Abstract
The purpose of this study was to identify stressors for visiting nurses supporting the end-of-life of older people
with dementia who are living at home and their families. Study participants included 19 visiting nurses with more
than four years of experience in visiting nursing and end-of-life care for older people with dementia who were
living at home. Narrative data from nurse respondents were collected through semi-structured interviews and
analyzed using qualitative descriptive research methods. Nurses’ narratives about the difficulties, anxieties, and
burdens they experienced in supporting of older people and their families were coded and categorized according to
similar phrases.
Based on the results, 10 categories and 29 subcategories were extracted as stressors. The 10 categories follow:
“Responding to difficulties in daily living due to cognitive decline,” “Older people with dementia living at
home and having difficulty understanding nursing interventions ,”
“Emotionally unstable behavior of the older
people with dementia and their families,” “Difficulties helping family members accept dementia,” “Addressing
the difficulty of bearing the costs of reviewing home health and nursing care,” “Difficulty supporting family
members who make decisions on their behalf,” “Family confusion conceming end-of-life care for older people
with dementia who cannot communicate,” “Difficulties in multidisciplinary cooperation,” “Fatigue due to
busy schedules with multiple tasks,” and “Lack of knowledge and skills necessary for a wide range of nursing
practices.”
The similarities and relationships among the stressors of visiting nurses were examined, and the results were
classified into four categories: difficulty coping with core and peripheral symptoms associated with dementia,
difficulties with continuing home care, difficulty supporting family members at the end of life, and task-oriented
difficulties in visiting nursing. These four perspectives of stressors suggest visiting nurses’ need to cope with
stress.