Research Fellow in Skin Health and Dermatology Care, School of Health Care, Faculty of Medicine and Health, University of Leeds, Leeds, UK.
Professor in Clinical Nursing Research. Department of Health Sciences, University of York, Heslington, York, UK.
Int J Dermatol. 2017 Dec;56(12):1432-1437. doi: 10.1111/ijd.13785. Epub 2017 Oct 23.
INTRODUCTION/BACKGROUND: Mycobacterium ulcerans (also known as Buruli ulcer) disease is a rare skin disease which is prevalent in rural communities in the tropics mostly in Africa. Mortality rate is low, yet morbidity and consequent disabilities affect the quality of life of sufferers.
The aim of this paper is to use the grounded theory method to explore the support needs of people living with the consequences of Buruli ulcer in an endemic rural community in Ghana.
We used the grounded theory research approach to explore the experiences of people living with Mycobacterium ulcerans in a rural district in Ghana and provide a basis to understand the support needs of this group.
The key support needs identified were: functional limitations, fear and frequency of disease recurrence, contracture of limbs and legs, loss of sensation and numbness in the affected body area, lack of information from health professionals about self-care, feeling tired all the time, insomnia, lack of good diet, lack of access to prostheses, having to walk long distances to access health services, and loss of educational opportunities.
The study discusses how the systematically derived qualitative data has helped to provide a unique insight and advance our understanding of the support needs of people living with BU and how they live and attempt to adapt their lives with disability. We discuss how the availability of appropriate interventions and equipment could help them self-manage their condition and improve access to skin care services.
The support needs of this vulnerable group were identified from a detailed analysis of how those living with BU coped with their lives. A key issue is the lack of education to assist self-management and prevent deterioration. Further research into the evaluation of interventions to address these support needs is necessary including self-management strategies.
简介/背景:溃疡分枝杆菌(也称为伯里溃疡)病是一种罕见的皮肤疾病,主要在非洲的热带农村社区流行。死亡率较低,但发病率和随之而来的残疾会影响患者的生活质量。
本文旨在使用扎根理论方法探讨在加纳一个流行地区农村社区中患有伯里溃疡后果的人的支持需求。
我们使用扎根理论研究方法来探讨生活在加纳农村地区的人患有溃疡分枝杆菌的经历,并为了解这一人群的支持需求提供基础。
确定的主要支持需求包括:功能受限、对疾病复发的恐惧和频率、四肢和腿部挛缩、受影响身体区域的感觉丧失和麻木、缺乏卫生专业人员关于自我护理的信息、一直感到疲倦、失眠、饮食不良、无法获得义肢、需要走很长的路才能获得医疗服务以及失去受教育机会。
该研究讨论了如何从系统地得出的定性数据中获得独特的见解,并深入了解患有 BU 的人的支持需求,以及他们如何生活并试图适应残疾生活。我们讨论了适当的干预措施和设备的可用性如何帮助他们自我管理病情并改善获得皮肤护理服务的机会。
从患有 BU 的人应对生活的详细分析中确定了这些弱势群体的支持需求。一个关键问题是缺乏教育来协助自我管理和防止病情恶化。需要进一步研究评估干预措施以满足这些支持需求,包括自我管理策略。