Pousette Lundgren Gunilla, Hasselblad Tove, Johansson Anna Stigsdotter, Johansson Anna, Dahllöf Göran
Division of Orthodontics and Pediatric Dentistry, Department of Dental Medicine, Karolinska Institutet POB 4064, SE-141 04 Huddinge, Sweden.
Center for Pediatric Oral Health Research, SE-171 77 Stockholm, Sweden.
Dent J (Basel). 2019 Feb 9;7(1):17. doi: 10.3390/dj7010017.
Amelogenesis imperfecta (AI) is a hereditary developmental disorder affecting the enamel of teeth. Affected patients present with tooth hypersensitivity, rapid tooth wear, or fractures of enamel as well as alterations in color and shape, all of which compromise esthetic appearance and masticatory function. Chronic conditions in childhood severely impact the whole family, affecting normal family routines and/or increasing the family's financial burden. The aim of this study was to explore experiences and the impact on daily life of being a parent to a child with severe forms of amelogenesis imperfecta. Parents of children and adolescents with AI participated in an interview with a psychologist. The transcribed interviews were analyzed using thematic analysis. The parents talked about several concerns about having a child with AI. Four main themes emerged from the interviews: Feelings associated with passing on a hereditary disorder, knowledge decreases stress, unfamiliarity with the diagnosis, and psychosocial stress. In these main categories we identified several subthemes. Feelings associated with passing on a hereditary disorder included the subtheme of guilt/shame; knowledge decreases stress included knowledge about diagnosis in the family and support from dental health care professionals; Unfamiliarity with diagnosis included missed diagnosis, fear of not getting correct treatment, and insufficient pain control; finally, the subtheme Psychosocial stress included fear of child being bullied and emergency dental visits. The findings show that parents of children with severe amelogenesis imperfecta report similar experiences as do parents of children with other chronic and rare diseases.
釉质发育不全(AI)是一种影响牙齿釉质的遗传性发育障碍。受影响的患者表现出牙齿过敏、牙齿快速磨损或釉质骨折以及颜色和形状的改变,所有这些都会损害美观和咀嚼功能。儿童时期的慢性病会严重影响整个家庭,影响正常的家庭日常生活和/或增加家庭的经济负担。本研究的目的是探讨作为患有严重形式釉质发育不全孩子的父母的经历及其对日常生活的影响。患有AI的儿童和青少年的父母参加了与心理学家的访谈。对转录的访谈采用主题分析法进行分析。父母们谈到了对患有AI孩子的几个担忧。访谈中出现了四个主要主题:与遗传疾病遗传相关的感受、知识减少压力、对诊断不熟悉以及心理社会压力。在这些主要类别中,我们确定了几个子主题。与遗传疾病遗传相关的感受包括内疚/羞耻子主题;知识减少压力包括家庭中关于诊断的知识以及来自牙科保健专业人员的支持;对诊断不熟悉包括漏诊、担心得不到正确治疗以及疼痛控制不足;最后,心理社会压力子主题包括担心孩子被欺负和紧急牙科就诊。研究结果表明,患有严重釉质发育不全孩子的父母所报告的经历与患有其他慢性和罕见疾病孩子的父母类似。