Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

1
25
0

Year Published

2020
2020
2023
2023

Publication Types

Select...
7

Relationship

0
7

Authors

Journals

citations
Cited by 21 publications
(26 citation statements)
references
References 50 publications
1
25
0
Order By: Relevance
“…23 Caring for someone with dementia is a complex, multidisciplinary task requiring the involvement of families, healthcare professionals, and social services and generates higher levels of stress and anxiety than caring for patients with other chronic disabling diseases. 25,26 In our study, a total of 42 (9.4%) participants reported being informal caregivers of first-degree relatives with AD. They showed a better knowledge of AD compared with non-caregivers as measured by the ADKS.…”
Section: Discussionmentioning
confidence: 63%
“…23 Caring for someone with dementia is a complex, multidisciplinary task requiring the involvement of families, healthcare professionals, and social services and generates higher levels of stress and anxiety than caring for patients with other chronic disabling diseases. 25,26 In our study, a total of 42 (9.4%) participants reported being informal caregivers of first-degree relatives with AD. They showed a better knowledge of AD compared with non-caregivers as measured by the ADKS.…”
Section: Discussionmentioning
confidence: 63%
“…The need for high quality caregiving is likewise escalating concomitantly. After diagnosis, persons with AD typically live an average of 4–8 years, and some up to 20 years ( Kokorelias et al, 2020 ). The shortage of medical specialists for ADRD places a great burden on primary care providers, who feel ill-equipped and undertrained to advise or treat this patient population ( Peterson et al, 2016 ; Bernstein et al, 2019 ; Kistler et al, 2020 ).…”
Section: The Problemmentioning
confidence: 99%
“…When persons with AD remain at home, the informal caregiver (i.e., family members) sustain increasing responsibility and challenges in caring for the basic needs of their loved ones ( Lee et al, 2019b ). These caregivers have “unmet needs for general information regarding Alzheimer’s disease, tangible care services, respite, and emotional and financial support, and learning skills for improving daily care management” ( Kokorelias et al, 2020 , p. 2). Females in particular seem to experience more family conflict, depression, and distress compared to male during the time of transition to caregiver role ( Lee et al, 2019b ).…”
Section: Caregiversmentioning
confidence: 99%
See 2 more Smart Citations