C.-Y. Chiao’s scientific contributions

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Publications (1)


Caregiver burden for informal caregivers of patients with dementia: A systematic review: Caregiver burden for informal caregivers
  • Article

June 2015

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1,039 Reads

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674 Citations

International Nursing Review

C.-Y. Chiao

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H.-S. Wu

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C.-Y. Hsiao

Background: Dementia is an irreversible illness. The caregiver is expected to assume increased responsibility as the condition of the person with dementia declines. It is important to explore the factors constituting caregiver burden on the informal caregivers of people with dementia. Aims: The purpose of this article is to identify the factors constituting caregiver burden on the informal caregivers of people with dementia living in the community. Methods: A systematic review of the four databases, including PubMed, PsycINFO, CINAHL and the Cochrane Library, was carried out to access relevant articles published between 2003 and 2012. Twenty-one articles met the inclusion criteria of this study. Results: Behavioural problems or psychological symptoms were the primary factor of the person with dementia that is associated with caregiver burden. Caregiver socio-demographical factors and psychological factors were the two primary factors of the caregiver burden. Limitations: Several results of this study were based on studies that had their own limitations. Furthermore, the concept of caregiver 'burden' was not clearly defined in some of the studies; instead, the term was broadly defined. Conclusion: Factors of caregiver burden in regard to people with dementia living in the community were clarified in this review study. By identifying all of the factors, healthcare professionals can deliver appropriate assistance to relieve caregiver burden and improve the quality of caregiving for people with dementia. Implications for nursing and health policy: It is important to identify the factors of the burden on the caregivers of people with dementia living in the community to prevent early nursing home placement, deterioration of caregiver's health and reduce the adverse health outcomes for care recipients. A health-related policy should be formulated to help informal caregivers receive more professional assistance. Training opportunities should be provided for family caregivers to reduce the impact of caregiving on the delivery of effective care.

Citations (1)


... Caregiver burden is a complex, multidimensional concept defined as an individual's response to challenges they face when providing care for a sick family member [13]. It is well described for caregivers of people with dementia [14,15], and a clinical level of burden is reported in 50% owners of pets with terminal diseases [16] and 16% of caregivers of dogs suffering from CCD [17]. One of its implications is reduced adherence to the treatment plan and, hence, deterioration in disease management. ...

Reference:

Attitudes of Australian Veterinary Professionals to Diagnosing and Managing Canine Cognitive Dysfunction
Caregiver burden for informal caregivers of patients with dementia: A systematic review: Caregiver burden for informal caregivers
  • Citing Article
  • June 2015

International Nursing Review