Neuropsychological Changes After Surgery for Anterior Communicating Artery Aneurysm

Neuropsychological disturbances following surgery for anterior communicating artery aneurysms were analyzed in 26 patients (11 males, 15 females) using the Hasegawa dementia scale-revised (HDS-R) over a 3-year period. The patients were aged from 34 to 76 years (mean 54.1 years). Lesions in the front...

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Published inNeurologia medico-chirurgica Vol. 40; no. 2; pp. 83 - 87
Main Authors JIMBO, Hiroyuki, HANAKAWA, Kazuo, OZAWA, Hiroshi, DOHI, Kenji, SAWABE, Yoshiharu, MATSUMOTO, Kiyoshi, NAGATA, Kazuya
Format Journal Article
LanguageEnglish
Japanese
Published Japan The Japan Neurosurgical Society 2000
THE JAPAN NEUROSURGICAL SOCIETY
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Summary:Neuropsychological disturbances following surgery for anterior communicating artery aneurysms were analyzed in 26 patients (11 males, 15 females) using the Hasegawa dementia scale-revised (HDS-R) over a 3-year period. The patients were aged from 34 to 76 years (mean 54.1 years). Lesions in the frontal lobe were evaluated using computed tomography (CT). Twenty-three patients had symptoms over the course. Four patients had basal forebrain lesion, five had ventral frontal lesion, and 12 had no lesion. Patients with basal forebrain lesion and no lesion tended to show disorientation. The mean HDS-R score was 10.2 points in the patients with ventral frontal lesion, and 13.5 points in the patients with no lesion. These scores are within the range for dementia. The mean HDS-R score in patients with basal forebrain and striate lesions was over 25 points and beyond the range for dementia. Significant differences were observed in the HDS-R score between patients with ventral frontal lesion and basal forebrain lesion, and between patients with no lesion and basal forebrain lesion (p < 0.05). Recovery from neuropsychological disturbances was poorer in patients with ventral frontal lesion and no lesion compared to those with basal forebrain and striate lesions, and their symptoms tended to persist.
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ISSN:0470-8105
1349-8029
DOI:10.2176/nmc.40.83