CI 1.60-2.65;>80岁aRR 2.77,95%CI 2.21-3.47)。
  • 两年龄组替奈普酶均提高5天/出院时NIHSS=0比例(≤80岁aRR 1.14,95%CI 1.04-1.26;>80岁aRR 1.21,95%CI 1.10-1.33)。
  • >80岁患者中替奈普酶组严重不良事件更常见(RR 2.29,95%CI 1.27-4.13),任何颅内外出血为5例(4.7%) vs 0例(p=0.026)。

关键数值与推荐

  • 主要结局为90天mRS应答分析:病前mRS 0-1者应答为mRS 0-1,病前mRS 2者应答为mRS 0-2。
  • 次要结局包括5天/出院时NIHSS神经恢复、血管再通、Lawton工具性日常生活活动量表、EQ-5D和不良事件。

临床怎么用

  • 对80岁以上轻微卒中伴可见闭塞或灌注缺损患者,选择替奈普酶溶栓需谨慎权衡功能获益与出血及卒中进展风险。

局限性

  • 该分析为TEMPO-2试验的事后分析,证据等级为Class III。

以上解读依据论文摘要(全文未开放获取或许可不允许翻译转载)。

原文

BACKGROUND AND OBJECTIVES: There are few high-quality data on thrombolysis outcomes in the oldest patients, especially for minor stroke. We examined safety and efficacy outcomes of thrombolysis in patients older than 80 years, compared with those ≤80 years, in the Tenecteplase Versus Standard of care for Minor Ischaemic Stroke With Proven Occlusion (TEMPO-2) trial. METHODS: In this post hoc analysis of the TEMPO-2 randomized controlled trial, we compared outcomes and adverse events in patients with minor stroke and symptomatic intracranial occlusion or focal perfusion lesion within 12 hours of symptom onset, assigned to tenecteplase vs nonthrombolytic standard of care, in those >80 years and ≤80 years. The primary outcome was responder analysis of the 90-day modified Rankin Scale (responder was mRS = 0-1 if premorbid mRS = 0-1, 0-2 if premorbid mRS = 2). Secondary outcomes included neurologic recovery according to the NIH Stroke Scale (NIHSS) at 5 days/discharge, vessel recanalization, Lawton Instrumental Activities of Daily Living Scale, EuroQol-5 Dimension (EQ-5D), and adverse events. We used mixed-effects Poisson, ordinal logistic, and quantile regression as appropriate, adjusted for sex, baseline NIHSS, and treatment assignment as fixed-effects and enrolling site as random effects. RESULTS: Among 884 patients in the intention-to-treat analysis (208 [23.5%] >80 years, 365 [41.6%] female). Significant interactions between age and treatment were observed for mRS responder, mRS 0-1, return to baseline function, EQ-5D index, and vessel recanalization. Patients >80 years generally fared worse with tenecteplase for mRS outcomes (mRS 0-1 in 49 [46.2%] vs 61 [59.8%] with control, adjusted risk ratio [aRR] 0.83, 95% CI 0.72-0.97), while among patients ≤80 years, there was no significant difference (249 [76.4%] vs 260 [74.7%], aRR 1.01, 95% CI 0.98-1.03). However, in both age groups, patients were more likely to achieve recanalization of visible occlusions (aRR ≤80 years 2.06, 95% CI 1.60-2.65, >80 years 2.77, 95% CI 2.21-3.47) and NIHSS = 0 at 5 days/discharge when assigned to tenecteplase (aRR ≤80 years 1.14, 95% CI 1.04-1.26, >80 years 1.21, 95% CI 1.10-1.33). Serious adverse events (SAEs) were more frequent with tenecteplase among patients >80 years (risk ratio 2.29, 95% CI 1.27-4.13), particularly hemorrhages and stroke progression/recurrence (any extra/intracranial hemorrhage in 5 [4.7%] vs 0 with standard of care, p = 0.026). DISCUSSION: Older patients (>80 years) with minor stroke and visible occlusion or perfusion lesion assigned to tenecteplase were more likely to achieve recanalization of occlusions and short-term neurologic recovery, as were younger patients, but they experienced worse 90-day outcomes with more frequent hemorrhagic and stroke progression/recurrence-related SAEs. Overall, these results, while post hoc, do not support thrombolysis for minor strokes in older patients. TRIAL REGISTRATION INFORMATION: ClinicalTrials.gov: NCT02398656. CLASSIFICATION OF EVIDENCE: This study provides Class III evidence that in patients >80 years with minor stroke and visible occlusion or perfusion lesion, IV thrombolysis with tenecteplase is associated with worse functional outcomes at 90 days compared with nonthrombolytic standard of care therapies.

来源:Neurology,查看原文。版权归原作者所有。

引用

  1. Ganesh A, Vatanpour S, Yu AYX, et al. Outcomes After Minor Ischemic Stroke in Older Patients Treated With IV Thrombolysis vs Standard of Care in the TEMPO-2 Trial. Neurology. 2026. PMID: 41980227. doi:10.1212/WNL.0000000000214925

供执业医师工作参考,不替代临床判断;数值与分级以指南原文为准。