医学
镇静
冲程(发动机)
血管内治疗
麻醉
观察研究
循环(流体动力学)
急性中风
外科
缺血性中风
心脏病学
内科学
急诊科
缺血
精神科
工程类
动脉瘤
物理
热力学
机械工程
作者
Fa Liang,Youxuan Wu,Xinyan Wang,Yan Li,Song Zhang,Minyu Jian,Haiyang Liu,Anxin Wang,Fan Wang,Ruquan Han,Matthew T.V. Chan,Zhongrong Miao,Xiaochuan Huo,Yuming Peng,Guoming Li,Yang Zhou,Yang Bai,Xiuheng Li,Xiang Yan,Wanning Yang
出处
期刊:JAMA Neurology
[American Medical Association]
日期:2022-09-26
卷期号:80 (1): 64-64
被引量:40
标识
DOI:10.1001/jamaneurol.2022.3018
摘要
No definitive conclusion can be made on the best choice of anesthesia for people with acute posterior circulation stroke during endovascular treatment. Only a few observational studies have focused on this topic in recent years, and they have differing conclusions. To examine whether conscious sedation (CS) is a feasible alternative to general anesthesia (GA) during endovascular treatment in patients with acute posterior circulation stroke. A randomized parallel-group exploratory trial with blinded end point evaluation (Choice of Anesthesia for Endovascular Treatment of Acute Ischemic Stroke [CANVAS II]) enrolled adult patients from March 2018 to June 2021 at 2 comprehensive care hospitals in China. Patients with acute posterior circulation stroke were enrolled, randomized, and monitored for 3 months. Of 210 patients admitted with acute ischemic posterior circulation stroke, 93 were recruited and 87 were included in the intention-to-treat (ITT) analysis after exclusions, 43 were assigned to GA and 44 to CS. All analyses were unadjusted or adjusted with the ITT principle. Participants were randomly assigned to CS or GA in a 1:1 ratio. The primary end point was functional independence at 90 days evaluated with the modified Rankin Scale (mRS). A total of 87 participants were included in the ITT study (mean [SD] age, 62 [12] years; 16 [18.4%] female and 71 [81.6%] male). Of these, 43 were in the GA group and 44 in the CS group. The overall baseline median (IQR) National Institute of Health Stroke Scale (NIHSS) score was 15 (12-17). In the CS group, 13 people (29.5%) were ultimately transferred to GA. The CS group had a higher incidence of functional independence; however, no significant difference was found between the 2 groups (48.8% vs 54.5%; risk ratio, 0.89; 95% CI, 0.58-1.38; adjusted odds ratio [OR], 0.91; 95% CI, 0.37-2.22). However, GA performed better in successful reperfusion (mTICI 2b-3) under ITT analysis (95.3% vs 77.3%; adjusted OR, 5.86; 95% CI, 1.16-29.53). The findings in this study suggest that CS was not better than GA for the primary outcome of functional recovery and was perhaps worse for the secondary outcome of successful reperfusion. ClinicalTrials.gov Identifier: NCT03317535.
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