Division of Hematology and Oncology, Department of Pediatrics, Washington University School of Medicine, 4523 Clayton Avenue, Campus Box 8005, St. Louis, MO, 63110, USA.
Section of Pediatric Palliative Care, Texas Children's Hospital, Houston, TX, USA.
Support Care Cancer. 2020 Mar;28(3):1215-1222. doi: 10.1007/s00520-019-04933-8. Epub 2019 Jun 20.
Parents of children with cancer make treatment decisions in highly emotional states while feeling overwhelmed with information. In previous work, 1 in 6 parents demonstrated heightened decisional regret regarding treatment at diagnosis. However, it is unclear how regret evolves over time. We aimed to determine whether parents of children with cancer experience decisional regret over time and to identify parental characteristics and clinician behaviors associated with longitudinal regret.
Prospective, questionnaire-based cohort study of parents of children with cancer at two academic pediatric hospitals. Parents reported decisional regret at diagnosis, 4 months, and 12 months.
At baseline, 13% of parents (21/158) reported heightened regret, 11% (17/158) at 4 months (p = 0.43, McNemar's test relative to baseline), and 11% (16/158) at 12 months (p = 0.35 relative to baseline and p = 0.84 relative to 4 months). In multivariable analysis using generalized estimating equations adjusted for the time point of survey completion, heightened regret was associated with non-white race/ethnicity (OR 11.57, 95% CI 3.53 to 41.05, p < .0001) and high anxiety (OR 2.01, 95% CI 1.04 to 3.90, p = .04). Parents with high peace of mind (OR 0.24, 95% CI 0.09 to 0.62, p = .003) and those reporting high-quality information (OR 0.22, 95% CI 0.07 to 0.69, p = 0.01) had lower odds of heightened regret. We found no association between heightened regret and the time point of survey administration.
A small, significant proportion of parents experience heightened regret throughout the first year of their child's cancer treatment; non-white parents are at higher risk. Effective communication may protect against regret.
癌症患儿的父母在做出治疗决策时情绪激动,同时也感到信息过载。在之前的研究中,1/6 的父母在诊断时表现出对治疗的高度后悔。然而,目前尚不清楚这种后悔感是否会随着时间的推移而变化。我们旨在确定癌症患儿的父母是否会随着时间的推移而产生决策后悔感,并确定与纵向后悔相关的父母特征和临床医生行为。
前瞻性、基于问卷的队列研究,研究对象为两家学术儿科医院的癌症患儿的父母。父母在诊断时、4 个月和 12 个月时报告决策后悔感。
在基线时,13%的父母(21/158)报告存在高度后悔感,4 个月时为 11%(17/158)(p=0.43,与基线相比 McNemar 检验),12 个月时为 11%(16/158)(p=0.35 与基线相比,p=0.84 与 4 个月时相比)。使用广义估计方程进行多变量分析,根据调查完成时间点进行调整,高度后悔感与非白种人种族/民族(OR 11.57,95%CI 3.53 至 41.05,p<0.0001)和高焦虑(OR 2.01,95%CI 1.04 至 3.90,p=0.04)相关。心态平和的父母(OR 0.24,95%CI 0.09 至 0.62,p=0.003)和报告高质量信息的父母(OR 0.22,95%CI 0.07 至 0.69,p=0.01)出现高度后悔感的几率较低。我们没有发现高度后悔感与调查管理时间点之间存在关联。
在患儿癌症治疗的第一年,一小部分父母会经历高度后悔感;非白种人父母的风险更高。有效的沟通可能会预防后悔。