The relationship between psychosocial risk and neurocognitive functioning early after childhood central nervous system tumour diagnosis.

IF 1.8 4区 心理学 Q2 PSYCHOLOGY
Jessica Beamish, Riley M Damiano, Josephine Drijver, Femke Aarsen, Martha Grootenhuis, Marita Partanen
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Abstract

Neurocognitive impairments are common in paediatric central nervous system (CNS) tumours and can relate to clinical and demographic factors. The impact of social or environmental factors, such as family psychosocial risk, is less well understood. We examined neurocognitive functioning in children with CNS tumours shortly after diagnosis and associations with psychosocial risk. This cohort study included children who underwent neuropsychological assessments within three months of diagnosis. Proportion, chi-square and t-tests were used to compare neurocognitive outcomes to norms and evaluate prevalence of neurocognitive impairment (International Cognition and Cancer Task Force criteria: two scores at z ≤ -1.5, one score at z ≤ -2 or both). Regression analyses examined associations between psychosocial risk, age at diagnosis and neurocognitive outcomes, controlling for medical factors. We included 125 children (47 females; mean age at diagnosis = 9.7 years) assessed at an average of 2.08 months after diagnosis. A larger proportion of patients demonstrated neurocognitive impairments than normative expectations (p = .002), with a greater likelihood for children from increased psychosocial risk groups (p = .014). Increased psychosocial risk was associated with lower parent-reported executive functioning (p = .028), but not with other neurocognitive outcomes. Midline tumour location was related to better working memory; history of obstructive hydrocephalus was related to poorer verbal memory and chemo/radiotherapy initiation was related to poorer processing speed (p's < .05). A sub-group of children with CNS tumours show neurocognitive impairments shortly after diagnosis. Children with increased family psychosocial risk were at higher risk of impairment. Psychosocial risk can help identify neurocognitively vulnerable children, highlighting the importance of both neuropsychological and psychosocial screening.

儿童中枢神经系统肿瘤诊断后早期心理社会风险与神经认知功能的关系。
神经认知障碍在小儿中枢神经系统(CNS)肿瘤中很常见,可能与临床和人口因素有关。社会或环境因素(如家庭心理风险)的影响尚不清楚。我们检查了诊断后不久患有中枢神经系统肿瘤的儿童的神经认知功能及其与社会心理风险的关系。这项队列研究包括在诊断三个月内接受神经心理学评估的儿童。采用比例检验、卡方检验和t检验比较神经认知结果与标准,并评估神经认知障碍的患病率(国际认知和癌症工作组标准:两个分数在z≤-1.5,一个分数在z≤-2或两者兼有)。回归分析检查了心理社会风险、诊断年龄和神经认知结果之间的关联,控制了医学因素。我们纳入125名儿童(47名女性,诊断时平均年龄为9.7岁),在诊断后平均2.08个月进行评估。表现出神经认知障碍的患者比例高于规范预期(p =。002),来自高社会心理风险群体的儿童更有可能(p = .014)。增加的心理社会风险与较低的父母报告的执行功能相关(p =。028),但与其他神经认知结果无关。中线肿瘤位置与较好的工作记忆有关;梗阻性脑积水病史与较差的言语记忆有关,化疗/放疗起始与较差的处理速度有关
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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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