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May 8, 2026European Stroke Journal0 citations

Abstract Number: Esoc2026a2290 Intra-Arterial Thrombolytics After Endovascular Thrombectomy for Acute Ischemic Stroke: A Network Meta-Analysis of Randomized Controlled Trials

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AAAbdallah AbbasMEMohamed ElfilHSHaneen Sabet

Key Points

  • This analysis assesses the efficacy and safety of intra-arterial thrombolysis after successful endovascular thrombectomy for acute ischemic stroke due to large vessel occlusion.
  • Systematic review and network meta-analysis of randomized controlled trials comparing IAT versus EVT alone.
  • Included seven trials with a total of 2,131 patients to evaluate primary and safety outcomes related to IAT.
  • Primary outcomes included 90-day modified Rankin Scale and mortality; safety outcomes focused on intracranial hemorrhage.
  • EVT + TNK 0.125 mg/kg resulted in mRS 0-1 improvement (RR 1.54, 95% CI 1.07–2.20) compared to EVT alone.
  • EVT + ALT 0.225 mg/kg also improved mRS 0-1 (RR 1.48, 95% CI 1.17–1.86) versus EVT.
  • EVT + TNK 0.0625 mg/kg increased risk of any intracranial hemorrhage (RR 1.34, 95% CI 1.08–1.66), but not symptoms.

Abstract

Abstract Background and aims Endovascular thrombectomy (EVT) is the gold standard treatment for acute ischemic stroke (AIS) caused by large vessel occlusion (LVO) in patients meeting certain eligibility criteria. A critical challenge in this regard is the phenomenon of futile recanalization, which can be partially explained by embolism of the distal microcirculation. Thus, a few clinical trials investigated the efficacy and safety profile of intra-arterial thrombolysis (IAT) post successful EVT, aiming to improve EVT’s clinical outcomes without increasing the risk of hemorrhagic complications. We aim to evaluate the efficacy and safety of adjunctive IAT after successful EVT for AIS-LVO. Methods A systematic review and network meta-analysis (NMA) of randomized controlled trials comparing IAT (alteplase (ALT), tenecteplase (TNK), or urokinase (UK)) versus EVT alone were conducted. Primary outcomes were 90-day modified Rankin Scale (mRS) 0–1, mRS 0–2, and mortality; safety outcomes included any and symptomatic intracranial hemorrhage (ICH and sICH). Results Seven trials (2,131 patients) were included. EVT + TNK 0.125 mg/kg (RR 1.54, 95% CI 1.07–2.20) and EVT + ALT 0.225 mg/kg (RR 1.48, 95% CI 1.17–1.86) improved excellent outcomes (mRS 0–1) versus EVT alone. No regimen improved mRS 0–2 or mortality. EVT + TNK 0.0625 mg/kg increased the risk of any ICH (RR 1.34, 95% CI 1.08–1.66), but not the risk of sICH. Conclusions IAT, particularly with ALT 0.225 mg/kg or TNK 0.125 mg/kg, may enhance post-EVT recovery without increasing sICH risk. Larger trials are needed to confirm optimal dosing and patient selection. Conflict of interest All authors have nothing to disclose. Figure 1 - belongs to Methods Table 1 - belongs to Results Figure 1 - belongs to Conclusions

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Cite This Study

Abbas et al. (2026) studied this question.

synapsesocial.com/papers/69fd8021bfa21ec5bbf087abhttps://doi.org/10.1093/esj/aakag023.1053
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