Suppr超能文献

雷特综合征脊柱侧弯管理中的父母体验。

Parental experiences of scoliosis management in Rett syndrome.

机构信息

Genetic Services of Western Australia, King Edward Memorial Hospital, Perth, Western Australia.

出版信息

Disabil Rehabil. 2009;31(23):1917-24. doi: 10.1080/09638280902846392.

Abstract

BACKGROUND

Scoliosis is the most common orthopaedic complication of Rett syndrome. Parents of affected individuals are vital partners in the clinical management of scoliosis and this study explored parental experiences of various aspects of different management options.

METHODS

Publicly available Rettnet postings informed the development of an online questionnaire about scoliosis and its management in Rett syndrome. Parents of subjects who met the criteria for Rett syndrome participated in a survey using this questionnaire.

RESULTS

One hundred and eighty families participated in this study with scoliosis having developed in 135 (75.4%) of subjects. Eighty-four (62.2% of subjects with scoliosis) had received specific treatment for scoliosis while 51 (37.8%) had not. Surgery was perceived as improving the scoliosis in the majority of subjects but had considerable emotional effects for families of subjects who were less severely affected (p = 0.055) or older (p = 0.063). Physiotherapy and bracing were perceived as not reducing the progression of the curve, but physiotherapy was frequently reported to be beneficial to the subject's quality of life and bracing was frequently associated with side effects such as decreased mobility and problems with pressure. Only half of respondents felt that information about scoliosis provided by clinicians was adequate.

CONCLUSIONS

The perspectives of parents provided useful insights into the complexities of decision-making regarding scoliosis treatment in Rett syndrome. The provision of scoliosis information by clinicians should be more family-centred.

摘要

背景

脊柱侧凸是雷特综合征最常见的骨科并发症。受影响个体的父母是脊柱侧凸临床管理的重要合作伙伴,本研究探讨了父母对不同管理方案各个方面的经验。

方法

雷特网的公开信息为脊柱侧凸及其在雷特综合征中的管理的在线问卷的制定提供了信息。符合雷特综合征标准的受检者的父母使用该问卷参与了一项调查。

结果

本研究共有 180 个家庭参与,其中 135 名(75.4%)受检者出现了脊柱侧凸。84 名(脊柱侧凸受检者的 62.2%)接受了脊柱侧凸的特定治疗,而 51 名(37.8%)未接受治疗。手术被认为能改善大多数受检者的脊柱侧凸,但对病情较轻(p = 0.055)或年龄较大(p = 0.063)的受检者家庭有较大的情绪影响。物理疗法和支具被认为不能减缓曲线的进展,但物理疗法经常被报告对受检者的生活质量有益,支具经常与活动受限和压力相关问题等副作用相关。只有一半的受访者认为临床医生提供的脊柱侧凸信息足够充分。

结论

父母的观点为了解雷特综合征脊柱侧凸治疗决策的复杂性提供了有用的见解。临床医生提供脊柱侧凸信息时应更加以家庭为中心。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验