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治愈希望渺茫的儿童:父母对孩子健康相关生活质量的代理及其在治疗期间对父母身心健康的影响。

Children with minimal chance for cure: parent proxy of the child's health-related quality of life and the effect on parental physical and mental health during treatment.

作者信息

Mandrell Belinda N, Baker Justin, Levine Deena, Gattuso Jami, West Nancy, Sykes April, Gajjar Amar, Broniscer Alberto

机构信息

Department of Pediatric Medicine, Division of Nursing Research, St. Jude Children's Research Hospital, 262 Danny Thomas Place, MS 728, Memphis, TN, 38105-2794, USA.

Department of Oncology, Division of Quality of Life and Palliative Care, Palliative Care, St. Jude Children's Research Hospital, Memphis, TN, USA.

出版信息

J Neurooncol. 2016 Sep;129(2):373-81. doi: 10.1007/s11060-016-2187-9. Epub 2016 Jun 25.

Abstract

To assess health-related quality of life (HRQOL) from the time of diagnosis until disease progression in a cohort of children with diffuse intrinsic pontine glioma (DIPG). The assessment was collected from the perspectives of the child and their parents and evaluated the effect of the child's HRQOL on their parents' physical and mental well-being, thus providing insight into the optimal timing of palliative consultation, including anticipatory grief and bereavement services. This longitudinal study assessed 25 parents and their children, ages 2-17 years of age with DIPG across five time-points, baseline and weeks 2, 4, 6, 16, 24. Assessments included the PedsQL 4.0 Core Scales, PedsQL 3.0 Brain Tumor Scale, and Short-Form 36. HRQOL instruments were completed by the child (age ≥5 years) and parent-proxy (ages 2-17 years), with the parent completing the SF-36. Children's reports and parents' proxy of their child's HRQOL indicated poor physical functioning and increased anxiety at the initiation of therapy. A trending improvement in the children's HRQOL was reported by children and parents from baseline to week 6, with a decline at week 16. The childs' parent proxy reported cognitive problems, procedural anxiety and lower overall brain tumor HRQOL were assoicated with poorer self-reported parental mental status. Palliative care consultation should be initiated at the time of diagnosis and is supported in the high physical and emotional symptom burden reported by our patients, with heightened involvement initiated at 16 weeks. Prompt palliative care involvement, mitigating anxiety associated with clinic visits and procedures, management of brain tumor specific symptoms, advanced care planning, anticipatory grief and bereavement services, and care coordination may maximize HRQOL for patients and ensure positive long-term outcomes for parents of children with DIPG.

摘要

评估弥漫性脑桥内在胶质瘤(DIPG)患儿队列从诊断时到疾病进展期间的健康相关生活质量(HRQOL)。评估从患儿及其父母的角度收集,并评估患儿的HRQOL对其父母身心健康的影响,从而深入了解姑息治疗咨询的最佳时机,包括预期性悲伤和丧亲服务。这项纵向研究在五个时间点评估了25名父母及其2至17岁患有DIPG的孩子,时间点分别为基线以及第2、4、6、16、24周。评估包括儿童生活质量量表4.0核心量表、儿童生活质量量表3.0脑肿瘤量表和简明健康调查问卷36项。HRQOL工具由儿童(年龄≥5岁)和家长代理(年龄2至17岁)完成,家长完成简明健康调查问卷36项。儿童报告及其父母对其HRQOL的代理报告表明,治疗开始时身体功能较差且焦虑增加。儿童和父母报告,从基线到第6周儿童的HRQOL有上升趋势,在第16周下降。儿童的家长代理报告称认知问题、程序性焦虑和较低的总体脑肿瘤HRQOL与家长自我报告的较差心理状态相关。应在诊断时开始姑息治疗咨询,这得到了我们患者报告的高身体和情感症状负担的支持,在第16周开始加强参与。及时的姑息治疗参与、减轻与门诊就诊和治疗程序相关的焦虑、管理脑肿瘤特定症状、进行高级护理规划、提供预期性悲伤和丧亲服务以及护理协调,可能会使患者的HRQOL最大化,并确保DIPG患儿父母获得积极的长期结果。

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