TY - JOUR
T1 - Caregivers of older adults with cognitive impairment
AU - DeFries, Erin L.
AU - McGuire, Lisa C.
AU - Andresen, Elena M.
AU - Brumback, Babette A.
AU - Anderson, Lynda A.
N1 - Funding Information:
Funding for this project for authors Andresen and DeFries was from the Centers for Disease Control and Prevention’s (CDC’s) National Center on Birth Defects and Developmental Disabilities via the Association for Prevention Teaching and Research (grant no. PEP-2003-004) and the National Center for Chronic Disease Prevention and Health Promotion (grant no. 200-2006-M-18187). We thank the team at the North Carolina BRFSS for their help in collecting the data used in our analyses and the members of the CDC’s Behavioral Surveillance Branch for their assistance in developing the database. In addition, we thank Bill Garvin for his assistance and expertise in reweighting the data.
PY - 2009
Y1 - 2009
N2 - Introduction: Because of the growing number of caregivers and the awareness of related health and quality-of-life issues, caregiving has emerged as an important public health issue. We examined the characteristics and caregiving experiences of caregivers of people with and without cognitive impairment. Methods: Participants (n = 668) were adults who responded to the 2005 North Carolina Behavioral Risk Factor Surveillance System. Caregivers were people who provided regular care to a family member or friend aged 60 years or older either with or without cognitive impairment (ie, memory loss, confusion, or Alzheimer's disease). Results: Demographic characteristics of caregivers of people with cognitive impairment were similar to those of caregivers of people without cognitive impairment. However, compared with caregivers of people without cognitive impairment, caregivers of people with cognitive impairment reported higher levels of disability, were more likely to be paid, and provided care for a longer duration. Care recipients with cognitive impairment were more likely than care recipients without cognitive impairment to be older, have dementia or confusion, and need assistance with memory and learning. Conclusion: State-level caregiving surveillance is vital in assessing and responding to the needs of the growing number of caregivers.
AB - Introduction: Because of the growing number of caregivers and the awareness of related health and quality-of-life issues, caregiving has emerged as an important public health issue. We examined the characteristics and caregiving experiences of caregivers of people with and without cognitive impairment. Methods: Participants (n = 668) were adults who responded to the 2005 North Carolina Behavioral Risk Factor Surveillance System. Caregivers were people who provided regular care to a family member or friend aged 60 years or older either with or without cognitive impairment (ie, memory loss, confusion, or Alzheimer's disease). Results: Demographic characteristics of caregivers of people with cognitive impairment were similar to those of caregivers of people without cognitive impairment. However, compared with caregivers of people without cognitive impairment, caregivers of people with cognitive impairment reported higher levels of disability, were more likely to be paid, and provided care for a longer duration. Care recipients with cognitive impairment were more likely than care recipients without cognitive impairment to be older, have dementia or confusion, and need assistance with memory and learning. Conclusion: State-level caregiving surveillance is vital in assessing and responding to the needs of the growing number of caregivers.
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M3 - Article
C2 - 19288989
AN - SCOPUS:66449090940
SN - 1545-1151
VL - 6
JO - Preventing chronic disease
JF - Preventing chronic disease
IS - 2
M1 - A46
ER -