The vanishing of the ACoA syndrome after aneurysmal subarachnoid haemorrhage: New era, different management, fewer problems?

IF 2 4区 心理学 Q2 PSYCHOLOGY
A. M. Buunk, J. M. Spikman, M. Wagemakers, J. R. Jeltema, J. de Vries, A. Mazuri, M. Uyttenboogaart, R. J. M. Groen
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Abstract

Historically, a specific set of symptoms has been related to the rupture and repair of anterior communicating artery (ACoA) aneurysms. These consequences were defined as the ‘ACoA syndrome’ and included observations of severe memory loss, confabulation and personality or behavioural changes. These observations correspond to neuropsychological impairments in memory, executive functions and social cognition. However, in more recent studies, the existence of such a distinct syndrome has been called into question. We aimed to investigate the existence of the ACoA syndrome, by combining analysis of our own data with a systematic review of the literature. Memory, executive functions and social cognition of subarachnoid haemorrhage patients with ACoA aneurysms (N = 28) were compared to patients with aneurysms in other locations (N = 66). Results showed no significant differences. Subsequently, a systematic review of the existing literature on the ACoA syndrome was performed using Embase and PubMed until October 2022. Studies that investigated cognitive functions after rupture and repair of ACoA aneurysms were included. The search yielded 847 unique entries and after screening titles and abstracts, 648 records were excluded. 199 full-text articles were assessed for eligibility and 55 articles were included. Evidence was found for the ACoA syndrome in studies between 1960 and 2000, with impairments in memory and executive problems in the majority of studies. However, the majority of studies from 2000 did not demonstrate a distinct ACoA syndrome, although neuropsychological measurements improved. This coincides with the changes in the management of ACoA aneurysms over the past decades, such as the emergence of endovascular treatment and improvement of neurointensive care. Therefore, we hypothesize that the management techniques of ACoA aneurysms until around 2000, i.e. mainly conventional clipping, could be related to the presence of symptoms of the ACoA syndrome.

Abstract Image

动脉瘤性蛛网膜下腔出血后ACoA综合征的消失:新时代,不同的管理,更少的问题?
历史上,一组特定的症状与前交通动脉瘤的破裂和修复有关。这些后果被定义为“ACoA综合征”,包括严重记忆力丧失、会话和个性或行为变化。这些观察结果与记忆、执行功能和社会认知方面的神经心理障碍相对应。然而,在最近的研究中,这种独特综合征的存在受到了质疑。我们的目的是通过将我们自己的数据分析与文献的系统综述相结合来调查ACoA综合征的存在。蛛网膜下腔出血伴ACoA动脉瘤患者的记忆、执行功能和社会认知(N = 28)与其他位置的动脉瘤患者进行比较(N = 66)。结果显示没有显著差异。随后,使用Embase和PubMed对ACoA综合征的现有文献进行了系统综述,直到2022年10月。研究包括ACoA动脉瘤破裂和修复后的认知功能。搜索得到847个独特的条目,在筛选标题和摘要后,648条记录被排除在外。对199篇全文文章的合格性进行了评估,纳入了55篇文章。在1960年至2000年的研究中发现了ACoA综合征的证据,在大多数研究中都有记忆障碍和执行问题。然而,2000年的大多数研究并没有显示出明显的ACoA综合征,尽管神经心理学测量有所改善。这与过去几十年来ACoA动脉瘤管理的变化相吻合,例如血管内治疗的出现和神经重症监护的改善。因此,我们假设,直到2000年左右,ACoA动脉瘤的治疗技术,即主要是传统的夹闭术,可能与ACoA综合征症状的存在有关。
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来源期刊
Journal of Neuropsychology
Journal of Neuropsychology 医学-心理学
CiteScore
4.50
自引率
4.50%
发文量
34
审稿时长
>12 weeks
期刊介绍: The Journal of Neuropsychology publishes original contributions to scientific knowledge in neuropsychology including: • clinical and research studies with neurological, psychiatric and psychological patient populations in all age groups • behavioural or pharmacological treatment regimes • cognitive experimentation and neuroimaging • multidisciplinary approach embracing areas such as developmental psychology, neurology, psychiatry, physiology, endocrinology, pharmacology and imaging science The following types of paper are invited: • papers reporting original empirical investigations • theoretical papers; provided that these are sufficiently related to empirical data • review articles, which need not be exhaustive, but which should give an interpretation of the state of research in a given field and, where appropriate, identify its clinical implications • brief reports and comments • case reports • fast-track papers (included in the issue following acceptation) reaction and rebuttals (short reactions to publications in JNP followed by an invited rebuttal of the original authors) • special issues.
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