Pan Yuesong, Li Zixiao, Li Jiejie, Jin Aoming, Lin Jinxi, Jing Jing, Li Hao, Meng Xia, Wang Yilong, Wang Yongjun
Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
China National Clinical Research Center for Neurological Diseases, Beijing, China.
J Stroke. 2021 Jan;23(1):51-60. doi: 10.5853/jos.2020.03391. Epub 2021 Jan 31.
Despite administration of evidence-based therapies, residual risk of stroke recurrence persists. This study aimed to evaluate the residual risk of recurrent stroke in acute ischemic stroke or transient ischemic attack (TIA) with adherence to guideline-based secondary stroke prevention and identify the risk factors of the residual risk.
Patients with acute ischemic stroke or TIA within 7 hours were enrolled from 169 hospitals in Third China National Stroke Registry (CNSR-III) in China. Adherence to guideline-based secondary stroke prevention was defined as persistently receiving all of the five secondary prevention medications (antithrombotic, antidiabetic and antihypertensive agents, statin and anticoagulants) during hospitalization, at discharge, at 3, 6, and 12 months if eligible. The primary outcome was a new stroke at 12 months.
Among 9,022 included patients (median age 63.0 years and 31.7% female), 3,146 (34.9%) were identified as adherence to guideline-based secondary prevention. Of all, 864 (9.6%) patients had recurrent stroke at 12 months, and the residual risk in patients with adherence to guidelinebased secondary prevention was 8.3%. Compared with those without adherence, patients with adherence to guideline-based secondary prevention had lower rate of recurrent stroke (hazard ratio, 0.85; 95% confidence interval, 0.74 to 0.99; P=0.04) at 12 months. Female, history of stroke, interleukin-6 ≥5.63 ng/L, and relevant intracranial artery stenosis were independent risk factors of the residual risk.
There was still a substantial residual risk of 12-month recurrent stroke even in patients with persistent adherence to guideline-based secondary stroke prevention. Future research should focus on efforts to reduce the residual risk.
尽管采用了循证疗法,但卒中复发的残余风险依然存在。本研究旨在评估急性缺血性卒中或短暂性脑缺血发作(TIA)患者在遵循基于指南的二级卒中预防措施情况下复发性卒中的残余风险,并确定残余风险的危险因素。
从中国国家卒中登记研究三期(CNSR-III)的169家医院纳入发病7小时内的急性缺血性卒中和TIA患者。遵循基于指南的二级卒中预防定义为,如果符合条件,在住院期间、出院时、3个月、6个月和12个月持续服用所有五种二级预防药物(抗血栓药物、抗糖尿病药物、抗高血压药物、他汀类药物和抗凝剂)。主要结局是12个月时发生新的卒中。
在纳入的9022例患者(中位年龄63.0岁,女性占31.7%)中,3146例(34.9%)被确定为遵循基于指南的二级预防。总体而言,864例(9.6%)患者在12个月时发生复发性卒中,遵循基于指南的二级预防患者的残余风险为8.3%。与未遵循者相比,遵循基于指南的二级预防患者在12个月时复发性卒中发生率较低(风险比,0.85;95%置信区间,0.74至0.99;P=0.04)。女性、卒中病史、白细胞介素-6≥5.63 ng/L以及相关颅内动脉狭窄是残余风险的独立危险因素。
即使是持续遵循基于指南的二级卒中预防措施的患者,12个月复发性卒中仍存在相当大的残余风险。未来研究应致力于降低残余风险。