이분척추 환아의 어머니가 인식한 질병관리의 어려움: 질적 서술적 접근

Abstract

Purpose: The purpose of the study was to identify and describe the caregiving difficulties that mothers of children with spina bifida experience from their own perspectives. Methods: A qualitative descriptive study was designed. Data were collected from five mini-focus group interviews and four individual interviews using open-ended questions. Nineteen mothers of children with mild spina bifida participated in the study during 2014-2015. Data were analyzed using qualitative content analysis to identify major difficulties perceived by the mothers. Results: Five domains were identified with 12 subdomains. Daily routine continence management describes difficulties arising in bladder and bowel management for the child with spina bifida. Management of school life of child deals with difficulties in relation to the school facilities, such as the toilets, as well as teachers and friends. Relationship with family and neighbors illustrates problems in relations with their spouse, normal children, relatives and neighbors. Maintaining physical and psychological health includes physical and psychological problems of the mothers. Finance describes economic burden that the mothers face in the management of childs illness. Conclusion: The findings from this study provide insight into the practical issues related to the management of chronic conditions of children with spina bifida from the mothers perspectives.