Faculty of Health Sciences and Medicine, University of Lucerne, Lucerne, Switzerland.
Oslo Centre for Biostatistics and Epidemiology, Oslo University Hospital, Oslo, Norway.
Pediatr Blood Cancer. 2024 Aug;71(8):e31095. doi: 10.1002/pbc.31095. Epub 2024 Jun 2.
Childhood cancer survivors may experience psychological distress due to the disease, cancer treatments, and potential late effects. Limited knowledge exists regarding longitudinal changes in psychological distress after childhood cancer. We aimed to determine changes in psychological distress over time and explore determinants of changes.
The Swiss Childhood Cancer Survivor Study collected data at baseline (2007-2009) and follow-up (2010-2012). Psychological distress was measured using the Brief Symptom Inventory 18 (BSI-18), including three symptom scales (somatization, depression, anxiety) and an overall distress index (Global Severity Index, GSI). Sum-scores were T-standardized (mean = 50; standard deviation [SD] = 10). Survivors with a score ≥57 on the GSI or two symptom scales were classified as cases with distress. We used linear mixed effects regression to identify potential sociodemographic and clinical determinants of change in psychological distress.
We analyzed 696 survivors at baseline (mean age = 24 years [SD = 4], 49% females, mean time since diagnosis = 16 years [SD = 4]). On follow-up (2.4 years, SD = 1), 317 survivors were analyzed, including 302 participants with repeated measures. We found that 13% (39/302) were cases at baseline, and 25% (76/302) were cases on follow-up. Those older at study and longer since diagnosis, females, diagnosed with central nervous system (CNS) tumors, and those reporting late effects were more likely to experience higher levels of distress. Females and unemployed are at higher risk for developing or persisting psychological distress than males and those who are employed or in training.
We observed an increase in psychological distress score over time, with higher proportion of psychological distress on follow-up. Anticipatory guidance and screening should be implemented in regular follow-up care.
儿童癌症幸存者可能会因疾病、癌症治疗和潜在的晚期影响而经历心理困扰。关于儿童癌症后心理困扰的纵向变化,知识有限。我们旨在确定随时间的变化和探索变化的决定因素。
瑞士儿童癌症幸存者研究在基线(2007-2009 年)和随访(2010-2012 年)时收集数据。使用Brief Symptom Inventory 18(BSI-18)测量心理困扰,包括三个症状量表(躯体化、抑郁、焦虑)和一个总体困扰指数(Global Severity Index,GSI)。总分进行 T 标准化(均值=50;标准差[SD]=10)。GSI 或两个症状量表得分≥57 的幸存者被归类为有困扰的病例。我们使用线性混合效应回归来确定心理困扰变化的潜在社会人口统计学和临床决定因素。
我们分析了基线时的 696 名幸存者(平均年龄 24 岁[SD=4],49%为女性,平均诊断后时间 16 年[SD=4])。在随访(2.4 年,SD=1)时,分析了 302 名幸存者中的 317 名,其中包括 302 名重复测量的参与者。我们发现,13%(39/302)在基线时为病例,25%(76/302)在随访时为病例。研究时年龄较大、诊断后时间较长、女性、诊断为中枢神经系统(CNS)肿瘤以及报告晚期影响的幸存者更有可能经历更高水平的困扰。女性和失业者比男性和就业或接受培训者更有可能出现或持续存在心理困扰。
我们观察到心理困扰评分随时间的增加而增加,随访时的心理困扰比例更高。应在定期随访护理中实施预期指导和筛查。