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Impact of stress hyperglycemia on outcomes in patients with large ischemic stroke

医学 改良兰金量表 缺血性中风 内科学 冲程(发动机) 入射(几何) 糖尿病 前瞻性队列研究 缺血 内分泌学 机械工程 光学 物理 工程类
作者
Xiaolei Shi,Shihai Yang,Changwei Guo,Wenzhe Sun,Jiaxing Song,Shitao Fan,Jie Yang,Chengsong Yue,Jiandi Huang,Linyu Li,Yan Tian,Jinfu Ma,Xu Xu,Zhi‐Xi Wang,Weilin Kong,Dongsheng Ye,Zhouzhou Peng,Fengli Li,Wenjie Zi
出处
期刊:Journal of NeuroInterventional Surgery [BMJ]
卷期号:17 (10): jnis-2024 被引量:4
标识
DOI:10.1136/jnis-2024-021899
摘要

Background Clinical evidence of the potential influence of stress hyperglycemia ratio (SHR) for patients with large ischemic stroke whether or not receiving endovascular therapy is not clear. Methods This study was a subanalysis of a prospective, multicenter registry, and included 745 patients with large ischemic stroke across 38 centers in China. A total of 427 patients were included in this study, with 285 received endovascular therapy (EVT) and 142 received standard medical therapy (SMT). SHR was defined as glucose (mmol/L)/(1.59 × HbA1C)–2.59. The primary outcome was a moderate neurological outcome (modified Rankin Scale (mRS) score ≤3) at 90 days. Results A significant interaction was observed between SHR and whether received EVT (p=0.017). Among patients who received EVT (adjusted OR (aOR) 0.46; 95% CI 0.23 to 0.92; p=0.029), patients in the highest tertile of SHR were significantly less likely to achieve a moderate neurological outcome at 90 days compared with those in the lowest tertile. However, this association was not observed in patients receiving SMT (aOR 2.46; 95% CI 0.74 to 8.21; p=0.142). EVT patients with higher SHR had a significantly higher incidence of symptomatic intracranial hemorrhage compared with lower SHR (aOR 3.29; 95% CI 1.08 to 10.06; p=0.036), while such an association was not observed in the SMT group (aOR 1.52; 95% CI 0.56 to 4.12; p=0.410). Conclusions In patients with large ischemic stroke treated with EVT, SHR is associated with a reduced likelihood of achieving a moderate neurological outcome, as well as an increased risk of symptomatic intracranial hemorrhage. Trial registration number ChiCTR2100051664.
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