Home care nursing challenges in caregiver burden in Alzheimer’s patients home care settings.
Tamang, Salina (2025)
Tamang, Salina
2025
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Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:amk-2025120432648
https://urn.fi/URN:NBN:fi:amk-2025120432648
Tiivistelmä
The Alzheimer disease is a global health crisis depriving over 55 million people, and the figure will be
acutely increasing. With the movement to home environments, care is becoming a heavy burden on both
professional and professional provision care providers. They are usually untrained, emotionally drained,
and working on vague roles. Families are also isolated by stigma and shame in most cultures and slow to
support. The complex behavioral, safety, and communicative demands of the disease increase these challenges.
This paper sought to conduct a methodological review of literature available on the experiences of nurses
and unpaid caregivers in Alzheimer home care. Two databases, CINAHL and PubMed, with the studies published from 2011 to 2025, were used to collect data. There were 250 screened articles, and seven peer-reviewed articles that fit in with the inclusion criteria. Analysis of the chosen studies was done through traditional content analysis. Three distinct areas were the emotional weight of caregiving, logistic problems with
home caregiving, and structural issues related to quality of care
In Conclusion, emotional burdens (stress, guilt, and isolation due to unending care) practical issues (lack of
personnel, unsafe conditions, and poorly defined protocols) and systemic barriers (fragmented healthcare,
stigma, and financial restraints) were the three major areas of challenges found. The solutions to these will
demand nurse-specific training in dementia, more institutional support, and culturally appropriate family
education, and additional research will be needed in scalable solutions in low-resource environments.
acutely increasing. With the movement to home environments, care is becoming a heavy burden on both
professional and professional provision care providers. They are usually untrained, emotionally drained,
and working on vague roles. Families are also isolated by stigma and shame in most cultures and slow to
support. The complex behavioral, safety, and communicative demands of the disease increase these challenges.
This paper sought to conduct a methodological review of literature available on the experiences of nurses
and unpaid caregivers in Alzheimer home care. Two databases, CINAHL and PubMed, with the studies published from 2011 to 2025, were used to collect data. There were 250 screened articles, and seven peer-reviewed articles that fit in with the inclusion criteria. Analysis of the chosen studies was done through traditional content analysis. Three distinct areas were the emotional weight of caregiving, logistic problems with
home caregiving, and structural issues related to quality of care
In Conclusion, emotional burdens (stress, guilt, and isolation due to unending care) practical issues (lack of
personnel, unsafe conditions, and poorly defined protocols) and systemic barriers (fragmented healthcare,
stigma, and financial restraints) were the three major areas of challenges found. The solutions to these will
demand nurse-specific training in dementia, more institutional support, and culturally appropriate family
education, and additional research will be needed in scalable solutions in low-resource environments.
