scholarly journals Caregiving motivations and experiences among family caregivers of patients living with advanced breast cancer in Ghana

PLoS ONE ◽  
2020 ◽  
Vol 15 (3) ◽  
pp. e0229683 ◽  
Author(s):  
Grace Kusi ◽  
Adwoa Bemah Boamah Mensah ◽  
Kofi Boamah Mensah ◽  
Veronica Millicent Dzomeku ◽  
Felix Apiribu ◽  
...  
2004 ◽  
Vol 19 (2) ◽  
pp. 139-155 ◽  
Author(s):  
Trace Kershaw ◽  
Laurel Northouse ◽  
Charuwan Kritpracha ◽  
Ann Schafenacker ◽  
Darlene Mood

Author(s):  
Ikechi E. Jite ◽  
Adedotun A. Adetunji ◽  
Ayorinde M. Folasire ◽  
Joshua O. Akinyemi ◽  
Segun Bello

Background: The responsibility of caring for patients with advanced cancer in sub-Saharan Africa is mostly shouldered by family members because of paucity of institutional facilities. There is a growing concern that the number of women needing treatment for advanced breast cancer is rising at an unprecedented rate in Nigeria.Aim: To assess the caregiver burden and its associated factors amongst family caregivers of women with advanced breast cancer.Setting: The study was conducted at the radiation oncology clinic of the University College Hospital, Ibadan, Nigeria.Methods: A cross-sectional descriptive study was conducted amongst 157 eligible family caregivers of women with advanced breast cancer. The family caregivers completed an interviewer-administered questionnaire, which included the socio-demographic data, the caregiving process and the Zarit Burden Interview (ZBI). Logistic regression was used to identify factors, and ethical approval was obtained.Results: Over half (53%) of the respondents were males with spousal caregivers dominantly constituting 27.4% of all respondents, closely followed by daughters (25.5%) of the care recipients. The mean ZBI score was 29.84 ± 13.9. Most (72%) of the caregivers experienced burden. Factors associated with caregiver burden were previous hospitalisation of the care recipient (odds ratio [OR] = 3.74, confidence interval [CI]: 1.67 to 8.38) and perceived dysfunction in patients activities of daily living (OR = 2.57, CI: 1.14 to 5.78).Conclusion: Family caregivers of women with advanced breast cancer experience burden of care. Recognition of this vulnerable population and the care recipient as a dyad is a sine qua non in mitigating the burden associated with their caregiving role.


2001 ◽  
Vol 28 (2D) ◽  
pp. 15-17
Author(s):  
PierFranco Conte ◽  
Barbara Salvadori ◽  
Sara Donati ◽  
Elisabetta Landucci ◽  
Alessandra Gennari

2001 ◽  
Vol 28 (4) ◽  
pp. 344-358 ◽  
Author(s):  
Harold J. Burstein ◽  
Craig A. Bunnell ◽  
Eric P. Winer

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