Literature DB >> 31038384

Awareness of Palliative Care among a Nationally Representative Sample of U.S. Adults.

Neha Trivedi1, Emily B Peterson1, Erin M Ellis1, Rebecca A Ferrer1, Erin E Kent1, Wen-Ying Sylvia Chou1.   

Abstract

Background: Palliative care can alleviate symptom burden, reduce psychosocial distress, and improve quality of life for patients suffering from serious or life-threatening illnesses. However, the extent to which U.S. adults are aware of or understand the goals and benefits of palliative care is not well understood. Public awareness of palliative care is necessary to change norms and create demand, and as such, limited awareness may be a significant barrier to palliative care uptake. An assessment of current palliative care awareness in the United States is needed to inform the health care sector's improving palliative care communication and delivery. Objective: To examine the prevalence of palliative care awareness among a nationally-representative sample of U.S. adults and to identify sociodemographic and health-related characteristics associated with palliative care awareness. Design: Weighted data from the Health Information National Trends Survey (HINTS 5, Cycle 2 [2018], N = 3445) were used to produce frequencies of the characteristics, and associations with palliative care awareness were determined through multiple logistic regression.
Results: An estimated 71% of U.S. adults reported having never heard of palliative care. Older individuals, those with higher educational attainment, women, and whites (vs. nonwhites) had greater odds of palliative care awareness. Conclusions: These data suggest there is limited awareness of palliative care in the United States, despite its documented benefits. Addressing this awareness gap is a priority to change norms around using palliative care services. Community- and population-based interventions are necessary to raise awareness and inform the public about palliative care.

Entities:  

Keywords:  end of life; palliative care; quality of life

Mesh:

Year:  2019        PMID: 31038384      PMCID: PMC6998043          DOI: 10.1089/jpm.2018.0656

Source DB:  PubMed          Journal:  J Palliat Med        ISSN: 1557-7740            Impact factor:   2.947


  13 in total

1.  Palliative and end-of-life care in the African American community.

Authors:  L Crawley; R Payne; J Bolden; T Payne; P Washington; S Williams
Journal:  JAMA       Date:  2000-11-15       Impact factor: 56.272

2.  Practice-Based Research Priorities for Palliative Care: Results From a Research-to-Practice Consensus Workshop.

Authors:  Karl Pillemer; Emily K Chen; Catherine Riffin; Holly Prigerson; M C Reid
Journal:  Am J Public Health       Date:  2015-09-17       Impact factor: 9.308

3.  A matter of definition--key elements identified in a discourse analysis of definitions of palliative care.

Authors:  T Pastrana; S Jünger; C Ostgathe; F Elsner; L Radbruch
Journal:  Palliat Med       Date:  2008-04       Impact factor: 4.762

Review 4.  Association Between Palliative Care and Patient and Caregiver Outcomes: A Systematic Review and Meta-analysis.

Authors:  Dio Kavalieratos; Jennifer Corbelli; Di Zhang; J Nicholas Dionne-Odom; Natalie C Ernecoff; Janel Hanmer; Zachariah P Hoydich; Dara Z Ikejiani; Michele Klein-Fedyshin; Camilla Zimmermann; Sally C Morton; Robert M Arnold; Lucas Heller; Yael Schenker
Journal:  JAMA       Date:  2016-11-22       Impact factor: 56.272

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Authors:  Betty R Ferrell; Jennifer S Temel; Sarah Temin; Thomas J Smith
Journal:  J Oncol Pract       Date:  2016-11-01       Impact factor: 3.840

6.  The Health Information National Trends Survey (HINTS): development, design, and dissemination.

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7.  A new international framework for palliative care.

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Journal:  Eur J Cancer       Date:  2004-10       Impact factor: 9.162

Review 8.  Advance Care Planning in palliative care: a systematic literature review of the contextual factors influencing its uptake 2008-2012.

Authors:  Allison Lovell; Patsy Yates
Journal:  Palliat Med       Date:  2014-05-12       Impact factor: 4.762

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Authors:  Jonathan Koffman; Geraldine Burke; Angela Dias; Bharti Raval; Judi Byrne; Juan Gonzales; Charles Daniels
Journal:  Palliat Med       Date:  2007-03       Impact factor: 4.762

10.  Threading the cloak: palliative care education for care providers of adolescents and young adults with cancer.

Authors:  Lori Wiener; Meaghann Shaw Weaver; Cynthia J Bell; Ursula M Sansom-Daly
Journal:  Clin Oncol Adolesc Young Adults       Date:  2015-01-09
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  7 in total

1.  "I'd Have to Basically Be on My Deathbed": Heart Failure Patients' Perceptions of and Preferences for Palliative Care.

Authors:  Rachel A Hadler; Brett R Curtis; Dara Z Ikejiani; David B Bekelman; Matthew Harinstein; Marie A Bakitas; Rachel Hess; Robert M Arnold; Dio Kavalieratos
Journal:  J Palliat Med       Date:  2020-01-09       Impact factor: 2.947

2.  Racial and ethnic disparities in palliative care utilization among gynecological cancer patients.

Authors:  Jessica Y Islam; April Deveaux; Rebecca A Previs; Tomi Akinyemiju
Journal:  Gynecol Oncol       Date:  2020-12-02       Impact factor: 5.482

3.  Palliative Care Communication: Outcomes From COMFORT, a Train-the-Trainer Course for Providers.

Authors:  Elaine Wittenberg; Joy Goldsmith; Betty Ferrell; Haley Buller; Yesenia Mendoza; Sandra L Ragan
Journal:  Clin J Oncol Nurs       Date:  2020-02-01       Impact factor: 1.027

4.  Predictors of Palliative Care Knowledge: Findings from the Health Information National Trends Survey.

Authors:  Motolani E Ogunsanya; Elizabeth A Goetzinger; Oluwatomi F Owopetu; Paulette D Chandler; Lauren E O'Connor
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2021-06-04       Impact factor: 4.090

5.  Knowledge of and beliefs about palliative care in a nationally-representative U.S. sample.

Authors:  Jennifer M Taber; Erin M Ellis; Maija Reblin; Lee Ellington; Rebecca A Ferrer
Journal:  PLoS One       Date:  2019-08-15       Impact factor: 3.240

6.  Characterizing uncertainty in goals-of-care discussions among black and white patients: a qualitative study.

Authors:  Annie T Chen; Shelley Tsui; Rashmi K Sharma
Journal:  BMC Palliat Care       Date:  2022-02-17       Impact factor: 3.234

7.  Where would Canadians prefer to die? Variation by situational severity, support for family obligations, and age in a national study.

Authors:  Laura M Funk; Corey S Mackenzie; Maria Cherba; Nicole Del Rosario; Marian Krawczyk; Andrea Rounce; Kelli Stajduhar; S Robin Cohen
Journal:  BMC Palliat Care       Date:  2022-08-01       Impact factor: 3.113

  7 in total

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