错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

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

  • Ying Li,
  • Qianhua Ou,
  • Yuxuan Lu,
  • Zhiyuan Shen,
  • Jieyu Li,
  • Zhuangzhuang Zhang,
  • Liwen Tai,
  • Guozhong Li,
  • Huisheng Chen,
  • Guiru Zhang,
  • Lei Zhang,
  • Xuwen Sun,
  • Jinhua Qiu,
  • Yan Wei,
  • Sainan Zhu,
  • Zhaoxia Wang,
  • Weiping Sun,
  • Yining Huang

摘要

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).