医学
溶栓
改良兰金量表
优势比
冲程(发动机)
置信区间
脑出血
内科学
轻微中风
缺血性中风
心肌梗塞
缺血
蛛网膜下腔出血
机械工程
狭窄
工程类
作者
Chunmiao Duan,Yunyun Xiong,Hongqiu Gu,Shang Wang,Kaixuan Yang,Manjun Hao,Xingquan Zhao,Xia Meng,Yongjun Wang
摘要
Abstract Aims Our study aimed to describe the short‐, medium‐, and long‐term outcomes of intravenous thrombolysis in minor stroke, and to explore the relationship between thrombolysis and clinical outcomes. Methods Our study included ischemic minor stroke patients (National Institutes of Health Stroke Scale score ≤ 5) within 4.5 h from symptom onset from the Third China National Stroke Registry (CNSR‐III) between August 2015 and March 2018. The primary outcome was a favorable functional outcome, defined as a modified Rankin Scale (mRS) score of 0–1 at 3 months. The secondary outcomes included mRS score of 0–1 at discharge, 6 months, and 1 year. The safety outcomes were symptomatic intracerebral hemorrhage (sICH) at 24–36 h and all‐cause mortality. The association between intravenous thrombolysis and clinical outcomes was studied using multivariable models. Results A total of 1905 minor ischemic stroke patients were included. Overall 527 patients (28%) received intravenous t‐PA (IV t‐PA) and 1378 patients (72%) in the non‐IV t‐PA group. Of them, 18.85% (359/1905) participants had a disabled outcome (defined as mRS score ≥ 2) at discharge, 12.8% (242/1885) at 3 months, 13.9% (262/1886) at 6 months, and 13.9% (260/1871) at 1 year. In multivariable analysis, IV t‐PA was associated with favorable functional outcomes at discharge (adjusted odds ratio [aOR] 1.49; 95% confidence interval [CI] 1.13–1.96; p = 0.004), 3 months (aOR 1.51; 95% CI 1.09–2.10; p = 0.01), 6 months (aOR 1.64; 95% CI 1.19–2.27; p = 0.003), and 1 year (aOR 1.52; 95% CI 1.10–2.10; p = 0.01). Symptomatic ICH occurred in 3 (0.6%) patients in IV t‐PA versus 2 (0.1%) in the non‐IV t‐PA group. No significant differences were found in all‐cause mortality between the two groups. Conclusions Intravenous t‐PA may be safe and effective in minor stroke (NIHSS ≤ 5) within a 4.5‐h window and further randomized controlled trials are warranted.
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