首页> 美国卫生研究院文献>Dentistry Journal >Experiences of Being a Parent to a Child with Amelogenesis Imperfecta
【2h】

Experiences of Being a Parent to a Child with Amelogenesis Imperfecta

机译:做为不孕症的孩子的父母的经验

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

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.
机译:牙釉质发育不全(AI)是一种遗传性发育障碍,影响牙齿的珐琅质。受影响的患者表现出牙齿过敏,牙齿快速磨损或牙釉质破裂以及颜色和形状改变,所有这些都会损害美观和咀嚼功能。童年时期的慢性病严重影响了整个家庭,影响了正常的家庭常规和/或增加了家庭的经济负担。这项研究的目的是探讨严重的牙釉质发育不全儿童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对心理学家的采访。转录的访谈采用主题分析法进行分析。父母谈到了有关生一个人工智能孩子的几个问题。访谈中出现了四个主要主题:与遗传性疾病的传承相关的感觉,知识减少了压力,对诊断的不熟悉以及社会心理压力。在这些主要类别中,我们确定了几个子主题。与遗传性疾病传承相关的感觉包括内/羞愧这一副主题。减轻压力的知识包括家庭诊断知识和牙科保健专业人员的支持;对诊断的不熟悉包括:漏诊,担心得不到正确的治疗以及疼痛控制不足;最终,心理社会压力这一子主题包括害怕孩子被欺负和紧急牙科就诊。研究结果表明,患有严重牙釉质发育不全的儿童的父母报告的经历与患有其他慢性和罕见疾病的儿童的父母相似。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号