Parker Clare, Schilstra Clarissa E, McCleary Karen, Martin Michelle, Trahair Toby N, Kotecha Rishi S, Ramachandran Shanti, Cockcroft Ruellyn, Conyers Rachel, Cross Siobhan, Dalla-Pozza Luciano, Downie Peter, Revesz Tamas, Osborn Michael, Marshall Glenn M, Wakefield Claire E, Mateos Marion K, Fardell Joanna E
Children's Cancer Centre, Monash Children's Hospital, Clayton, VIC 3168, Australia.
Behavioural Sciences Unit, Kids Cancer Centre, Sydney Children's Hospital, Randwick, NSW 2031, Australia.
Cancers (Basel). 2025 Apr 6;17(7):1238. doi: 10.3390/cancers17071238.
Parents of children with acute lymphoblastic leukaemia (ALL) experience emotional distress throughout their child's treatment course. This study describes the psychological experience of Australian and New Zealand parents of children diagnosed with ALL. This prospective, longitudinal study assessed distress, anxiety, depression, anger and the need for help in parents of children with newly diagnosed ALL across eight sites between October 2018 and November 2022. Psychological symptoms were quantified using the Emotion Thermometer (ET) tool and Patient-Reported Outcome Measurement Information System (PROMIS) questionnaires. Participants were recruited within ninety days of chemotherapy commencement, with surveys distributed bimonthly thereafter. One hundred and seventeen participants completed 327 survey responses spanning 0 to 62 months post-diagnosis. Parental distress peaked within the first 6 months and 40% of parents reported clinically significant symptoms across four or more domains as measured by our questionnaires. Anxiety was the most consistently elevated symptom, with over 50% of responses above the clinical cut-off. Depression and the need for help also peaked closer to diagnosis and declined over time. In contrast, anger remained stable, with 27% reporting clinically significant scores across all time points. Increased time since diagnosis was significantly associated with reductions in distress, anxiety and depression scores. Australian and New Zealand parents experience high levels of psychological distress within the first six months following their child's diagnosis of ALL. A notable minority continue to report elevated distress levels over time, identifying a need for improved psychological support for family wellbeing throughout the ALL treatment trajectory.
急性淋巴细胞白血病(ALL)患儿的父母在孩子整个治疗过程中都会经历情绪困扰。本研究描述了澳大利亚和新西兰被诊断患有ALL的患儿父母的心理体验。这项前瞻性纵向研究评估了2018年10月至2022年11月期间八个地点新诊断为ALL的患儿父母的困扰、焦虑、抑郁、愤怒以及对帮助的需求。使用情绪温度计(ET)工具和患者报告结局测量信息系统(PROMIS)问卷对心理症状进行量化。参与者在化疗开始后的90天内招募,此后每两个月进行一次调查。117名参与者完成了327份调查回复,涵盖诊断后0至62个月。父母的困扰在头6个月达到峰值,40%的父母在我们的问卷测量中报告了四个或更多领域具有临床意义的症状。焦虑是最持续升高的症状,超过50%的回复高于临床临界值。抑郁和对帮助的需求也在接近诊断时达到峰值,并随时间下降。相比之下,愤怒情绪保持稳定,27%的人在所有时间点都报告了具有临床意义的分数。自诊断以来时间的增加与困扰、焦虑和抑郁评分的降低显著相关。澳大利亚和新西兰的父母在孩子被诊断患有ALL后的头六个月内经历了高水平的心理困扰。相当一部分人随着时间的推移继续报告困扰水平升高,这表明在ALL治疗过程中需要改善对家庭幸福的心理支持。