Department of Pain, Sydney Children's Hospital, Randwick.
School of Clinical Medicine, University of New South Wales, Kensington, NSW.
Clin J Pain. 2024 Mar 1;40(3):137-149. doi: 10.1097/AJP.0000000000001189.
This retrospective, cross-sectional study investigated the nature and extent of burden experienced by caregivers of children and adolescents with chronic pain, and factors associated with increased caregiver burden.
The Pediatric Electronic Persistent Pain Outcomes Collaboration database provided prospectively collected data from 1929 families attending 9 pediatric chronic pain services across Australia and New Zealand. Data included demographic information, responses to child pain and functioning measures, caregiver work impairment, and psychosocial functioning.
Caregivers of children with chronic pain reported work impairment associated with their child's pain (mean: 15% ± SD 25 absenteeism; 38% ± SD 29 productivity lost), significantly worse than published international population norms (large-scale community survey data), most other caregiver samples of adults and children with other chronic conditions, and adult samples with various pain conditions. Caregivers reported considerable burden in multiple psychosocial functioning domains, particularly leisure functioning, pain-related catastrophizing, and adverse parenting behaviors (with greater pain-related avoidance). Caregiver psychosocial burden was significantly associated with child psychosocial functioning (β = -0.308, P < 0.01), school absenteeism (β = 0.161, P < 0.01), physical disability (β = 0.096, P < 0.05), and pain duration (β = 0.084, P < 0.05), but not pain intensity. Caregiver work productivity loss was significantly associated with school absenteeism (β = 0.290, P < 0.01), child physical disability (β = 0.148, P < 0.01), child health care utilization (β = 0.118, P < 0.05), and worst pain intensity (β = 0.101, P < 0.05).
These results highlight the significant and varied impacts experienced by caregivers of children with chronic pain. This work is novel in reporting significant work impairment and confirms psychosocial burden in a larger sample than previous studies.
本回顾性、横断面研究调查了儿童和青少年慢性疼痛患者照顾者所经历的负担的性质和程度,以及与照顾者负担增加相关的因素。
儿科电子持续性疼痛结果合作数据库提供了来自澳大利亚和新西兰 9 个儿科慢性疼痛服务机构的 1929 个家庭的前瞻性收集数据。数据包括人口统计学信息、儿童疼痛和功能测量的反应、照顾者工作障碍以及心理社会功能。
患有慢性疼痛的儿童的照顾者报告与孩子的疼痛相关的工作障碍(平均:15%±25%缺勤;38%±29%生产力损失),明显比国际大规模社区调查数据的普通人群、其他大多数照顾者样本(成人和患有其他慢性疾病的儿童)以及患有各种疼痛疾病的成人样本更差。照顾者在多个心理社会功能领域报告了相当大的负担,特别是休闲功能、与疼痛相关的灾难化、以及不良的育儿行为(与更多的疼痛相关的回避)。照顾者的心理社会负担与儿童的心理社会功能(β=-0.308,P<0.01)、学校缺勤(β=0.161,P<0.01)、身体残疾(β=0.096,P<0.05)和疼痛持续时间(β=0.084,P<0.05)显著相关,但与疼痛强度无关。照顾者的工作生产力损失与学校缺勤(β=0.290,P<0.01)、儿童身体残疾(β=0.148,P<0.01)、儿童医疗保健利用(β=0.118,P<0.05)和最严重的疼痛强度(β=0.101,P<0.05)显著相关。
这些结果突出了儿童慢性疼痛患者照顾者所经历的重大而多样的影响。这项工作的新颖之处在于报告了重大的工作障碍,并在比以前的研究更大的样本中证实了心理社会负担。