2018
DOI: 10.1002/gps.4965
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Bidirectional relationship between caregiver burden and neuropsychiatric symptoms in patients with Alzheimer's disease: A narrative review

Abstract: Because of the bidirectional relationship between caregiver burden and NPs, the active management strategies of dementia care should include early identification and treatment risk factors for both caregiver stress and NPs in patients with AD. Therefore, to improve one of them can be exert beneficial for the other.

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Cited by 138 publications
(129 citation statements)
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“…Compromised emotional well-being in caregivers (eg, mental disorders) may adversely impact care recipients. There is evidence, for example, that care recipients have poorer general health, mental health, and quality of life and exacerbated disability symptomatology when caregivers experience mental health problems [ 20 , 21 ]. The caregiver burden has also been associated with poorer caregiving quality, including the use of coercive or harmful management techniques, which may damage the relational bond between a caregiver and the care recipient [ 22 - 24 ].…”
Section: Introductionmentioning
confidence: 99%
“…Compromised emotional well-being in caregivers (eg, mental disorders) may adversely impact care recipients. There is evidence, for example, that care recipients have poorer general health, mental health, and quality of life and exacerbated disability symptomatology when caregivers experience mental health problems [ 20 , 21 ]. The caregiver burden has also been associated with poorer caregiving quality, including the use of coercive or harmful management techniques, which may damage the relational bond between a caregiver and the care recipient [ 22 - 24 ].…”
Section: Introductionmentioning
confidence: 99%
“…This observation was supported by a 2-year longitudinal study showing that the burden of caregivers remained stable, and severe depression decreased along with the cognitive, functional, and behavioral worsening of the patients. 17 We aimed to follow for 1 year dyads of patients with AD/ family caregivers selected in clinical case series during the early-middle stages of the disease to evaluate the relationships between anxiety and depression and the burden of caregivers with cognitive, behavioral, and functional deterioration in the patients. Early literature on these topics were not focused on AD dyads, 12,14,15 were not prospective, 11,12 or were obtained by systematic reviews.…”
Section: Introductionmentioning
confidence: 99%
“…The results of the present study support the use of the three subscales of the ZBI namely; embarrassment/ anger, reaction to patients' dependency, and selfcriticism as a measurement of caregiver burden. Isik and colleagues [47], pointed out the fact that caregivers of persons with dementia are experienced more burden and anxiety as compared to caregivers of older adults because they have to cope with both agerelated conditions and dementia related factors, which could worsen the relationship between caregivers and patients [47]. Also, Chiao and colleagues [48] in their provide a positive thinking training intervention among caregivers of persons with dementia to help decrease their burden, which eventually will impact their care recipients challenging behavior.…”
Section: Discussionmentioning
confidence: 99%