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Caregiver Burden, Quality of Life and Related Factors in Family Caregivers of Dementia Patients in Turkey

Date
2020
Author
Baykal, Dilek
Hanagasi, Hasmet
Erturk, Sumeyye
Tulek, Zeliha
Gurvit, İbrahim Hakan
Bilgic, Başar
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Abstract
© 2020 Taylor & Francis Group, LLC.This study aimed to evaluate caregiver burden and quality of life (QoL) and their predictors in family caregivers of dementia patients. A descriptive cross-sectional survey was carried out with a sample of 102 patients and their family caregivers. The Caregiver Burden Inventory (CBI) and Short Form-12 (SF-12) were used to collect data. CBI mean score was 37.97 ± 21.30. Mean scores of SF-12 sub-domains varied between 36.02 and 77.94 and were significantly lower as compared to normative means of the general population, excluding only the physical health subdomain. Among several patient and caregiver-related correlations, the number of medications and worse cognitive function of the patient, caregiver’s age and having limited space at home were found as predictors of burden, whereas caregiver’s chronic disease and having a limited space were predictors of QoL. Also, the burden and QoL were correlated. This study demonstrated a high burden and low QoL in dementia caregivers. In societies where caregivers are mostly informal such as that in Turkey, supportive systems should be established.
URI
http://hdl.handle.net/20.500.12627/3785
https://doi.org/10.1080/01612840.2019.1705945
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85083569818&origin=inward
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Creative Commons Lisansı

İstanbul Üniversitesi Akademik Arşiv Sistemi (ilgili içerikte aksi belirtilmediği sürece) Creative Commons Alıntı-GayriTicari-Türetilemez 4.0 Uluslararası Lisansı ile lisanslanmıştır.

DSpace software copyright © 2002-2016  DuraSpace
Contact Us | Send Feedback
Theme by 
Atmire NV