[Parental Distress of Patients Who Refuse to Eat: Toward a Deeper Understanding and Greater Support for Parents of Children Suffering from an Eating Disorder].

IF 1 4区 医学 Q4 PSYCHIATRY
Beate Herpertz-Dahlmann, Ingar Zielinski-Gussen
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引用次数: 0

Abstract

Parental Distress of Patients Who Refuse to Eat: Toward a Deeper Understanding and Greater Support for Parents of Children Suffering from an Eating Disorder Abstract: Many parents experience their role as parents of a daughter/son with anorexia nervosa as very troublesome and demanding. In several departments of child and adolescen psychiatry in Germany, the contact between parents and adolescent patients with anorexia nervosa is still restricted because parents are often judged responsible for the eating disorder of their child - or at least seen as troublemakers during their child's inpatient treatment. Parents blame themselves for the development of anorexia nervosa, and in comparison to other mental disorders of adolescence, they experience even more guilt and shame. Many of them suffer from psychiatric disorders themselves (not a few from eating disorders), which reinforce feelings of helplessness and shame. Several parents have partnership problems and must take off work to support their child, which often leads to financial losses for the whole family. They complain that they have insufficient support and feel misunderstood by health professionals whom they wish to have a profound knowledge of the disorder and who would trust and understand the carers. This article provides several recommendations to improve the relationship between parents and therapists: termination of contact restrictions, detailed information for the parents about possible biological and psychological causes of eating disorders, including psychoeducational groups and involvement in treatment, not only through therapeutic conversations but also through practical exercises such as meal support. An innovative approach is home treatment, which offers the chance to integrate parents into treatment and thus improve their skills in handling their daughter´s/son´s illness. We should be aware that parents are the most important resource to help young patients with debilitating eating disorders.

[拒绝进食患者的父母痛苦:对患有饮食失调儿童的父母的更深理解和更大支持]。
摘要:许多父母都认为,作为患有神经性厌食症的女儿/儿子的父母,他们的角色是非常麻烦和苛刻的。在德国的几个儿童和青少年精神病学部门,父母和患有神经性厌食症的青少年患者之间的接触仍然受到限制,因为父母经常被认为对孩子的饮食失调负有责任——或者至少在孩子住院治疗期间被视为麻烦制造者。父母将神经性厌食症的发展归咎于自己,与青少年的其他精神障碍相比,他们感到更多的内疚和羞耻。他们中的许多人本身患有精神疾病(不少人患有饮食失调),这加剧了他们的无助感和羞耻感。一些父母的伴侣关系出现问题,不得不辞掉工作来抚养孩子,这往往会给整个家庭带来经济损失。他们抱怨说,他们没有得到足够的支持,并感到被卫生专业人员误解,他们希望这些专业人员对这种疾病有深刻的了解,并信任和理解护理人员。本文提供了一些改善父母和治疗师之间关系的建议:终止接触限制,为父母提供有关饮食失调可能的生理和心理原因的详细信息,包括心理教育小组和参与治疗,不仅通过治疗性对话,还通过实际练习,如膳食支持。一种创新的方法是家庭治疗,它使父母有机会参与治疗,从而提高他们处理女儿/儿子疾病的技能。我们应该意识到,父母是帮助患有饮食失调症的年轻患者最重要的资源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.90
自引率
16.70%
发文量
74
期刊介绍: Die Zeitschrift veröffentlicht Originalarbeiten, Übersichtsreferate, Fallberichte, aktuelle Mitteilungen und Buchbesprechungen und informiert laufend über die Arbeit anderer internationaler Fachzeitschriften. Sie ist offizielles Organ der Deutschen Gesellschaft für Kinder- und Jugendpsychiatrie, Psychosomatik und Psychotherapie.
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