Department of Neurology, General Hospital of Northern Theater Command, Shenyang, 110016, China.
Department of Neurology, Anshan Changda Hospital, Anshan, 114000, China.
Nat Commun. 2023 May 5;14(1):2592. doi: 10.1038/s41467-023-38313-y.
We aim to explore the effect of head-down position (HDP), initiated within 24 hours of onset, in moderate anterior circulation stroke patients with probable large artery atherosclerosis (LAA) etiology. This investigator-initiated, multi-center trial prospective, randomized, open-label, blinded-endpoint, multi-center and phase-2 trial was conducted in China and completed in 2021. Eligible patients were randomly assigned (1:1) into the HDP group receiving -20° Trendelenburg, or control group receiving standard care according to national guideline. The primary endpoint was proportion of modified Rankin Scale (mRS) of 0 to 2 at 90 days, which is a scale for measuring the degree of disability after stroke. 90-day mRS was assessed by a certified staff member who was blinded to group assignment. A total of 96 patients were randomized (47 in HDP group and 49 in control group) and 94 (97.9%) patients were included in the final analysis: 46 in HDP group and 48 in control group. The proportion of favorable outcome was 65.2% (30/46) in the HDP group versus 50.0% (24/48) in the control group (unadjusted: OR 2.05 [95%CI 0.87-4.82], P = 0.099). No severe adverse event was attributed to HDP procedures. This work suggests that the head-down position seems safe and feasible, but does not improve favorable functional outcome in acute moderate stroke patients with LAA. This trial was registered with ClinicalTrials.gov, NCT03744533.
我们旨在探讨在可能由大动脉粥样硬化(LAA)引起的中等前循环卒中患者中,于发病后 24 小时内开始采取头低位(HDP)的效果。这是一项由研究者发起的、多中心、前瞻性、随机、开放标签、盲终点、多中心和 2 期试验,在中国进行,于 2021 年完成。符合条件的患者被随机分配(1:1)进入 HDP 组(接受-20°特伦德伦伯格卧位)或对照组(根据国家指南接受标准护理)。主要终点是 90 天时改良 Rankin 量表(mRS)评分 0-2 的比例,这是一种衡量卒中后残疾程度的量表。90 天 mRS 由一名经过认证的工作人员进行评估,该工作人员对分组分配情况不知情。共有 96 名患者被随机分配(HDP 组 47 例,对照组 49 例),94 名(97.9%)患者纳入最终分析:HDP 组 46 例,对照组 48 例。HDP 组的良好结局比例为 65.2%(30/46),对照组为 50.0%(24/48)(未调整:OR 2.05[95%CI 0.87-4.82],P=0.099)。没有严重的不良事件归因于 HDP 程序。这项工作表明,头低位似乎是安全可行的,但不能改善 LAA 急性中度卒中患者的良好功能结局。这项试验在 ClinicalTrials.gov 上注册,编号为 NCT03744533。