Faculty of Health and Social Development, School of Nursing, University of British Columbia, British Columbia, Canada.
Faculty of Medicine, Department of Pediatrics, University of British Columbia, British Columbia, Canada.
Ann Allergy Asthma Immunol. 2020 Dec;125(6):674-679. doi: 10.1016/j.anai.2020.05.014. Epub 2020 May 23.
Parents experience a wide range of emotions, specifically stress and anxiety, when their child receives a diagnosis of a food allergy. Managing this health condition and coping with emotions require professional and peer support. Currently, there is a lack of resources and a lack of awareness of the resources that are required to help assist parents in managing their child's food allergy.
To describe parental experiences when caring for a child with food allergy and to review the resources parents need to manage living with a child with food allergy and more specifically how they would want these resources delivered.
A total of 7 semistructured focus groups were conducted in British Columbia, Canada. Parents were asked to describe their experiences with managing their child's food allergy and identify helpful resources.
A total of 40 parents (33 females) participated in the focus groups. Participant demographics were collected. The following 3 main themes emerged: (1) anxiety (an emotional roller coaster); (2) a transformational journey (the waiting game, loss of normalcy, strained relationships and mistrust, and financial challenges); and (3) the need for resources (day to day management, ages and stages, mental health supports, and "the dream").
An in-person allied health care team is needed to provide an integrated, patient-centered approach for how families can live and manage food allergies. Credible information and resources, such as medically reviewed websites, support groups, and counseling services, with a goal of reducing child and parental anxiety, should be provided by health care professionals.
当孩子被诊断出食物过敏时,父母会经历各种情绪,特别是压力和焦虑。管理这种健康状况和应对情绪需要专业和同行的支持。目前,缺乏资源,也缺乏帮助父母管理孩子食物过敏所需的资源的认识。
描述父母在照顾食物过敏儿童时的体验,并回顾父母管理儿童食物过敏所需的资源,更具体地说,了解他们希望这些资源以何种方式提供。
在加拿大不列颠哥伦比亚省共进行了 7 次半结构化焦点小组讨论。要求父母描述他们管理孩子食物过敏的经验,并确定有用的资源。
共有 40 名父母(33 名女性)参加了焦点小组。收集了参与者的人口统计学资料。出现了以下 3 个主要主题:(1)焦虑(情绪过山车);(2)转变之旅(等待游戏、失去常态、紧张的人际关系和不信任、经济挑战);(3)资源需求(日常管理、年龄和阶段、心理健康支持和“梦想”)。
需要一个面对面的医疗保健团队,为家庭提供一种综合的、以患者为中心的方法,帮助他们管理食物过敏。医疗保健专业人员应提供可靠的信息和资源,如经过医学审查的网站、支持小组和咨询服务,以降低儿童和父母的焦虑。