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首页> 外文期刊>Neurological Research: An Interdisciplinary Quarterly Journal >Percutaneous mastoid electrical stimulator alleviates autonomic dysfunction in patients with acute ischemic stroke
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Percutaneous mastoid electrical stimulator alleviates autonomic dysfunction in patients with acute ischemic stroke

机译:经皮乳突电刺激器减轻了急性缺血性卒中患者的自主功能障碍

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Background and Purpose: Poststroke prognosis is associated with autonomic status. The purpose of our study was to determine whether percutaneous mastoid electrical stimulator (PMES) can alleviate abnormal heart rate variability (HRV) and improve clinical outcome. Methods: This prospective, randomized, double-blinded, placebo-controlled study enrolled a total of 140 patients with autonomic dysfunction within 3d after acute ischemic stroke. The patients were treated with PMES or sham stimulation once daily over a period of 2 weeks. HRV was primarily assessed by the fractal dimension (FD) at admission and 2 weeks. All patients were followed up for 3 months. The clinical outcome was death and major disability (modified Rankin Scale score = 3) at 3 months after acute ischemic stroke. Results: FD of the 2-week treatment period increased in PMES groups. PMES can significantly alleviate abnormal HRV. The difference in FD of the 2-week treatment period between the PMES and sham groups was significant (1.14 +/- 0.27 vs. 1.00 +/- 0.23; P = 0.001). In fully adjusted models, PMES was associated with reduced 3-month mortality (adjusted odds ratio, 0.32; 95% confidence interval, 0.11-0.93; P = 0.036). No significant group differences were seen in three major disability and composite outcome (P 0.05). Conclusions: PMES was a safe, effective, and low-cost therapy to alleviate HRV and could significantly reduce mortality in the early recovery phase after acute ischemic stroke.
机译:背景和目的:预后预后与自主状态有关。我们研究的目的是确定经皮乳突电刺激器(PMES)是否可以缓解异常心率变异性(HRV)并改善临床结果。方法:此前瞻性,随机,双盲,安慰剂对照研究总共注册了140例急性缺血性卒中后3D内的自主功能障碍。每天在2周内每天用PME或假刺激治疗患者。 HRV主要由入院和2周的分形维数(FD)进行评估。所有患者均进行3个月。急性缺血性卒中后3个月,临床结果是死亡和重大残疾(修改Rankin Scade& 3)。结果:PMES组的2周治疗期的FD增加。 PME可以显着减轻异常HRV。 PMES和假组之间的2周治疗时间的FD的差异很大(1.14 +/- 0.27与1.00 +/- 0.23; p = 0.001)。在完全调整的模型中,PME与3个月的死亡率降低有关(调整的差距,0.32; 95%置信区间,0.11-0.93; p = 0.036)。在三个主要的残疾和复合结果中没有看到显着的群体差异(P> 0.05)。结论:PMES是一种安全,有效,低成本的治疗,可缓解HRV,可显着降低急性缺血性卒中后早期回收阶段的死亡率。

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