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Factors associated with caregiving burden and mental health conditions in caregivers of patients with anorexia nervosa in Japan

机译:日本神经性厌食症患者护理人员的护理负担和心理健康状况的相关因素

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Background There are no studies about the caregiving burdens in families of patients with eating disorders in Japan, and only limited studies on the role of caregivers’ stress coping, social support, and mental health. This study examines caregiving burdens, mental health conditions, and associated factors in caregivers of anorexia nervosa (AN) patients in Japan. Methods Seventy-nine principal caregivers (70 mothers, 5 fathers, 3 spouses and 1 grandmother; mean age 56.0?±?8.0?years) for outpatients with AN (all female; mean age 26.6?±?7.9?years; BMI 14.6?±?3.2?kg/m2) were evaluated using self-report questionnaires in a cross-sectional study. The questionnaires included caregiving burden (J-ZBI_8), mental health conditions (GHQ28), stress coping styles (CISS), social support (SNQ), severity of the patient’s symptoms from the family’s perspective (ABOS), and family functioning (GF-FAD). Clinical information about the patients was also obtained. Results Mean caregiving burden assessed by J-ZBI_8 score was 12.4?±?7.0 (SD). The total GHQ score was 31.6?±?13.7 (Likert scoring) and 9.2?±?7.0 (GHQ scoring). Of the respondents, 48 (60.7?%) indicated a high risk for mental health problems that exceeded the cutoff point of the GHQ. Significantly higher caregiving burden and poor mental health conditions were shown in the group who had contact with patients?>?6?h a day compared to the group with daily patient contact?2?=?0.401), while predictors of mental health conditions were Emotion-Oriented Coping ( β =?0.522, p 2?=?0.602). Conclusion Caregivers of AN patients experienced heavy burdens and manifested poor mental health conditions. The severity of the patient’s symptoms from the family’s perspective and the greater use of emotion-oriented coping were associated with higher burdens. Greater use of emotion-oriented coping, less affective support and longer contact with patients were related to worse mental health conditions. Interventions to promote caregivers’ adaptive coping styles may help reduce their caregiving burden and improve their mental health.
机译:背景技术在日本,没有关于饮食失调患者家庭的照料负担的研究,而关于照料者的压力应对,社会支持和心理健康的作用的研究还很有限。这项研究调查了日本神经性厌食症(AN)患者的照料者的照料负担,心理健康状况和相关因素。方法:对门诊AN患者(全部为女性;平均年龄26.6±7.9岁; BMI 14.6岁)的七十九名主要护理人员(母亲70名,父亲5名,配偶3名,祖母1名;平均年龄56.0±8.0岁)。在一项横断面研究中,使用自我报告调查表对±?3.2?kg / m 2 )进行了评估。问卷包括护理负担(J-ZBI_8),精神健康状况(GHQ28),压力应对方式(CISS),社会支持(SNQ),从家庭角度看患者症状的严重程度(ABOS)和家庭功能(GF- FAD)。还获得了有关患者的临床信息。结果J-ZBI_8评分评估的平均护理负担为12.4±±7.0(SD)。总体GHQ得分为31.6±±13.7(利克特评分)和9.2±±7.0(GHQ评分)。在受访者中,有48名(60.7%)表示精神健康问题的风险很高,超过了GHQ的临界点。与每天接触患者的组相比,每天接触患者> 6?ha的组显示出更高的照料负担和较差的心理健康状况[2 ?=?0.401),而精神疾病的预测因子健康状况为情绪应对(β=?0.522,p 2 ?=?0.602)。结论AN患者的护理人员负担沉重,心理健康状况较差。从家庭的角度来看,患者症状的严重程度以及更多地使用情感导向的应对方式会带来更高的负担。大量使用情绪导向的应对方法,较少的情感支持以及与患者的长时间接触与更差的心理健康状况有关。采取干预措施来提高护理人员的适应性应对方式可能有助于减轻其护理负担并改善其心理健康。

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