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Intravenous thrombolysis in acute mild non-disabling ischemic stroke: A retrospective cohort study.

Source: PubMed, NCBI / U.S. National Library of Medicine

The American journal of emergency medicineLei Junjie, Cai Yiming, Liu Xudong, et al.Published 6/3/2026Last synced 6/10/2026Status: syncedPMID: 42263336DOI: 10.1016/j.ajem.2026.06.008

The benefit of intravenous thrombolysis (IVT) in patients with acute mild, non-disabling ischemic stroke remains uncertain. We evaluated the real-world effectiveness and safety of IVT and explored heterogeneity of treatment effects in prespecified subgroups. We conducted a single-center retrospective observational cohort study of consecutive adults with acute mild, non-disabling ischemic stroke treated at the Stroke Center of the Fifth Affiliated Hospital of Sun Yat-sen University (March 2019-October 2023). Eligible patients presented within 6 h, had baseline NIHSS ≤ 5 with each item ≤ 1 (and 0 on consciousness items), and had no deficits perceived as potentially disabling. Patients receiving endovascular therapy after IVT or scheduled cerebrovascular intervention within 3 months were excluded. The primary outcome was excellent functional outcome (90-day mRS 0-1). Secondary outcomes were functional independence (90-day mRS 0-2) and early neurological deterioration (END; NIHSS increase>2 within 7 days). Safety outcomes included hemorrhagic transformation (HT) and symptomatic intracranial hemorrhage (sICH). Group comparisons used standard univariable tests; prespecified subgroup analyses were performed. Among 228 patients (mean age 60.7 ± 12.5 years; 66.3% male), 185 received IVT and 43 did not. Baseline characteristics were similar, except for a slightly higher median admission NIHSS in the IVT group (2 [IQR

Abstract

The benefit of intravenous thrombolysis (IVT) in patients with acute mild, non-disabling ischemic stroke remains uncertain. We evaluated the real-world effectiveness and safety of IVT and explored heterogeneity of treatment effects in prespecified subgroups. We conducted a single-center retrospective observational cohort study of consecutive adults with acute mild, non-disabling ischemic stroke treated at the Stroke Center of the Fifth Affiliated Hospital of Sun Yat-sen University (March 2019-October 2023). Eligible patients presented within 6&#xa0;h, had baseline NIHSS&#xa0;&#x2264;&#xa0;5 with each item&#xa0;&#x2264;&#xa0;1 (and 0 on consciousness items), and had no deficits perceived as potentially disabling. Patients receiving endovascular therapy after IVT or scheduled cerebrovascular intervention within 3&#xa0;months were excluded. The primary outcome was excellent functional outcome (90-day mRS 0-1). Secondary outcomes were functional independence (90-day mRS 0-2) and early neurological deterioration (END; NIHSS increase>2 within 7&#xa0;days). Safety outcomes included hemorrhagic transformation (HT) and symptomatic intracranial hemorrhage (sICH). Group comparisons used standard univariable tests; prespecified subgroup analyses were performed. Among 228 patients (mean age 60.7&#xa0;&#xb1;&#xa0;12.5&#xa0;years; 66.3% male), 185 received IVT and 43 did not. Baseline characteristics were similar, except for a slightly higher median admission NIHSS in the IVT group (2 [IQR 1-2] vs 1 [IQR 1-2]; P&#xa0;<&#xa0;0.001). At 90&#xa0;days, mRS 0-1 occurred in 84.9% with IVT versus 74.4% without IVT (P&#xa0;=&#xa0;0.117); functional independence (mRS&#xa0;&#x2264;&#xa0;2) was 94.1% vs 90.7% (P&#xa0;=&#xa0;0.492). END occurred in 12.4% vs 25.6% (P&#xa0;=&#xa0;0.054). Any HT occurred in 5.9% vs 4.7% (P&#xa0;=&#xa0;0.542); sICH was rare (1.1% vs 0.0%; P&#xa0;=&#xa0;0.658). Subgroup analyses suggested a potential benefit of IVT in patients aged&#xa0;&#x2265;&#xa0;65&#xa0;years for achieving mRS 0-1. In acute mild, non-disabling ischemic stroke, IVT was not associated with increased hemorrhagic complications and did not significantly improve overall 90-day excellent functional outcome. Patients aged&#xa0;&#x2265;&#xa0;65&#xa0;years may derive greater functional benefit from IVT, warranting confirmation in larger prospective studies.

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