Burden in caregivers of older adults with advanced illness
- PMID: 21087225
- PMCID: PMC3058825
- DOI: 10.1111/j.1532-5415.2010.03177.x
Burden in caregivers of older adults with advanced illness
Abstract
Objectives: To examine caregiver burden over time in caregivers of patients with advanced chronic disease.
Design: Observational cohort with interviews over 12 months.
Setting: Community.
Participants: Caregivers of 179 community-living persons aged 60 and older with advanced cancer, heart failure (HF), or chronic obstructive pulmonary disease (COPD).
Measurements: Caregiver burden was assessed using a short-form of the Zarit Burden Inventory to measure psychosocial distress.
Results: At baseline, the median caregiver burden was 5 (interquartile range (IQR) 1-11), which indicates that the caregiver endorsed having at least two of 10 distressing concerns at least some of the time. Only 10% reported no burden. Although scores increased modestly over time, the association between time and burden was not significant in longitudinal multivariable analysis. High burden was associated with caregiver need for more help with daily tasks (odds ratio (OR)=23.13, 95% confidence interval (CI)=5.94-90.06) and desire for greater communication with the patient (OR=2.53, 95% CI=1.16-5.53). The longitudinal multivariable analysis did not yield evidence of associations between burden and patient sociodemographic or health characteristics.
Conclusion: Caregiver burden was common in caregivers of patients with cancer, HF, and COPD. High burden was associated with the caregiver's report of need for greater help with daily tasks but not with objective measures of the patient's need for assistance, such as symptoms or functional status, suggesting that burden may be a measure of the caregiver's ability to adapt to the caregiving role.
© 2010, Copyright the Authors. Journal compilation © 2010, The American Geriatrics Society.
Conflict of interest statement
Figures
Comment in
-
Research on family caregivers: understanding levels of burden and how to provide assistance.Home Healthc Nurse. 2013 Jun;31(6):331-7. doi: 10.1097/NHH.0b013e3182932f84. Home Healthc Nurse. 2013. PMID: 23736166
References
-
- Rabow MW, Hauser JM, Adams J. Supporting family caregivers at the end of life: “they don’t know what they don’t know”. JAMA. 2004;291:483–491. - PubMed
-
- Zarit SH, Reever KE, Bach-Peterson J. Relatives of the impaired elderly: Correlates of feelings of burden. Gerontologist. 1980;20:649–655. - PubMed
-
- Covinsky KE, Goldman L, Cook EF, et al. The impact of serious illness on patients’ families. SUPPORT investigators study to understand prognoses and preferences for outcomes and risks of treatment. JAMA. 1994;272:1839–1844. - PubMed
-
- Emanuel EJ, Fairclough DL, Slutsman J, et al. Understanding economic and other burdens of terminal illness: The experience of patients and their caregivers. Ann Intern Med. 2000;132:451–459. - PubMed
-
- Beery LC, Prigerson HG, Bierhals AJ, et al. Traumatic grief, depression and caregiving in elderly spouses of the terminally ill. Omega: Int Manage Sci. 1997;35:261–279.
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Research Materials
Miscellaneous
