医学
溶栓
随机对照试验
优势比
子群分析
冲程(发动机)
混淆
内科学
逻辑回归
纤溶剂
外科
心脏病学
置信区间
组织纤溶酶原激活剂
心肌梗塞
工程类
机械工程
作者
Gisele Sampaio Silva,Maramelia Miranda Alves,Felipe Chaves Duarte Barros,Michel Eli Frudit,Octávio M. Pontes-Neto,F. Mont’alverne,Letícia C Rebello,Leonardo Augusto Carbonera,Daniel Giansante Abud,Fabrício Oliveira Lima,Ana Cláudia de Souza,David S Liebeskind,Gabriel Mosmann,Daniel C. Bezerra,Jeffrey L. Saver,Fabrício Buchdid Cardoso,Raul G Nogueira,Sheila Martins
标识
DOI:10.1016/j.jns.2023.122853
摘要
Randomized trials have recently evaluated the non-inferiority of direct thrombectomy versus intravenous thrombolysis (IVT) followed by endovascular therapy in anterior circulation large vessel occlusion (LVO) stroke in patients eligible for IVT within 4.5 h from stroke onset with controversial results. We aimed to assess the effect of IVT on the clinical outcome of mechanical thrombectomy (MT) in the RESILIENT trial.RESILIENT was a randomized, prospective, multicenter, controlled trial assessing the safety and efficacy of thrombectomy versus medical treatment alone. A total of 221 patients were enrolled. The trial showed a substantial benefit of MT when added to medical management. All eligible patients received intravenous tPA within the 4.5-h-window. Ordinal logistic and binary regression analyses using intravenous tPA as an interaction term were performed with adjustments for potential confounders, including age, baseline NIHSS score, occlusion site, and ASPECTS. A p-value <0.05 was considered statistically significant.Among 221 randomized patients (median NIHSS, 18 IQR [14-21]), 155 (70%) were treated with IVT. There was no difference in the mRS ordinal shift and frequency of functional independence between patients who received or not IV tPA; the odds ratio for the ordinal mRS shift was 2.63 [1.48-4.69] for the IVT group and 1.54 [0.63-3.74] for the no IVT group, with a p-value of 0.42. IVT also did not affect the frequency of good recanalization (TICI 2b or higher) and hemorrhagic transformation.The large effect size of MT on LVO outcomes was not significantly affected by IVT.RESILIENT ClinicalTrials.gov number, NCT02216643.
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