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      The effects of caregiver's burden on dynamic structure in disorder of consciousness families: An observational study

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          Abstract

          Introduction

          Disorder of consciousness is a clinical condition due to severe brain damage. The impact of consciousness disorder on the family is characterized by a combination of biopsychosocial factors. The burden and suffering perceived by caregivers can cause psychological distress characterized by anxiety, depression, and physical illness. The aim of the study was to investigate the interaction between family dynamics and caregiver burden.

          Methods

          We enlisted 35 caregivers of subjects in a minimally conscious state. Two skilled psychologists administered the Olson's Adaptability and Family Cohesion Assessment Scale and the Novak's Burden Inventory Caregiver Scale to assess family function and family burden, respectively.

          Results

          We found that the caregiver burden correlates with the family adaptability and cohesion, as well as with enmeshment, rigidity, and disengagement.

          Conclusion

          Findings suggest that the traumatic event does not affect the family structure. Families are able to maintain a balanced functioning and control distress.

          Abstract

          Disorder of consciousness is a clinical condition due to severe brain damage. The burden and suffering perceived by caregivers can cause psychological distress characterized by anxiety, depression and physical illness. The patient and his/her family should be followed by a multidisciplinary team including a neuropsychologist, who can facilitate the family dynamic structure and to safeguard the welfare of the patient.

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          Most cited references26

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          Application of a multidimensional caregiver burden inventory.

          Multidimensional measures of caregiver burden give a sensitive reading of caregivers' feelings and a sophisticated picture of caregivers' responses to the demands of care. This paper reports on the development of a 24-item, five-subscale Caregiver Burden Inventory (CBI) and demonstrates its use as a diagnostic tool for professional caregivers. It concludes with a discussion of several ways that professional caregivers can use this multidimensional measure of caregiver burden.
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            Predictors of caregiver burden in caregivers of individuals with dementia.

            This article is a report on a study of the multidimensional predictors of caregiver burden in caregivers of individuals with dementia using nationally representative data. Caregiver burden affects the health of both caregivers and their care-recipients. Although previous studies identified various predictors of caregiver burden, these predictors have not been confirmed in nationally representative population. Data for this secondary analysis was provided by the National Alliance for Caregiving, American Association of Retired Persons. The data were collected through a telephone survey of randomly selected adults in seven states in 2003 (weight adjusted n = 302). Descriptive statistics, inter-correlation analysis and a hierarchical multiple regression analysis were performed. Disease-related factors were the most significant predictors, explaining 16% of caregiver burden; these were followed by caregiver socio-demographical factors and caregiving-related factors (F = 21·28, P < 0·01). Significant individual predictors were impairment of activities of daily living or instrumental activities of daily living, the number of hours of caregiving, use of coping strategies, co-residence, spousal status and caregiver gender (P < 0·05). Impaired function in care-recipients predicts caregiver burden, and also interacts with demographical- and caregiving-related factors. Thus, it will be beneficial to both care-recipients and caregivers to target nursing interventions and community services to improve the functional abilities of individuals with dementia. © 2011 The Authors. Journal of Advanced Nursing © 2011 Blackwell Publishing Ltd.
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              Impact of caregiving on health and quality of life: a comparative population-based study of caregivers for elderly persons and noncaregivers.

              This study aims to investigate the impact of caregiving on the health status and quality of life (QOL) of primary informal caregivers (PCGs) of elderly care recipients in Hong Kong. A total of 246 PCGs and 492 matched noncaregiver (NCG) controls were identified in a population-based cross-sectional study through random telephone dialing. Their health status and QOL were assessed based on structured questionnaires and Short Form 36 (SF-36) Health Survey. Multiple conditional logistic regression analysis showed that compared with NCGs, PCGs had significantly increased risks for reporting worse health, more doctor visits, anxiety and depression, and weight loss. Female PCGs were more likely to report chronic diseases, symptoms, and insomnia. PCGs, particularly women, had significantly lower scores in all eight domains of SF-36 Health Survey. High caregiver burden score (Zarit Burden Scale) was positively associated with adverse physical and psychological health and poorer QOL. The results indicate that PCGs, particularly women, had an adverse physical and psychological health profile and poorer QOL compared with NCGs.
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                Author and article information

                Contributors
                mariacristina.decola@irccsme.it
                Journal
                Brain Behav
                Brain Behav
                10.1002/(ISSN)2157-9032
                BRB3
                Brain and Behavior
                John Wiley and Sons Inc. (Hoboken )
                2162-3279
                05 August 2021
                August 2021
                : 11
                : 8 ( doiID: 10.1002/brb3.v11.8 )
                : e2305
                Affiliations
                [ 1 ] IRCCS Centro Neurolesi “Bonino‐Pulejo” Messina Italy
                Author notes
                [*] [* ] Correspondence

                Maria Cristina De Cola, IRCCS Centro Neurolesi “Bonino‐Pulejo”, Via Palermo S.S. 113, C.da Casazza 98124 Messina, Italy.

                Email: mariacristina.decola@ 123456irccsme.it

                Author information
                https://orcid.org/0000-0003-4862-3832
                https://orcid.org/0000-0002-7509-3833
                Article
                BRB32305
                10.1002/brb3.2305
                8413804
                34350729
                093163ea-d10c-4fc2-a19b-676cb2ce645b
                © 2021 The Authors. Brain and Behavior published by Wiley Periodicals LLC

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 22 June 2021
                : 25 March 2021
                : 12 July 2021
                Page count
                Figures: 2, Tables: 2, Pages: 6, Words: 3500
                Funding
                Funded by: Italian Health Minister
                Award ID: GR‐2013‐02359341
                Categories
                Original Research
                Original Research
                Custom metadata
                2.0
                August 2021
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.0.6 mode:remove_FC converted:03.09.2021

                Neurosciences
                caregivers,disorders of consciousness,minimally conscious state,psychological function

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