Department of Rehabilitation, Lucile Packard Children's Hospital Stanford, 321 Middlefield Road, Menlo Park, CA, 94025, USA.
Phoenix Children's Hospital, Phoenix, USA.
Orphanet J Rare Dis. 2019 Jun 7;14(1):129. doi: 10.1186/s13023-019-1059-8.
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.
本文旨在总结 Dystrophic Epidermolysis Bullosa Research Association(DEBRA)国际循证临床实践指南(CPG),为遗传性大疱性表皮松解症(EB)患者提供职业治疗(OT)。这是一种罕见的遗传性疾病,其特征为皮肤脆弱,导致水疱形成,可自发性或轻微创伤后发生。目前针对 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的反复试验。需要基于研究的干预措施来建立知识基础,指导国际从业人员制定和改进护理标准,并能够与那些患有这种罕见疾病的人有效合作。本 CPG 由具有 EB 患者工作经验的国际专家组创建。该专家组由 11 名成员组成,包括 OT、物理治疗师、医生、社会工作者、EB 患者和 EB 患者的护理人员。它描述了通过对 EB 患者、护理人员和经验丰富的医疗保健专业人员进行调查确定的 5 项结果的建议制定过程。这些结果包括日常生活活动(ADL)的独立性、工具性 ADL 的独立性、手部功能(非手术)最大化、精细运动发展和保留以及口腔喂养技能。建议还附有其他文件,包括照片和具体示例,以进一步指导 OT 或在没有 OT 的情况下,指导其他医疗保健团队成员。由于 EB 疾病罕见,因此需要循证 CPG 为世界各地的 OT 提供知识和实践基础,以目标为为患者提供优质护理,同时提高他们的功能独立性和生活质量。此外,这些信息作为进一步研究的基础具有重要价值。