德国神经病学学会(Deutsche Gesellschaft fr Neurologie)指南“短暂性全局健忘症(TGA)”:s1指南。

Dirk Sander, Thorsten Bartsch, Florian Connolly, Christian Enzinger, Urs Fischer, Nils Nellessen, Holger Poppert, Kristina Szabo, Helge Topka
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引用次数: 2

摘要

简介:2022年,DGN(德国神经学会)发布了一份更新的瞬态全球失忆(TGA)指南。TGA的特征是突然出现逆行性和顺行性健忘症,持续时间为1至24小时(平均6至8小时)。发病率估计为每年每100000人中有3至8人。TGA是一种主要发生在50至70岁之间的疾病。建议:TGA的诊断应在临床上进行。如果出现非典型临床表现或怀疑可能的鉴别诊断,应立即进行进一步诊断。在一定比例的患者中,在海马体(尤其是CA1区)检测到典型的单侧或双侧点状DWI/T2病变,证明了TGA。当在发病后24至72小时之间进行MRI检查时,MRI的灵敏度被认为更高。如果海马外出现额外的DWI变化,应考虑血管病因,并及时进行超声和心脏诊断。脑电图可能有助于区分TGA和罕见的遗忘性癫痫发作,尤其是在复发性遗忘性发作中。患者TGA 结论:没有证据表明TGA在脑缺血、慢性记忆障碍或痴呆相关综合征发作方面存在慢性后遗症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Guideline "Transient Global Amnesia (TGA)" of the German Society of Neurology (Deutsche Gesellschaft für Neurologie): S1-guideline.

Introduction: In 2022 the DGN (Deutsche Gesellschaft für Neurologie) published an updated Transient Global Amnesia (TGA) guideline. TGA is characterized by a sudden onset of retrograde and anterograde amnesia for a period of one to a maximum of 24 h (with an average of 6 to 8 h). The incidence is estimated between 3 and 8 per 100,000 population/year. TGA is a disorder that occurs predominantly between 50 and 70 years.

Recommendations: The diagnosis of TGA should be made clinically. In case of an atypical clinical presentation or suspicion of a possible differential diagnosis, further diagnostics should be performed immediately. The detection of typical unilateral or bilateral punctate DWI/T2 lesions in the hippocampus (especially the CA1 region) in a proportion of patients proves TGA. The sensitivity of MRI is considered higher when performed between 24 and 72 h after onset. If additional DWI changes occur outside the hippocampus, a vascular etiology should be considered, and prompt sonographic and cardiac diagnostics should be performed EEG may help to differentiate TGA from rare amnestic epileptic attacks, especially in recurrent amnestic attacks. TGA in patients < 50 years of age is a rarity, therefore it is mandatory to rapidly search for other causes in particular in younger patients. The cause of TGA is still unknown. Numerous findings in recent years point to a multifactorial genesis. Because the pathomechanism of TGA is not yet clearly known, no evidence-based therapeutic or prophylactic recommendations can be made.

Conclusions: There is no evidence for chronic sequelae of TGA with respect to cerebral ischemia, chronic memory impairment, or the onset of dementia-related syndromes.

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