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        <identifier>oai:figshare.com:article/33992008</identifier>
        <datestamp>2026-09-25T04:25:18Z</datestamp>
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          <dc:title>Supplementary file 1_Tenecteplase versus alteplase for intravenous thrombolysis in acute ischemic stroke: a single-center propensity-weighted cohort study.docx</dc:title>
          <dc:creator>Jin Ma (335456)</dc:creator>
          <dc:creator>Heyireguli Wulayimu (25107010)</dc:creator>
          <dc:creator>Zhiqiang Ma (127376)</dc:creator>
          <dc:subject>Neurology and Neuromuscular Diseases</dc:subject>
          <dc:subject>acute ischemic stroke</dc:subject>
          <dc:subject>alteplase</dc:subject>
          <dc:subject>functional outcome</dc:subject>
          <dc:subject>intravenous thrombolysis</dc:subject>
          <dc:subject>inverse probability of treatment weighting</dc:subject>
          <dc:subject>tenecteplase</dc:subject>
          <dc:description>Background&lt;p&gt;Tenecteplase can be given as a single bolus, but comparative estimates from routine stroke care are susceptible to treatment-selection bias. Methods: We reviewed 269 adults treated at one center with intravenous tenecteplase (n = 110) or alteplase (n = 159) within 4.5 h of symptom onset from March 2024 through March 2026. The primary outcome was functional independence at 90 days [modified Rankin Scale (mRS) 0–2]. A logistic propensity-score model included pretreatment clinical and laboratory variables. Stabilized average-treatment-effect weights were truncated at the 1st and 99th percentiles. We report weighted risks, risk differences (RDs), odds ratios (ORs), and robust 95% confidence intervals (CIs). Secondary neurological/workflow and safety outcomes were adjusted within separate families using the Holm procedure.&lt;/p&gt;Results&lt;p&gt;After weighting, 90-day functional independence was 77.9% with tenecteplase and 81.3% with alteplase (RD, −3.5 percentage points; 95% CI, −17.0 to 10.1; p = 0.616; OR, 0.81; 95% CI, 0.36–1.82). Holm-adjusted p values for the other functional outcomes were 1.000. The weighted mean difference in door-to-needle time was −5.0 min (95% CI, −9.0 to −0.9; unadjusted p = 0.017; Holm-adjusted p = 0.068). Day-7 early neurological deterioration occurred in no tenecteplase recipient and nine alteplase recipients (weighted RD, −5.1 percentage points; 95% CI, −8.5 to −1.7; Holm-adjusted p = 0.016). SITS-MOST symptomatic intracranial hemorrhage occurred in four patients, with a weighted RD of 0.2 percentage points (95% CI, −1.7 to 2.1).&lt;/p&gt;Conclusion&lt;p&gt;Tenecteplase was not associated with greater 90-day functional independence in this propensity-weighted cohort. No clear between-group difference was observed in major hemorrhagic outcomes. DNT was shorter before multiplicity adjustment, and day-7 deterioration was less frequent after adjustment within the secondary neurological/workflow family.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-25T04:25:18Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fneur.2026.1928004.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Supplementary_file_1_Tenecteplase_versus_alteplase_for_intravenous_thrombolysis_in_acute_ischemic_stroke_a_single-center_propensity-weighted_cohort_study_docx/33992008</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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