Hospice quality, race, and disenrollment in hospice enrollees with dementia

Article indépendant

HUNT, Lauren J. | GAN, Siqi | SMITH, Alexander K. | ALDRIDGE, Melissa D. | BOSCARDIN, W. John | HARRISON, Krista L. | JAMES, Jennifer E. | LEE, Alexandra K. | YAFFE, Kristine

Background: Racial and ethnic minoritized people with dementia (PWD) are at high risk of disenrollment from hospice, yet little is known about the relationship between hospice quality and racial disparities in disenrollment among PWD. Objective: To assess the association between race and disenrollment between and within hospice quality categories in PWD. Design/Setting/Subjects: Retrospective cohort study of 100% Medicare beneficiaries 65+ enrolled in hospice with a principal diagnosis of dementia, July 2012-December 2017. Race and ethnicity (White/Black/Hispanic/Asian and Pacific Islander [AAPI]) was assessed with the Research Triangle Institute (RTI) algorithm. Hospice quality was assessed with the publicly-available Consumer Assessment of Healthcare Providers and Systems (CAHPS) survey item on overall hospice rating, including a category for hospices exempt from public reporting (unrated). Results: The sample included 673,102 PWD (mean age 86, 66% female, 85% White, 7.3% Black, 6.3% Hispanic, 1.6% AAPI) enrolled in 4371 hospices nationwide. Likelihood of disenrollment was higher in hospices in the lowest quartile of quality ratings (vs. highest quartile) for both White (adjusted odds ratio [AOR] 1.12 [95% confidence interval 1.06-1.19]) and minoritized PWD (AOR range 1.2-1.3) and was substantially higher in unrated hospices (AOR range 1.8-2.0). Within both low- and high-quality hospices, minoritized PWD were more likely to be disenrolled compared with White PWD (AOR range 1.18-1.45). Conclusions: Hospice quality predicts disenrollment, but does not fully explain disparities in disenrollment for minoritized PWD. Efforts to improve racial equity in hospice should focus both on increasing equity in access to high-quality hospices and improving care for racial minoritized PWD in all hospices.

http://dx.doi.org/10.1089/jpm.2023.0011

Voir la revue «JOURNAL OF PALLIATIVE MEDICINE, 26»

Autres numéros de la revue «JOURNAL OF PALLIATIVE MEDICINE»

Consulter en ligne

Suggestions

Du même auteur

Hospice quality, race, and disenrollment in h...

Article indépendant | HUNT, Lauren J. | JOURNAL OF PALLIATIVE MEDICINE | n°8 | vol.26

Background: Racial and ethnic minoritized people with dementia (PWD) are at high risk of disenrollment from hospice, yet little is known about the relationship between hospice quality and racial disparities in disenrollment among ...

A national study of disenrollment from hospic...

Article indépendant | HUNT, Lauren J. | Journal of the American Geriatrics Society | n°10 | vol.70

Background: People with dementia (PWD) are at high risk for hospice disenrollment, yet little is known about patterns of disenrollment among the growing number of hospice enrollees with dementia. Design: Retrospective, observation...

Hospice use among Medicare beneficiaries with...

Article | BOCK, Meredith | JAMA network open | n°3 | vol.8

IMPORTANCE: Neurodegenerative disorders are now the most common reason that Medicare beneficiaries enroll in hospice for end-of-life care. People with all-cause dementia have high rates of suboptimal hospice use, but little is kno...

De la même série

Feasibility of a palliative care intervention...

Article indépendant | VERMA, Manisha | JOURNAL OF PALLIATIVE MEDICINE | n°3 | vol.36

Background: Patients with hepatocellular cancer (HCC) are at risk for poor quality of life (QoL) and high symptom burden, coupled with limited treatment options. Palliative care (PC) can play an important role in reducing the suff...

"You suffer from being interested" : a tribut...

Article indépendant | MILLER, Pringl | JOURNAL OF PALLIATIVE MEDICINE | n°12 | vol.31

I met Hank during my palliative medicine fellowship after his nurse Cynthia paged me to request a consult for existential suffering. When reviewing Hank's electronic medical record, it became evident he was dying and averse to spe...

Top ten tips palliative care clinicians shoul...

Article indépendant | CHUNG, Jenny E. | JOURNAL OF PALLIATIVE MEDICINE | n°1 | vol.27

As of 2019, there are 4.2 million Filipino Americans (FAs) and 1.9 million Korean Americans (KAs) in the United States, largely concentrated in New York, California, Texas, Illinois, and Washington. In both populations, similar to...

Interventions for family caregivers of patien...

Article indépendant | ALSHAKHS, Sulaiman | JOURNAL OF PALLIATIVE MEDICINE | n°1 | vol.27

There is a need for understanding the breadth of interventions for caregivers of individuals receiving hospice care at home, given the important role caregivers play in caring and the negative outcomes (e.g., depression) associate...

Associations between measures of disability a...

Article indépendant | CHANG, Victoria A. | JOURNAL OF PALLIATIVE MEDICINE | n°1 | vol.27

Background: The modified Rankin Scale (mRS), which measures degree of disability in daily activities, is the most common outcome measure in stroke research. Quality of life (QoL), however, is impacted by factors other than disabil...

Chargement des enrichissements...