Trajectories of stroke severity and functional outcomes after endovascular treatment in ischemic stroke: A post hoc analysis of a randomized controlled trial

医学 冲程(发动机) 优势比 置信区间 随机对照试验 析因分析 逻辑回归 内科学 物理疗法 疾病严重程度 机械工程 工程类
作者
Shuxian Huo,Jie Gao,Qiushi Lv,Mengdi Xie,Huaiming Wang,Xiaohao Zhang,Yi Xie,Min Wu,Rui Liu,Xinfeng Liu,Kang Yuan,Ruidong Ye
出处
期刊:Clinical Neurology and Neurosurgery [Elsevier BV]
卷期号:239: 108248-108248 被引量:4
标识
DOI:10.1016/j.clineuro.2024.108248
摘要

The trajectory of early neurological changes in patients with acute ischemic stroke has been understudied. This study aimed to investigate the association between longitudinal trajectories of stroke severity and 90-day functional outcomes in patients with acute ischemic stroke receiving endovascular treatment. We enrolled patients from a prospective, multicenter, randomized controlled trial. The stroke severity was assessed with the National Institute of Health Stroke Scale at the pre-procedure, 24 hours, and seven days after the procedure. Group-based trajectory modeling (GBTM) was used to identify trajectories of stroke severity. Multivariable logistic regression was performed to explore the association between stroke severity markers and 90-day functional outcomes. Of 218 enrolled patients, 127 (58.3%) had poor functional outcomes at 90 days. We identified three trajectories of stroke severity in the GBTM: stable symptom (38.1%), symptom deterioration (17.0%), and symptom improvement (44.9%). In multivariable analyses, trajectories of stroke severity were associated with an increased risk of poor functional outcomes (symptom improvement versus symptom deterioration: odds ratio, 0.007; 95% confidence interval, 0.001–0.040; P <0.001). Reclassification indexes revealed that trajectories of stroke severity would increase the predictive ability for poor functional outcomes at 90 days. After endovascular treatment, patients would follow one of three distinct trajectories of stroke severity. Symptom deterioration trajectory was associated with an increased risk of poor functional outcomes at 90 days. NCT04973332.
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