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胶质母细胞瘤长期幸存者的神经认知和社会人口统计学功能。

Neurocognitive and sociodemographic functioning of glioblastoma long-term survivors.

机构信息

Department of Medicine I, Medical University of Vienna, Austria Comprehensive Cancer Center - Central Nervous System Tumours Unit (CCC-CNS), Währinger Gürtel 18-20, 1090, Vienna, Austria.

出版信息

J Neurooncol. 2012 Sep;109(2):331-9. doi: 10.1007/s11060-012-0897-1. Epub 2012 May 29.

DOI:10.1007/s11060-012-0897-1
PMID:22644537
Abstract

An increasing number of patients with glioblastoma multiforme live longer than 3 years after diagnosis (long-term survivors). Even so, little is known about their everyday performance and quality of life. We studied 17 glioblastoma patients surviving for longer than 3 years. We assessed all patients using the computerized neurocognitive assessment instrument NeuroCog FX test, the EORTC QLQ-C30, the EORTC QLQ-BN20, the Hospital Anxiety and Depression Scale, the Ten-Meter Walking Test, the Nine Hole Peg Test, the Boston Aphasia Severity Scale, and the Activities of Daily Living and Instrumental Activities of Daily Living forms. We included 9 female and 8 male glioblastoma long-term survivors with a median age of 51 years (24-71). The majority of the patients (10/17) scored normal in the NeuroCog FX test. However, financial difficulties, reduced social and cognitive functioning, and future uncertainty were frequently reported. Three patients showed conspicuous depression scores, two had noticeable anxiety results. Drowsiness and fatigue were the most often reported physical complaints. There were 12/17 patients who were fully independent concerning activities of daily living and 14 patients (82%) showed ≥90 points in the Barthel Index, but 6 patients (35%) were impaired in their manual dexterity, and 1 patient in mobility. Glioblastoma long-term survivors show moderate impairment in their cognitive functions and more often neurological symptoms. However, the majority of these patients are able to manage their daily routine independently. Nevertheless, future prospects remain poor and patients suffer from financial difficulties.

摘要

越来越多的多形性胶质母细胞瘤患者在诊断后能存活 3 年以上(长期幸存者)。即便如此,人们对他们的日常表现和生活质量知之甚少。我们研究了 17 名生存时间超过 3 年的胶质母细胞瘤患者。我们使用计算机化神经认知评估工具 NeuroCog FX 测试、EORTC QLQ-C30、EORTC QLQ-BN20、医院焦虑抑郁量表、10 米步行测试、九孔钉测试、波士顿失语症严重程度量表以及日常生活活动和工具性日常生活活动形式对所有患者进行评估。我们纳入了 9 名女性和 8 名男性胶质母细胞瘤长期幸存者,中位年龄为 51 岁(24-71 岁)。大多数患者(17 例中的 10 例)在 NeuroCog FX 测试中得分正常。然而,经济困难、社交和认知功能下降以及未来的不确定性经常被报告。3 名患者出现明显的抑郁评分,2 名患者有明显的焦虑结果。嗜睡和疲劳是最常报告的身体不适。有 12/17 名患者在日常生活活动方面完全独立,14 名患者(82%)在巴氏量表中得分≥90 分,但 6 名患者(35%)在手部灵巧性方面受损,1 名患者在行动方面受损。胶质母细胞瘤长期幸存者的认知功能有中度受损,且更常出现神经症状。然而,这些患者中的大多数能够独立管理自己的日常生活。尽管如此,未来前景仍然不佳,患者还面临经济困难。

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