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首页> 外文期刊>Orphanet journal of rare diseases >Occupational therapy for epidermolysis bullosa: clinical practice guidelines
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Occupational therapy for epidermolysis bullosa: clinical practice guidelines

机译:大疱表皮松解症的职业治疗:临床实践指南

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Abstract The purpose of this article is to summarize the Dystrophic Epidermolysis Bullosa Research Association (DEBRA) International evidence-based Clinical Practice Guidelines (CPGs) for the provision of occupational therapy (OT) for children and adults living with inherited epidermolysis bullosa (EB). This is a rare genetic disorder characterized by skin fragility leading to blister formation occurring spontaneously or following minor trauma. Current OT practice for persons with EB is based on anecdotal care, clinical expertise and trial and error with collaboration between caregiver and patient. Intervention based on research is needed to establish a foundation of knowledge to guide international practitioners to create and improve standards of care and to be able to work effectively with those living with the rare diagnosis of this condition.This CPG was created by an international panel with expertise working with persons with EB. The panel was made up of 11 members including OT’s, a physiotherapist, a medical doctor, social worker, person with EB and a carer of a person with EB. It describes the development of recommendations for 5 outcomes determined by survey of persons with EB, caregivers, and experienced healthcare professionals. The outcomes include independence in activities of daily living (ADL), independence in instrumental ADL, maximization of hand function (non-surgical), fine motor development and retention, and oral feeding skills. The recommendations are supplemented with additional files that include photos and specific examples to further guide occupational therapists or, in situations where an OT is not available, other members of the healthcare team.As the disorder of EB is rare, evidence-based CPGs are needed to provide a base of knowledge and practice for OTs throughout the world with the goal of providing quality care to patients, while improving their functional independence and quality of life. In addition, this information is valuable as a basis for further research.
机译:摘要本文旨在总结营养不良性大疱性表皮松解研究协会(DEBRA)的国际循证临床实践指南(CPG),为患有遗传性大疱性表皮松解(EB)的儿童和成人提供职业治疗(OT)。这是一种罕见的遗传病,其特征是皮肤脆弱,导致水疱形成,自然而然或在受到轻微创伤后发生。当前针对EB患者的OT实践基于轶事护理,临床专业知识以及护理人员与患者之间协作的反复试验。需要以研究为基础的干预措施,以建立知识基础,以指导国际从业者创建和改善护理标准,并能够与患有这种疾病的罕见诊断者有效地合作。与EB人员合作的专业知识。该小组由11名成员组成,其中包括OT,物理治疗师,医生,社会工作者,患有EB的人和患有EB的人的照料者。它描述了通过对EB患者,看护者和有经验的医疗保健专业人员进行调查而确定的针对5种结果的建议的制定。结果包括日常生活活动(ADL)的独立性,工具性ADL的独立性,手功能的最大化(非手术),精细的运动发育和保持能力以及口服喂养技巧。在建议的基础上增加了一些文件,其中包括照片和特定示例,以进一步指导职业治疗师,或者在无法提供OT的情况下,医疗团队的其他成员。由于EB病很罕见,因此需要循证CPG为全世界的OT提供基础知识和实践,目的是为患者提供优质的护理,同时改善他们的功能独立性和生活质量。另外,这些信息作为进一步研究的基础是有价值的。

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