RESULTS IN TREATMENT AND SAFETY OF LOW-DOSE INTRAVENOUS RECOMBINANT TISSUE PLASMINOGEN ACTIVATOR IN ACUTE ISCHEMIC STROKE WITHOUT LARGE VESSEL OCCLUSION SCREENED BY MRI 3 TESLA
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Abstract
Background: Cerebrovascular disease causes more than 6 million deaths globally. Magnetic resonance imaging (MRI) is better at examining the brain than computed tomography (CT) for acute ischemic stroke (AIS). Alteplase is accepted to treat stroke <4.5 hours, reducing mortality and disability. In addition, low doses of rTPA reduced intracranial bleeding compared with standard doses. However, the efficacy and safety of low-dose use in stroke without large vessel occlusion (LVO) have not been thoroughly evaluated. Objectives: To analyze results and safety of low-dose IV rTPA in AIS without LVO. Materials and methods: This was a cross-sectional study in patients AIS without LVO within 4.5 hours of stroke onset who were treated with low-dose rTPA screened by MRI 3 Tesla. The primary outcome was the good outcome rate at 3 months and safety via rate of intracranial hemorrhage and mortality in 90 days. Results: Between February 2019 and July 2021, there were 92 eligible patients. NIHSS score at admission was 7.5±3.7; at discharge or after 7 days admission was 3.3±3.5. mRS at admission was 2.9±0.8; at 90 days was 1.1± 1.1. There were 3(3.3%) patients with complications relating to treatment with low-dose of rTPA: 1.1% intracranial hemorrhage; 1.1% new infarcts; 1.1% gastrointestinal bleeding; no deaths in 90 days. Conclusions: Our study suggests that the efficacy, safety of low-dose rTPA in AIS without LVO within 4.5 hours. Patient selection for rTPA by MRI 3 Tesla contributed to decrease complication and mortality.
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Keywords
Low-dose intravenous recombinant tissue plasminogen activator, acute ischemic stroke
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