The relationship between psychiatric patients’ caregiver burden and anger expression styles

Yıldırım, Serap; Akyüz, Özge; Engin, Esra; Gültekin, Kadriye

doi:10.1111/jocn.14060

Cited by 4 publications

(2 citation statements)

References 12 publications

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“…The scientific literature associates an increase in burden with certain degrees of kinship at the sociodemographic level, such as being a spouse or mother (Alexander et al, 2016;Lasebikan & Ayinde, 2013). In addition, the patient's symptomatic behavior can be influential (Yildirim et al, 2018), as well as a recent hospitalization (Foldemo et al, 2005;Lloyd et al, 2011;Möller-Leimkühler, 2005), a high number of relapses (Alexander et al, 2016), financial problems (Zivin et al, 2013), infrequent social and occupational contact of the patient (Gutiérrez-Maldonado et al, 2012) or cultural aspects (Awad & Voruganti, 2008), among others. This whole set of situations can favor the tendency of the appearance of the so-called caregiver syndrome.…”

Section: Introductionmentioning

confidence: 99%

The impact of community care: Burden and quality of life of the informal caregivers of patients with severe mental disorder

Estrada-Fernández

Gil‐Lacruz

Gil-Lacruz

et al. 2021

Journal Community Psychology

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This study analyzes the dimensions and consequences of the burden of caregivers of patients with SMD (Severe Mental Disorder) and the repercussions that this role has on their quality of life and health in the physical, psychic and social spheres. This is a descriptive cross-sectional study and inferential observational study which explores caregivers of patients with SMD admitted to Psychiatry Day Hospital (Huesca, Spain). The technique of consecutive cases was used as a technique for sampling and sample selection. An individualized interview was arranged, where sociodemographic data were collected and scales and instruments were administered. 52 caregivers met the inclusion criteria. The female sex predominates (67%), being the patient's mother (48%). The average age of caregivers is 60 years old. Almost 60% of the sample presents intense burden and alterations of general mental health, 77% reveal anxiety and depression, and 46% little social support.Burden is associated with hospitalization within the last year, anxiety, or total social support received. It is appreciated how the diagnosis of a chronic disease constitutes an important challenge for the patient and their family, dueThis is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

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Section: Introductionmentioning

confidence: 99%

The impact of community care: Burden and quality of life of the informal caregivers of patients with severe mental disorder

Estrada-Fernández

Gil‐Lacruz

Gil-Lacruz

et al. 2021

Journal Community Psychology

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“…The Caregiver Burden Inventory (CBI) is a self-administered, multidimensional scale for assessing caregiver burden among caregivers of persons with dementia [28], children with cancer [29], psychiatric patients [30] and rheumatoid arthritis patients [31]. This measure consists of 24 items divided into ve domains: Timedependence (1 ~ 5 items), developmental burden (6 ~ 10 items), physical burden (11 ~ 14 items), social burden (15 ~ 18 items), and emotional burden (19 ~ 24 items) [32].…”

Section: Caregiver Burden Inventory (Cbi)mentioning

confidence: 99%

The level and factors associated with caregiver burden among parents of children with cerebral palsy: A cross-sectional study in southwest China

Zhong,

Wijesinghe,

et al. 2023

Preprint

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Purpose This study was conducted to determine the level of care burden and its related factors in the parents of children with cerebral palsy (CP). Design and methods This descriptive cross-sectional study was conducted with parents of 165 children with cerebral palsy who were enrolled in children rehabilitation departments of three tertiary hospitals in Chengdu, Sichuan Province between September 2021 and December 2022. Besides demographic information, the Caregiver Burden Inventory (CBI), the Patient Health Questionaire-9 (PHQ-9) and Fatigue Severity Scale (FSS) were used to collect data. Data were analyzed by descriptive and inferential statistics (correlation and multiple linear regressions analysis). Results The mean (± SD) CBI score of the parents was 42.18 ± 18.79. The score of FSS and PHQ-9 demonstrated positive moderate to strong correlations with caregiver burden (r = 0.461, P < 0.001; r = 0.630, P < 0.001, respectively). The results of the multiple linear regressions analysis showed that a low level of education, long caring time and combined visual impairment, higher depression and fatigue had a influence on caregiver burden, and 46.4% of the variance in caregiver burden was explained by these factors. Conclusions The key predictors of caregiver burden include the level of education, caring time, children with visual impairment and the degree of depression and fatigue. Effort should be made to relieve burden in parents of children with cerebral palsy.

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The relationship between caregiver burden and anger level of informal caregivers of patients in palliative care centre

Çatıker,

Uğur,

Bülbül

et al. 2023

Int J Palliat Nurs

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Background: Palliative care is a comprehensive service that includes not only the patient but also the caregivers. Aims: This research was carried out to determine the relationship and factors affecting the burden and anger level of informal caregivers of patients. Methods: This descriptive study was conducted with caregivers (n=206) of patients hospitalised in two Palliative Care Centers in Ordu, Türkiye. Findings: In the research, it was determined that there was a statistically significant relationship between the burden of caregivers and the trait anger level, anger-in, anger-out sub-dimension scores of The Trait Anger and Anger Expression Scale, but a negative relationship was found between the burden of caregivers and anger control sub-dimension scores of The Trait Anger and Anger Expression Scale. Conclusions: The burden of a caregiving process has a positive impact on the trait anger level, anger-in, anger-out but has a negative impact on anger control. Nurses should monitor a caregiver's level of anger and burden and develop programmes required to decrease the caregiver's anger level and burden.

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The relationship between psychiatric patients’ caregiver burden and anger expression styles

Abstract: Knowing the anger expression styles of caregivers is important for reducing caregiver burden and improving quality of care.

Cited by 4 publications

References 12 publications

The impact of community care: Burden and quality of life of the informal caregivers of patients with severe mental disorder

The impact of community care: Burden and quality of life of the informal caregivers of patients with severe mental disorder

The level and factors associated with caregiver burden among parents of children with cerebral palsy: A cross-sectional study in southwest China

The relationship between caregiver burden and anger level of informal caregivers of patients in palliative care centre

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