Caregiver burden in familial caregivers and foreign domestic workers of patients with traumatic brain injury in a multi-ethnic Asian population

Brain Injury ◽  
2020 ◽  
Vol 34 (11) ◽  
pp. 1513-1517
Author(s):  
Matthew Tay ◽  
Keng He Kong
2016 ◽  
Vol 53 (6) ◽  
pp. 681-692 ◽  
Author(s):  
Karen L. Saban ◽  
Joan M. Griffin ◽  
Amanda Urban ◽  
Marissa A. Janusek ◽  
Theresa Louise-Bender Pape ◽  
...  

Author(s):  
Kirsten Lieshout ◽  
Joanne Oates ◽  
Anne Baker ◽  
Carolyn A. Unsworth ◽  
Ian D. Cameron ◽  
...  

This study examined the patterns of informal (unpaid) caregiving provided to people after moderate to severe traumatic brain injury (TBI), explore the self-reported burden and preparedness for the caregiving role, and identify factors predictive of caregiver burden and preparedness. A cross-sectional cohort design was used. Informal caregivers completed the Demand and Difficulty subscales of the Caregiving Burden Scale; and the Mutuality, Preparedness, and Global Strain subscales of the Family Care Inventory. Chi-square tests and logistic regression were used to examine the relationships between caregiver and care recipient variables and preparedness for caregiving. Twenty-nine informal caregivers who reported data on themselves and people with a moderate to severe TBI were recruited (referred to as a dyad). Most caregivers were female (n = 21, 72%), lived with the care recipient (n = 20, 69%), and reported high levels of burden on both scales. While most caregivers (n = 21, 72%) felt “pretty well” or “very well” prepared for caregiving, they were least prepared to get help or information from the health system, and to deal with the stress of caregiving. No significant relationships or predictors for caregiver burden or preparedness were identified. While caregivers reported the provision of care as both highly difficult and demanding, further research is required to better understand the reasons for the variability in caregiver experience, and ultimately how to best prepare caregivers for this long-term role.


Brain Injury ◽  
1998 ◽  
Vol 12 (12) ◽  
pp. 1045-1059 ◽  
Author(s):  
NIGEL V. MARSH ◽  
DENYSE A. KERSEL ◽  
JACK H. HAVILL ◽  
JAMIE W. SLEIGH

2002 ◽  
Vol 24 (4) ◽  
pp. 434-447 ◽  
Author(s):  
Nigel V. Marsh ◽  
Denyse A. Kersel ◽  
Jack H. Havill ◽  
James W. Sleigh

2020 ◽  
Vol 35 (6) ◽  
pp. 926-926
Author(s):  
Burger C ◽  
Berger R ◽  
Sutcliff L ◽  
Hewitt K

Abstract Objective After an individual sustains a severe traumatic brain injury (sTBI), the recovery process continues, as there are often long-standing difficulties in cognitive, behavioral, and physical abilities. People who care for individuals living with sTBI experience unique challenges. The term to best explain these challenges is caregiver burden. More often than not in research, caregiver burden combines stress and the emotional toll with the most challenging behaviors they encounter. This systematic review aims to assess anxiety for sTBI caregivers. Methods A search for recent, peer-reviewed publications was conducted using GALILEO, which encompasses PsychINFO and PubMed, with the terms “caregiver burden,” “care recipient,” “caregiver,” “burden,” “anxiety,” “stress,” “strain,” “traumatic brain injury” which resulted in N = 1,013 total articles. After excluding irrelevant studies lacking anxiety and sTBI, N = 8 articles remained. Results A review of relevant studies revealed many psychosocial factors that contribute to anxiety including perceived stress/strain management, coping style, and level of care. When an individual had a dual diagnosis of sTBI and psychiatric disorder (e.g., depression) combined with behavioral disturbances (e.g., anger), caregivers showed increased anxiety. Similarly, caregivers’ anxiety increased depending on military career, gender, and relationship status. Protective factors for caregivers included social support and psychotherapeutic interventions, specifically brief structured psychoeducation. Conclusions The results of this systematic review highlight the specific challenges sTBI caregivers face and subsequent anxiety. Individuals with sTBI experience adjustment phases post-injury, and the caregivers experience the transitions alongside the survivor. Future research should investigate how to increase caregiver protective factors and manage the impact of caregiver anxiety on individuals with sTBI.


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