The caregiver burden in lupus: findings from UNVEIL, a national online lupus survey in the United States

被引:20
作者
Al Sawah, S. [1 ]
Daly, R. P. [2 ]
Foster, S. A. [1 ]
Naegeli, A. N. [1 ]
Benjamin, K. [3 ]
Doll, H. [4 ]
Bond, G. [3 ]
Moshkovich, O. [3 ]
Alarcon, G. S. [5 ]
机构
[1] Eli Lilly & Co, Indianapolis, IN 46285 USA
[2] Lupus Fdn Amer Inc, Washington, DC USA
[3] ICON COA, Gaithersburg, MD USA
[4] ICON COA, Oxford, England
[5] Univ Alabama Birmingham, Birmingham, AL USA
关键词
Systemic lupus erythematosus; caregivers; burden; health related quality of life; work productivity; QUALITY-OF-LIFE; ERYTHEMATOSUS; HEALTH; POPULATION; PREVALENCE; INVENTORY; SUPPORT;
D O I
10.1177/0961203316651743
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: Lupus imposes a substantial burden on patients; however, little is known about its impact on those caring for patients with the disease. In this study, we examined the impact caring for patients with lupus' has on caregivers from their own perspective. Methods: UNVEIL was a one-time online national cross-sectional survey developed in partnership with the Lupus Foundation of America and fielded targeting the US Lupus Foundation of America constituents in 2014. Eligible caregivers were adults who self-identified as unpaid caregivers of patients with lupus. Eligible caregivers had to complete a series of sociodemographic questions as well as a series of well established outcome measures, such as the Short Form 12v2 Health Survey, the Work Productivity and Activity Index, the Caregiver Burden Inventory, and the Perceived Benefits of Caregiving Scale. Results: A total of 253 caregivers completed the survey. The majority of caregivers (90.1%) were aged 60 years or younger, more than half (54.2%) were men, and more than half (59.7%) identified themselves as either a spouse or a partner to the patient with lupus they were caring for. Overall health-related quality of life was close to the norm mean of the general US population. Caregivers who were employed missed an average of 12.8% of paid work time due to caregiving responsibilities and reported a 33.5% reduction in on-the-job effectiveness. Nearly half of the caregivers surveyed (49.4%) indicated that their caregiving responsibilities impacted their ability to socialize with friends, and almost all caregivers (97.6%) reported experiencing increased anxiety and stress in relation to their caregiving role. Conclusions: Caregiving for patients with lupus has a substantial impact on the work productivity and the social and emotional functioning of caregivers. Healthcare professionals and policymakers should continually assess the impact of healthcare decisions on the well-being of those caring for patients with lupus.
引用
收藏
页码:54 / 61
页数:8
相关论文
共 24 条
[1]  
[Anonymous], 2002, USERS MANUAL SF 12V2
[2]  
[Anonymous], 2015, Caregiving in the U.S. 2015
[3]  
[Anonymous], 2015, OPTUM SF 12V2 HLTH S
[4]  
[Anonymous], 2015, PERCEIVED BENEFIT CA
[5]  
[Anonymous], 2015, CAREGIVER BURDEN INV
[6]   Negative and positive health effects of casing for a disabled spouse: Longitudinal findings from the caregiver health effects study [J].
Beach, SR ;
Schulz, R ;
Yee, JL ;
Jackson, S .
PSYCHOLOGY AND AGING, 2000, 15 (02) :259-271
[7]   Group living homes for older people with dementia: The effects on psychological distress of informal caregivers [J].
Boekhorst, Selma te ;
Pot, Anne Margriet ;
Depla, Marja ;
Smit, Dieneke ;
de lange, Jacomine ;
Eefsting, Jan .
AGING & MENTAL HEALTH, 2008, 12 (06) :761-768
[8]   Perceptions of economic hardship and emotional health in a pilot sample of family caregivers [J].
Bradley, Sarah E. ;
Sherwood, Paula R. ;
Kuo, Jean ;
Kammerer, Candace M. ;
Gettig, Elizabeth A. ;
Ren, Dianxu ;
Rohrer, Wesley M. ;
Donovan, Heidi S. ;
Hricik, Allison ;
Newberry, Alyssa ;
Given, Barbara .
JOURNAL OF NEURO-ONCOLOGY, 2009, 93 (03) :333-342
[9]   Exploring the caregiver burden inventory (CBI): Further evidence for a multidimensional view of burden [J].
Caserta, MS ;
Lund, DA ;
Wright, SD .
INTERNATIONAL JOURNAL OF AGING & HUMAN DEVELOPMENT, 1996, 43 (01) :21-34
[10]   Epidemiology and sociodemographics of systemic lupus erythematosus and lupus nephritis among US adults with Medicaid coverage, 20002004 [J].
Feldman, Candace H. ;
Hiraki, Linda T. ;
Liu, Jun ;
Fischer, Michael A. ;
Solomon, Daniel H. ;
Alarcon, Graciela S. ;
Winkelmayer, Wolfgang C. ;
Costenbader, Karen H. .
ARTHRITIS AND RHEUMATISM, 2013, 65 (03) :753-763