|
|
||||||||
RESEARCH AND PRACTICE |
Maryam Navaie-Waliser and Penny H. Feldman are with the Center for Home Care Policy and Research, Visiting Nurse Service of New York, NY. David A. Gould, Carol Levine, and Alexis N. Kuerbis are with the United Hospital Fund, New York, NY. Karen Donelan is with the Department of Health Policy and Management, Harvard School of Public Health, Boston, Mass.
Correspondence: Requests for reprints should be sent to Maryam Navaie-Waliser, DrPH, Center for Home Care Policy and Research, Visiting Nurse Service of New York, 5 Penn Plaza, 11th Floor, New York, NY 10001 (e-mail: maryam.navaie{at}vnsny.org).
Objectives. This study examined the characteristics, activities, and challenges of high-risk informal caregivers.
Methods. Telephone interviews were conducted with a nationally representative cross-section of 1002 informal caregivers. Vulnerable caregivers with poor health or a serious health condition were compared with nonvulnerable caregivers.
Results. Thirty-six percent of caregivers were vulnerable. Compared with nonvulnerable caregivers, vulnerable caregivers were more likely to have difficulty providing care, to provide higher-intensity care, to report that their physical health had suffered since becoming a caregiver, to be aged 65 years or older, to be married, and to have less than 12 years of education.
Conclusions. Reliance on informal caregivers without considering the caregiver's ability to provide care can create a stressful and potentially unsafe environment for the caregiver and the care recipient.
This article has been cited by other articles:
![]() |
J. N. Wells, C. S. Cagle, P. Bradley, and D. M. Barnes Voices of Mexican American Caregivers for Family Members With Cancer: On Becoming Stronger J Transcult Nurs, July 1, 2008; 19(3): 223 - 233. [Abstract] [PDF] |
||||
![]() |
R. C. Talley and J. E. Crews TALLEY AND CREWS RESPOND Am J Public Health, November 1, 2007; 97(11): 1931 - 1932. [Full Text] [PDF] |
||||
![]() |
M. S. Mittelman, D. L. Roth, O. J. Clay, and W. E. Haley Preserving Health of Alzheimer Caregivers: Impact of a Spouse Caregiver Intervention Am J Geriatr Psychiatry, September 1, 2007; 15(9): 780 - 789. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Pinquart and S. Sorensen Correlates of Physical Health of Informal Caregivers: A Meta-Analysis J. Gerontol. B. Psychol. Sci. Soc. Sci., March 1, 2007; 62(2): P126 - P137. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Hannum Rose, K. F. Bowman, E. E. O'Toole, K. Abbott, T. E. Love, C. Thomas, and N. V. Dawson Caregiver Objective Burden and Assessments of Patient-Centered, Family-Focused Care for Frail Elderly Veterans Gerontologist, February 1, 2007; 47(1): 21 - 33. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Bookman and M. Harrington Family Caregivers: A Shadow Workforce in the Geriatric Health Care System? Journal of Health Politics Policy and Law, January 1, 2007; 32(6): 1005 - 1041. [Abstract] [PDF] |
||||
![]() |
B. Chaix, M. Navaie-Waliser, C. Viboud, I. Parizot, and P. Chauvin Lower utilization of primary, specialty and preventive care services by individuals residing with persons in poor health. Eur J Public Health, April 1, 2006; 16(2): 209 - 216. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. A. Selecky, C. A. H. Eliasson, R. I. Hall, R. F. Schneider, B. Varkey, ACCP Ethics Committee, and D. R. McCaffree Palliative and End-of-Life Care for Patients With Cardiopulmonary Diseases: American College of Chest Physicians Position Statement Chest, November 1, 2005; 128(5): 3599 - 3610. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. O'Mara Who's Taking Care of the Caregiver? J. Clin. Oncol., October 1, 2005; 23(28): 6820 - 6821. [Full Text] [PDF] |
||||
![]() |
L. Fredman, S. Tennstedt, K. A. Smyth, J. D. Kasper, B. Miller, T. Fritsch, M. Watson, and E. L. Harris Pragmatic and Internal Validity Issues in Sampling in Caregiver Studies: A Comparison of Population-Based, Registry-Based, and Ancillary Studies J Aging Health, April 1, 2004; 16(2): 175 - 203. [Abstract] [PDF] |
||||
![]() |
M. W. Rabow, J. M. Hauser, and J. Adams Supporting Family Caregivers at the End of Life: "They Don't Know What They Don't Know" JAMA, January 28, 2004; 291(4): 483 - 491. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. A. Selwyn and M. Forstein Overcoming the False Dichotomy of Curative vs Palliative Care for Late-Stage HIV/AIDS: "Let Me Live the Way I Want to Live, Until I Can't" JAMA, August 13, 2003; 290(6): 806 - 814. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. G. Prigerson, E. Cherlin, J. H. Chen, S. V. Kasl, R. Hurzeler, and E. H. Bradley The Stressful Caregiving Adult Reactions to Experiences of Dying (SCARED) Scale: A Measure for Assessing Caregiver Exposure to Distress in Terminal Care Am J Geriatr Psychiatry, June 1, 2003; 11(3): 309 - 319. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |