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Geographic differences in pharmacotherapy patterns and outcomes of acute ischemic stroke in China

医学 药物治疗 内科学 改良兰金量表 逻辑回归 冲程(发动机) 溶栓 共病 多元分析 他汀类 神经学 前瞻性队列研究 急诊医学 缺血性中风 缺血 心肌梗塞 工程类 精神科 机械工程
作者
Ying Li,Q. Ou,Yuxuan Lu,Zhiyuan Shen,Jieyu Li,Zhuangzhuang Zhang,Liwen Tai,Guozhong Li,Dawei Chen,Guiru Zhang,Lei Zhang,Xuwen Sun,Jinhua Qiu,Yan Wei,Sainan Zhu,Zhao-xia Wang,Weiping Sun,Yining Huang
出处
期刊:BMC Neurology [Springer Nature]
卷期号:24 (1)
标识
DOI:10.1186/s12883-024-03564-9
摘要

Abstract Background Vast economic and healthcare status discrepancies exist among regions in China, contributing to different treatment patterns. This study was aimed to investigate the current status of pharmacotherapy for acute ischemic stroke (AIS) and outcomes in China and explore the geographic variation in stroke care. Methods This study was a multicenter prospective registry study, which collected the data of patients with AIS from 80 hospitals in 46 cities in 2015–2017 across China. Poor functional outcome defined as a modified Rankin Scale score of 3–6 was assessed at 3 and 12 months. Multivariate logistic regression was used. Results Among 9973 eligible patients, the number of receiving intravenous thrombolysis (IVT), antiplatelet agents, anticoagulants, statin and human urinary kallidinogenase was 429 (4.3%), 9363 (93.9%), 1063 (10.7%), 6828 (74.7%) and 5112 (51.2%), respectively. Multivariable analysis showed IVT use in northeastern was significantly more frequent than in eastern region (OR = 3.17, 95% CI, 2.53–3.99), while the antiplatelets agents use were less frequent (OR = 0.46, 95%CI: 0.38–0.57). The proportions of poor outcomes at 3 and 12 months were 20.7% and 15.8%, respectively. Multivariate analysis showed AIS patients from northeastern and central region had significantly lower risk of poor outcome at month 3 and 12 than those from eastern region (all P < 0.05). Conclusions There was a low IVT use and a high antiplatelet agent and statin use for AIS in China. The pharmacotherapy and prognosis of AIS had variation by geographic region. Trial registration This study was registered with ClinicalTrials.gov (NCT02470624).

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