Anderson Rebecca, Walburn Jessica, Morgan Myfanwy
King's College London, London, United Kingdom.
Qual Health Res. 2020 Jul;30(8):1275-1286. doi: 10.1177/1049732319826561. Epub 2019 Feb 9.
In this study, we examine photoprotection for children with Xeroderma pigmentosum (XP), a rare genetic skin disease requiring rigorous photoprotection, to reduce risks of severe burning and skin cancers from exposure to ultraviolet radiation (UVR). We elicit the views and experiences of both children and their parents to inform the care and support provided. Qualitative semistructured interviews were undertaken with 12 child-parent dyads recruited from the National XP Specialist service in London. We employed a framework approach to analysis. This identified a high level of photoprotection based either on "protection" to facilitate normal activities or "avoidance" of outdoor activity with priority given to normality in the future. These approaches were shaped by perceptions of clinical risk, the emphasis given to a normal family life and families' circumstances and resources. The findings contribute to notions of normalization and coping with demanding care regimens and inform approaches to working with families.
在本研究中,我们探讨了对患有着色性干皮病(XP)儿童的光保护措施。XP是一种罕见的遗传性皮肤病,需要严格的光保护,以降低因暴露于紫外线辐射(UVR)而导致严重晒伤和皮肤癌的风险。我们征集了儿童及其父母的观点和经历,以为所提供的护理和支持提供参考。对从伦敦国家XP专科服务机构招募的12对儿童-父母进行了定性半结构化访谈。我们采用了框架分析法。这确定了基于“保护”以促进正常活动或“避免”户外活动的高水平光保护措施,其中优先考虑未来的正常状态。这些方法受到对临床风险的认知、对正常家庭生活的重视以及家庭情况和资源的影响。研究结果有助于形成正常化观念和应对苛刻护理方案的方法,并为与家庭合作的方式提供参考。