利用定向内容分析探讨Rett综合征患者口腔健康相关的生活质量

IF 1.7 4区 生物学 Q3 GENETICS & HEREDITY
Yvonne Yee Lok Lai, Jenny Anne Downs, Helen Margaret Leonard, Laurence James Walsh, Sobia Zafar
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引用次数: 0

摘要

目前还没有有效的口腔健康相关生活质量(OHRQOL)仪器用于严重智力和发育障碍以及非语言交流的患者。本定性研究旨在探讨对Rett综合征(RTT)患者口腔健康相关生活质量重要的领域。2021年,在有目的抽样之后,对澳大利亚RTT数据库中证实MECP2突变的个体的父母进行了记录访谈(n = 31)。访谈问题包括口腔问题的经历、他们女儿的口腔健康对她生活的其他方面、对他人生活以及对家庭生活质量的影响。进行定向内容分析。围绕口腔健康对儿童的影响确定了七个领域——不适、疼痛、饮食、日常生活活动、情绪健康、社会健康和提供服务——对患者的影响。五个与家庭影响相关的领域-情绪,活动,家庭功能,冲突,士气和自我效能促进口腔保健。本研究的发现为RTT患者制定有针对性的OHRQOL测量方法铺平了道路,以了解和测量口腔健康的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exploring Oral Health Related Quality of Life in Rett Syndrome Using Directed Content Analysis.

No validated oral health-related quality of life (OHRQOL) instrument currently exists for those with severe intellectual and developmental disabilities and who communicate non-verbally. This qualitative study aimed to explore the domains that were important to the oral health-related quality of life in individuals with Rett syndrome (RTT). In 2021, following purposive sampling, recorded interviews were conducted with parents of individuals with a confirmed MECP2 mutation in the Australian RTT database (n = 31). Interview questions covered experiences of oral problems, the impacts of their daughter's oral health on other aspects of her life and on the lives of others, and on the family's quality of life. Directed content analysis was conducted. Seven domains were identified around the impacts of oral health on the child- discomfort, pain, eating, activities of daily living, emotional well-being, social well-being, and provision of services- affecting impacts on the patient. Five domains related to impacts on the family- emotions, activities, family function, conflict, and morale and self-efficacy to facilitate oral healthcare. The findings of this study pave the way for developing targeted OHRQOL measures for patients with RTT to understand and measure oral health impacts.

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来源期刊
CiteScore
3.50
自引率
5.00%
发文量
432
审稿时长
2-4 weeks
期刊介绍: The American Journal of Medical Genetics - Part A (AJMG) gives you continuous coverage of all biological and medical aspects of genetic disorders and birth defects, as well as in-depth documentation of phenotype analysis within the current context of genotype/phenotype correlations. In addition to Part A , AJMG also publishes two other parts: Part B: Neuropsychiatric Genetics , covering experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. Part C: Seminars in Medical Genetics , guest-edited collections of thematic reviews of topical interest to the readership of AJMG .
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