Support needs of people living with Mycobacterium ulcerans (Buruli ulcer) disease in a Ghana rural community: a grounded theory study. (23rd October 2017)

• Record Type: Journal Article
• Authors: Effah, Alex; Ersser, Steven J.; Hemingway, Ann
• Is Part Of: International journal of dermatology. Volume 56:Number 12(2017)
• Page Start: 1432
• Page End: 1437
• Publication Date: 2017-10-23
• Subjects: Dermatology -- Periodicals; 616.5
• DOI: 10.1111/ijd.13785
• Languages: English
• ISSNs: 0011-9059

Abstract

Abstract: 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. Aims: 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. Methods: 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. Results: 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. Discussions: 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. Conclusions: 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.