The hospice industry is expanding dramatically. The number of hospices has more than doubled from 1,600 in 1990 to over 3,600 in 2004. Despite this dramatic growth in hospice and increasing evidence of its benefits to patients with serious illness and their families, only 20% of older adults who die each year elect to receive hospice services. The availability of hospice nationally is an unstudied, yet potentially key factor in understanding hospice use. Studying the distribution of hospices nationally is also important for identifying the types of communities, in terms of racial and ethnic composition, income profile, degree of rurality and other factors, where gaps in the availability of hospice exist. A second critical aspect of understanding access to hospice is the types of services provided to patients and families that do access hospice. Recent evidence suggests that there is substantial variation across hospices in the care provided to patients and families; however, detailed assessments of such variability and the key processes of care used to deliver hospice services are lacking. Such information is instrumental to improving the quality of hospice care across the country. To address these issues, I will examine the availability of hospice nationally by estimating the percentage of older individuals in the U.S. that live too far from a hospice agency to have reasonable access to hospice services. I will use a novel technique involving the calculation of driving times between population centers and the nearest hospice agency to estimate the percentage of older individuals without reasonable access to hospice, and how this has changed over time. I will determine how availability of hospice varies by key characteristics of communities including demographic and socioeconomic factors. Last, I will conduct a qualitative study to develop a taxonomy of key processes of care used to deliver hospice services and generate hypotheses about potential predictors of variation in these key processes of care to be tested in a future study. Relevance to public health: This research will determine the percentage of older adults that live too far from a hospice agency to have reasonable access to hospice services. It will identify how availability hospice varies across communities that differ in terms of racial and ethnic composition, income, and degree of rurality. This information is critical for understanding disparities in use of hospice and for informing policies to increase the availability of hospice to patients with terminal illness and their families. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Nursing Research (NINR)
Type
Career Transition Award (K99)
Project #
1K99NR010495-01
Application #
7248490
Study Section
National Institute on Aging Initial Review Group (NIA)
Program Officer
Boyington, Josephine
Project Start
2007-09-01
Project End
2009-07-31
Budget Start
2007-09-01
Budget End
2008-07-31
Support Year
1
Fiscal Year
2007
Total Cost
$89,911
Indirect Cost
Name
Mount Sinai School of Medicine
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
078861598
City
New York
State
NY
Country
United States
Zip Code
10029
Aldridge, Melissa D; Schlesinger, Mark; Barry, Colleen L et al. (2014) National hospice survey results: for-profit status, community engagement, and service. JAMA Intern Med 174:500-6
Canavan, Maureen E; Aldridge Carlson, Melissa D; Sipsma, Heather L et al. (2013) Hospice for nursing home residents: does ownership type matter? J Palliat Med 16:1221-6
Aldridge Carlson, Melissa D (2013) Research methods priorities in geriatric palliative medicine. J Palliat Med 16:838-42
Aldridge Carlson, Melissa D; Barry, Colleen L; Cherlin, Emily J et al. (2012) Hospices' enrollment policies may contribute to underuse of hospice care in the United States. Health Aff (Millwood) 31:2690-8
Barry, Colleen L; Carlson, Melissa D A; Thompson, Jennifer W et al. (2012) Caring for grieving family members: results from a national hospice survey. Med Care 50:578-84
Carlson, Melissa D A; Barry, Colleen; Schlesinger, Mark et al. (2011) Quality of palliative care at US hospices: results of a national survey. Med Care 49:803-9
Legler, Aron; Bradley, Elizabeth H; Carlson, Melissa D A (2011) The effect of comorbidity burden on health care utilization for patients with cancer using hospice. J Palliat Med 14:751-6
Carlson, Melissa D A; Lim, Betty; Meier, Diane E (2011) Strategies and innovative models for delivering palliative care in nursing homes. J Am Med Dir Assoc 12:91-8
Carlson, Melissa D A; Herrin, Jeph; Du, Qingling et al. (2010) Impact of hospice disenrollment on health care use and medicare expenditures for patients with cancer. J Clin Oncol 28:4371-5
Goldstein, Nathan; Carlson, Melissa; Livote, Elayne et al. (2010) Brief communication: Management of implantable cardioverter-defibrillators in hospice: A nationwide survey. Ann Intern Med 152:296-9

Showing the most recent 10 out of 14 publications