缺氧后口腔自动性的电临床特征和预后意义:一个病例系列和文献回顾。

IF 3.2 Q3 CLINICAL NEUROLOGY
Neurology. Clinical practice Pub Date : 2025-12-01 Epub Date: 2025-09-17 DOI:10.1212/CPJ.0000000000200547
Margil Ranpariya, Osman Farooq, Robert L Glover, Natasha Qutab, Jonathan Hanson, Alexus Ludwig, Ping Li
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引用次数: 0

摘要

背景和目的:缺氧后肌阵挛是心脏骤停后常见的一种现象,通常预后较差。其他自发运动,如强直性眼睑张开,也有记录,但自发咀嚼运动仍然缺乏特征。本研究的目的是系统分析缺氧后咀嚼运动的电生理特征,提出标准化的命名法,讨论潜在的病理生理,并评估其预后意义。方法:我们回顾性回顾了2021年1月至2024年12月期间在连续视频脑电图(vEEG)监测中表现出可疑咀嚼运动的心脏骤停后患者的临床数据。分析咀嚼运动的持续时间、频率以及与脑电图结果的相关性。还收集了人口统计学、临床、管理和结局数据。进行了全面的文献综述。结果:12例院外心脏骤停患者(平均年龄:62.3±10.5岁)出现重复咀嚼动作。视频记录的详细分析和床边观察表明,这些动作是舌头有节奏地抬高上腭,下颌活动最小,在脑电图上产生咀嚼伪影。这些发作持续4-5秒,2例为周期性发作。视频脑电图显示,8例患者的运动在脑电图爆发后1-1.5秒发生,而4例患者的运动是自发发生的,没有相应的皮层活动。这些运动是短暂的,平均持续时间为24小时,尽管持续的爆发抑制模式,但在72小时内消退。3例脑MRI表现为弥漫性缺氧/缺氧皮质损伤,脑干相对保存。所有患者均死于心脏骤停,中位生存期为5天。讨论:我们提出“缺氧后口腔自动性”(PAOA)一词来描述心脏骤停后昏迷患者的一种独特的、短暂的口腔运动现象,其特征是重复的、咀嚼样的舌头运动。与以往的报道不同,我们的研究结果表明,PAOA可以发生在突发抑制和背景抑制的脑电图背景中。这些运动可能是由于负责节律性口面部活动的脑干中枢模式发生器的抑制解除,可能表明严重的皮质功能障碍。虽然PAOA与预后不良相关,但其独立预测价值尚不清楚。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electroclinical Characteristics and Prognostic Significance of Postanoxic Oral Automatism: A Case Series and Literature Review.

Background and objectives: Postanoxic myoclonus is a well-recognized phenomenon after cardiac arrest and often indicates poor prognosis. Other spontaneous movements, such as tonic eyelid opening, have also been documented, but spontaneous chewing movements remain poorly characterized. The aim of this study was to systematically analyze the electrophysiologic features of postanoxic chewing movements, propose a standardized nomenclature, discuss potential pathophysiology, and evaluate their prognostic significance.

Methods: We retrospectively reviewed clinical data from post-cardiac arrest patients who exhibited suspicious chewing movements during continuous video-EEG (vEEG) monitoring between January 2021 and December 2024. Chewing movements were analyzed for duration, frequency, and correlation with EEG findings. Demographic, clinical, management, and outcome data were also collected. A thorough literature review was conducted.

Results: Twelve patients (mean age: 62.3 ± 10.5 years) who experienced out-of-hospital cardiac arrest exhibited repetitive chewing movements. Detailed analysis of video recordings and bedside observations identified these movements as rhythmic tongue elevations against the upper palate with minimal jaw activity, producing chewing artifacts on EEG. These episodes lasted 4-5 seconds and were periodic in 2 patients. Video-EEG revealed that in 8 patients, the movements followed EEG bursts by 1-1.5 seconds, whereas in 4 patients, they occurred spontaneously without corresponding cortical activity. The movements were transient, with a median duration of 24 hours, and resolved within 72 hours despite persistent burst-suppression patterns. Brain MRI in 3 patients demonstrated diffuse anoxic/hypoxic cortical injury with relative brainstem preservation. All patients died after cardiac arrest, with a median survival of 5 days.

Discussion: We propose the term postanoxic oral automatism (PAOA) to describe a distinct, transient oral motor phenomenon characterized by repetitive, chewing-like tongue movements in comatose patients after cardiac arrest. Unlike previous reports confined to burst-suppression EEG patterns, our findings show that PAOA can occur in both burst-suppression and background-suppression EEG backgrounds. These movements likely result from disinhibition of brainstem central pattern generators responsible for rhythmic orofacial activity and may signify severe cortical dysfunction. Although PAOA is associated with poor prognosis, its independent predictive value remains unclear.

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来源期刊
Neurology. Clinical practice
Neurology. Clinical practice CLINICAL NEUROLOGY-
CiteScore
4.00
自引率
0.00%
发文量
77
期刊介绍: Neurology® Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. The journal publishes original articles in all areas of neurogenetics including rare and common genetic variations, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease genes, and genetic variations with a putative link to diseases. Articles include studies reporting on genetic disease risk, pharmacogenomics, and results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology® Genetics, but studies using model systems for treatment trials, including well-powered studies reporting negative results, are welcome.
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