Palliative care experiences among adults from underrepresented racial and ethnic groups in the United States : a scoping review

Article indépendant

ODURO, Elisha Baafi | JACKSON, Amy | FU, Yunting | CARPENTER, Joan G.

BACKGROUND: Patients from underrepresented racial and ethnic groups (URGs) in the United States (US) experience disparities in accessing palliative care (PC) at the end of life (EOL). Additionally, little effort has been made to understand their experiences with PC. OBJECTIVES: To identify and synthesize existing literature on PC experiences among adults from URGs in nursing homes, community settings, and hospitals in the US. METHODS: Guided by the Joanna Briggs Institute methodological recommendation and Preferred Reporting Items for Systematic Reviews and Meta-Analyses Extension for Scoping Reviews, we conducted a scoping review. We searched PubMed, EMBASE, CINAHL, Scopus, and ProQuest Dissertations & Theses Global from inception to January 2024. RESULTS: We included five studies representing Hispanic/Latino, American Indian, African/Black American, and Chinese individuals. Data were organized around two themes: navigating PC pathway and choices and practices during PC. Navigating PC pathway theme highlights that despite the several barriers URGs face when accessing PC, they seek PC services due to their limited formal family assistance in managing their chronic conditions and pain. The choices and practices during PC theme emphasize the roles URG family members play in EOL care, the patient's care preferences, and their spiritual practices and beliefs related to EOL care. CONCLUSION: This scoping review reveals limited literature about URG experiences with PC and highlights the need for more studies to focus on making PC services more accessible to URGs and providing culturally sensitive care to meet the needs of the diverse growing US population.

http://dx.doi.org/10.1177/10499091241273403

Voir la revue «The American journal of hospice and palliative care»

Autres numéros de la revue «The American journal of hospice and palliative care»

Consulter en ligne

Suggestions

Du même auteur

Telehealth palliative care in nursing homes :...

Article indépendant | WALTON, Lyle | Journal of the American Medical Directors Association | n°3 | vol.24

Objectives: Many adults older than 65 spend time in a nursing home (NH) at the end of life where specialist palliative care is limited. However, telehealth may improve access to palliative care services. A review of the literature...

Telehealth palliative care in nursing homes :...

Article indépendant | WALTON, Lyle | Journal of the American Medical Directors Association | n°3 | vol.24

Objectives: Many adults older than 65 spend time in a nursing home (NH) at the end of life where specialist palliative care is limited. However, telehealth may improve access to palliative care services. A review of the literature...

Palliative care in nursing homes : a qualitat...

Article indépendant | COLE, Connie S. | Journal of the American Geriatrics Society

Palliative care (PC) is vital for nursing home (NH) residents to ensure that people living with serious illness receive the best possible quality of life and care. Despite high symptom burden reported by most NH residents, their f...

De la même série

Life story themes : a qualitative analysis of...

Article indépendant | SKINNER, Shannon | The American journal of hospice and palliative care | n°9 | vol.366

OBJECTIVE: To identify common themes and topics that patients nearing the end of life want to discuss when sharing their life stories. METHODS: Twenty audio-recorded transcripts of open-ended interviews of patients cared for by a ...

Students' experiences with death and dying pr...

Article indépendant | TALWALKAR, Jaideep S. | The American journal of hospice and palliative care | n°11 | vol.366

BACKGROUND: Personal experiences with death and dying are common among medical students, but little is known about student attitudes and emotional responses to these experiences. Our objectives were to ascertain matriculating medi...

Managing end of life care for the critically ...

Article indépendant | BASS, Kathryn | The American journal of hospice and palliative care | n°1 | vol.42

Background: Navigating medical care at the end of life can be a challenging experience for patients. There are also significant resource burdens, including intensive care unit (ICU) admissions, accompanying terminal illness. For a...

End-of-life care for patients with end-stage ...

Article indépendant | RIVERA, Frederick Berro | The American journal of hospice and palliative care | n°1 | vol.41

Heart failure (HF) is a chronic, debilitating condition associated with significant morbidity, mortality, and socioeconomic burden. Patients with end-stage HF (ESHF) who are not a candidate for advanced therapies will continue to ...

Hospice patients' end-of-life dreams and visi...

Article indépendant | RABITTI, Elisa | The American journal of hospice and palliative care | n°1 | vol.41

When conscious, about 50% to 60% of hospice patients report a "visitation" by someone who is not there while they dream or are awake: a phenomenon known as End-of-Life Dreams and Visions (ELDVs). Since the dying process is frequen...

Chargement des enrichissements...