Ecole de Réadaptation, Faculté de Médecine, Université de Montréal, the Montreal Children's Hospital, Groupe de Recherche Interdisciplinaire en Santé and the Public Health Department, Montreal, Quebec, Canada.
Pediatr Rheumatol Online J. 2009 Mar 11;7:7. doi: 10.1186/1546-0096-7-7.
Parents of children with a chronic condition such as juvenile arthritis must cope with greater demands than those living with a healthy child. They must adopt different behaviours in order to lessen the impact on the family structure. Parental coping refers to the parent's specific cognitive and behavioural efforts to reduce or manage a demand on the family system. The aims of this study were: to describe coping in a cohort of parents of children with JIA; to determine whether quality of life is associated with parental coping; to explore whether socio-demographic factors such as child's age, family socioeconomic status and family structure are associated with parental coping. One hundred eighty-two parents caring for a child with JIA completed a postal survey at three times over a one-year period, which included the Juvenile Arthritis Quality of Life Questionnaire (JAQQ), the Coping Health Inventory for Parents (CHIP) and questionnaires describing socio-demographic characteristics. Linear mixed models were employed to analyse the association between the child's quality of life and parental coping. Mean total QoL scores (JAQQ) showed that children experienced difficulty in completing specified activities at most just below 25% of the time and results fall off slightly following the 6 month time point. Mean parental coping scores for the CHIP subscales at baseline were 38.4 +/- 9.0, 33.4 +/- 11.6, 16.5 +/- 6.1, for Maintaining Family Integration (maximum score 57), Maintaining Social Support (maximum score 54) and Understanding the Medical Situation (maximum score 24), respectively. Understanding the Medical Situation was deemed most useful. The child's QoL was associated with parental coping. Parents of children with greater psychosocial dysfunction used more coping behaviours related to Understanding the Medical Situation (beta coefficient, 0.73; 95% CI, 0.01, 1.45). These findings underscore the importance of helping parents of children with JIA better understand their child's medical situation.
父母照顾患有慢性疾病(如幼年特发性关节炎)的孩子,其需求比照顾健康孩子的父母更大。他们必须采取不同的行为方式,以减轻对家庭结构的影响。父母应对是指父母为减轻或管理家庭系统的需求而采取的特定认知和行为努力。本研究的目的是:描述幼年特发性关节炎患儿父母的应对方式;确定生活质量是否与父母应对方式相关;探讨儿童年龄、家庭社会经济地位和家庭结构等社会人口因素是否与父母应对方式相关。182 名照顾幼年特发性关节炎患儿的父母在一年的三个时间点完成了一项邮寄调查,调查内容包括幼年特发性关节炎生活质量问卷(JAQQ)、父母应对健康问卷(CHIP)和描述社会人口特征的问卷。采用线性混合模型分析儿童生活质量与父母应对方式之间的关系。JAQQ 的平均总生活质量评分(QoL)显示,儿童在大多数指定活动中完成困难,最接近 25%的时间,结果在 6 个月后略有下降。基线时 CHIP 子量表的平均父母应对评分分别为 38.4+/-9.0、33.4+/-11.6、16.5+/-6.1,用于维持家庭融合(最高得分为 57)、维持社会支持(最高得分为 54)和理解医疗情况(最高得分为 24)。理解医疗情况被认为最有用。儿童的生活质量与父母的应对方式有关。心理社会功能障碍较大的儿童的父母使用了更多与理解医疗情况相关的应对行为(β系数,0.73;95%置信区间,0.01,1.45)。这些发现强调了帮助幼年特发性关节炎患儿的父母更好地了解其子女医疗情况的重要性。