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常压高氧联合基于时变梯度的血管内治疗:剂量递增研究。

Normobaric Hyperoxia Combined With Endovascular Treatment Based on Temporal Gradient: A Dose-Escalation Study.

机构信息

Department of Neurology, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Jinan, China (W.L.).

Beijing Institute of Brain Disorders, Laboratory of Brain Disorders, Ministry of Science and Technology, Collaborative Innovation Center for Brain Disorders (W.L., J.L., M.W., X.J.).

出版信息

Stroke. 2024 Jun;55(6):1468-1476. doi: 10.1161/STROKEAHA.123.046106. Epub 2024 May 15.

Abstract

BACKGROUND

Normobaric hyperoxia (NBO) has neuroprotective effects in acute ischemic stroke. Thus, we aimed to identify the optimal NBO treatment duration combined with endovascular treatment.

METHODS

This is a single-center, randomized controlled, open-label, blinded-end point dose-escalation clinical trial. Patients with acute ischemic stroke who had an indication for endovascular treatment at Tianjin Huanhu Hospital were randomly assigned to 4 groups (1:1 ratio) based on NBO therapy duration: (1) control group (1 L/min oxygen for 4 hours); (2) NBO-2h group (10 L/min for 2 hours); (3) NBO-4h group (10 L/min for 4 hours); and (4) NBO-6h group (10 L/min for 6 hours). The primary outcome was cerebral infarction volume at 72 hours after randomization using an intention-to-treat analysis model. The primary safety outcome was the 90-day mortality rate.

RESULTS

Between June 2022 and September 2023, 100 patients were randomly assigned to the following groups: control group (n=25), NBO-2h group (n=25), NBO-4h group (n=25), and NBO-6h group (n=25). The 72-hour cerebral infarct volumes were 39.4±34.3 mL, 30.6±30.1 mL, 19.7±15.4 mL, and 22.6±22.4 mL, respectively (=0.013). The NBO-4h and NBO-6h groups both showed statistically significant differences (adjusted values: 0.011 and 0.027, respectively) compared with the control group. Compared with the control group, both the NBO-4h and NBO-6h groups showed significant differences (<0.05) in the National Institutes of Health Stroke Scale scores at 24 hours, 72 hours, and 7 days, as well as in the change of the National Institutes of Health Stroke Scale scores from baseline to 24 hours. Additionally, there were no significant differences among the 4 groups in terms of 90-day mortality rate, symptomatic intracranial hemorrhage, early neurological deterioration, or severe adverse events.

CONCLUSIONS

The effectiveness of NBO therapy was associated with oxygen administration duration. Among patients with acute ischemic stroke who underwent endovascular treatment, NBO therapy for 4 and 6 hours was found to be more effective. Larger-scale multicenter studies are needed to validate these findings.

REGISTRATION

URL: https://www.clinicaltrials.gov; Unique identifier: NCT05404373.

摘要

背景

常压高浓度氧(NBO)对急性缺血性脑卒中具有神经保护作用。因此,我们旨在确定与血管内治疗联合应用的最佳 NBO 治疗时间。

方法

这是一项单中心、随机对照、开放标签、盲终点剂量递增临床试验。天津环湖医院符合血管内治疗适应证的急性缺血性脑卒中患者,根据 NBO 治疗时间随机分为 4 组(1:1 比例):(1)对照组(1 L/min 氧气 4 小时);(2)NBO-2h 组(10 L/min 氧气 2 小时);(3)NBO-4h 组(10 L/min 氧气 4 小时);和(4)NBO-6h 组(10 L/min 氧气 6 小时)。主要结局为采用意向治疗分析模型评估随机分组后 72 小时的脑梗死体积。主要安全性结局为 90 天死亡率。

结果

2022 年 6 月至 2023 年 9 月,共纳入 100 例患者,随机分为以下 4 组:对照组(n=25)、NBO-2h 组(n=25)、NBO-4h 组(n=25)和 NBO-6h 组(n=25)。72 小时脑梗死体积分别为 39.4±34.3 mL、30.6±30.1 mL、19.7±15.4 mL 和 22.6±22.4 mL(=0.013)。NBO-4h 和 NBO-6h 组与对照组相比均有统计学意义(校正值分别为 0.011 和 0.027)。与对照组相比,NBO-4h 和 NBO-6h 组在 24 小时、72 小时和 7 天的国立卫生研究院卒中量表评分以及从基线到 24 小时的国立卫生研究院卒中量表评分变化方面均有显著差异(<0.05)。4 组间 90 天死亡率、症状性颅内出血、早期神经功能恶化或严重不良事件发生率无显著差异。

结论

NBO 治疗的效果与吸氧时间有关。在接受血管内治疗的急性缺血性脑卒中患者中,NBO 治疗 4 小时和 6 小时更为有效。需要更大规模的多中心研究来验证这些发现。

登记

网址:https://www.clinicaltrials.gov;唯一标识符:NCT05404373。

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