Literature DB >> 33423532

Sociodemographic Disparities in Access to Hospice and Palliative Care: An Integrative Review.

Katie E Nelson1, Rebecca Wright1, Anna Peeler1, Teresa Brockie1, Patricia M Davidson1.   

Abstract

BACKGROUND: There is growing evidence of disparities in access to hospice and palliative care services to varying degrees by sociodemographic groups. Underlying factors contributing to access issues have received little systematic attention.
OBJECTIVE: To synthesize current literature on disparities in access to hospice and palliative care, highlight the range of sociodemographic groups affected by these inequities, characterize the domains of access addressed, and outline implications for research, policy, and clinical practice.
DESIGN: An integrative review comprised a systematic search of PubMed, Embase, and CINAHL databases, which was conducted from inception to March 2020 for studies outlining disparities in hospice and palliative care access in the United States. Data were analyzed using critical synthesis within the context of a health care accessibility conceptual framework. Included studies were appraised on methodological quality and quality of reporting.
RESULTS: Of the articles included, 80% employed non-experimental study designs. Study measures varied, but 70% of studies described differences in outcomes by race, ethnicity, or socioeconomic status. Others revealed disparate access based on variables such as age, gender, and geographic location. Overall synthesis highlighted evidence of disparities spanning 5 domains of access: Approachability, Acceptability, Availability, Affordability, and Appropriateness; 60% of studies primarily emphasized Acceptability, Affordability, and Appropriateness.
CONCLUSIONS: This integrative review highlights the need to consider various stakeholder perspectives and attitudes at the individual, provider, and system levels going forward, to target and address access issues spanning all domains.

Entities:  

Keywords:  health services accessibility; healthcare disparities; hospices; palliative care; review

Mesh:

Year:  2021        PMID: 33423532      PMCID: PMC8514114          DOI: 10.1177/1049909120985419

Source DB:  PubMed          Journal:  Am J Hosp Palliat Care        ISSN: 1049-9091            Impact factor:   2.500


  38 in total

1.  Geographic access to hospice in the United States.

Authors:  Melissa D A Carlson; Elizabeth H Bradley; Qingling Du; R Sean Morrison
Journal:  J Palliat Med       Date:  2010-10-27       Impact factor: 2.947

2.  The integrative review: updated methodology.

Authors:  Robin Whittemore; Kathleen Knafl
Journal:  J Adv Nurs       Date:  2005-12       Impact factor: 3.187

Review 3.  Palliative and End-of-Life Care for Lesbian, Gay, Bisexual, and Transgender (LGBT) Cancer Patients and Their Caregivers.

Authors:  Kristin G Cloyes; William Hull; Andra Davis
Journal:  Semin Oncol Nurs       Date:  2018-01-03       Impact factor: 2.315

4.  Statewide Differences in Personality Associated with Geographic Disparities in Access to Palliative Care: Findings on Openness.

Authors:  Michael Hoerger; Laura M Perry; Brittany D Korotkin; Leah E Walsh; Adina S Kazan; James L Rogers; Wasef Atiya; Sonia Malhotra; James I Gerhart
Journal:  J Palliat Med       Date:  2019-01-07       Impact factor: 2.947

5.  Correlates of care for young men with Duchenne and Becker muscular dystrophy.

Authors:  Jennifer G Andrews; Melinda F Davis; F John Meaney
Journal:  Muscle Nerve       Date:  2013-09-11       Impact factor: 3.217

6.  Quality Of End-Of-Life Care Is Higher In The VA Compared To Care Paid For By Traditional Medicare.

Authors:  Risha Gidwani-Marszowski; Jack Needleman; Vincent Mor; Katherine Faricy-Anderson; Derek B Boothroyd; Gary Hsin; Todd H Wagner; Karl A Lorenz; Manali I Patel; Vilija R Joyce; Samantha S Murrell; Kavitha Ramchandran; Steven M Asch
Journal:  Health Aff (Millwood)       Date:  2018-01       Impact factor: 6.301

7.  Methods for overcoming barriers in palliative care for ethnic/racial minorities: a systematic review.

Authors:  Donna P Mayeda; Katherine T Ward
Journal:  Palliat Support Care       Date:  2019-12

8.  Mapping the Mixed Methods-Mixed Research Synthesis Terrain.

Authors:  Margarete Sandelowski; Corrine I Voils; Jennifer Leeman; Jamie L Crandell
Journal:  J Mix Methods Res       Date:  2011-12-28

Review 9.  The growth of palliative care in the United States.

Authors:  Mark T Hughes; Thomas J Smith
Journal:  Annu Rev Public Health       Date:  2014       Impact factor: 21.981

10.  Racial and ethnic differences in end-of-life care in the United States: Evidence from the Health and Retirement Study (HRS).

Authors:  Martina Orlovic; Katharine Smith; Elias Mossialos
Journal:  SSM Popul Health       Date:  2018-11-30
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  11 in total

1.  Anxiety, Depression, Quality of Life, Caregiver Burden, and Perceptions of Caregiver-Centered Communication among Black and White Hospice Family Caregivers.

Authors:  Lauren T Starr; Karen Bullock; Karla Washington; Subhash Aryal; Debra Parker Oliver; George Demiris
Journal:  J Palliat Med       Date:  2021-11-18       Impact factor: 2.947

Review 2.  The Role of Palliative Care in COPD.

Authors:  Anand S Iyer; Donald R Sullivan; Kathleen O Lindell; Lynn F Reinke
Journal:  Chest       Date:  2021-11-03       Impact factor: 10.262

Review 3.  Equity consideration in palliative care policies, programs, and evaluation: an analysis of selected federal and South Australian documents.

Authors:  Sara Javanparast; Julia Anaf; Jennifer Tieman
Journal:  BMC Palliat Care       Date:  2022-06-16       Impact factor: 3.113

4.  Demonstrating LGBTQ+ Affirmative Practice in Groups:: Developing Competence through Simulation-Based Learning.

Authors:  Shelley L Craig; Gio Iacono; Lauren McInroy; Alexa Kirkland; Rachael Pascoe; Toula Kourgiantakis
Journal:  Clin Soc Work J       Date:  2022-08-16

Review 5.  History of Equity, Diversity, and Inclusion in Trauma Surgery: for Our Patients, for Our Profession, and for Ourselves.

Authors:  Esther S Tseng; Brian H Williams; Heena P Santry; Matthew J Martin; Andrew C Bernard; Bellal A Joseph
Journal:  Curr Trauma Rep       Date:  2022-09-05

6.  Addressing inequitable access to hospice care.

Authors:  Catriona R Mayland; Sarah Mitchell; Kate Flemming; Lynn Tatnell; Lesley Roberts; John I MacArtney
Journal:  BMJ Support Palliat Care       Date:  2022-06-16       Impact factor: 4.633

7.  Adding telephone follow-up can improve representativeness of surveys of seriously ill people.

Authors:  Maria DeYoreo; Rebecca Anhang Price; Melissa A Bradley; Danielle Schlang; Cheryl K Montemayor; Anagha Tolpadi; Paul D Cleary; Joan M Teno; Marc N Elliott
Journal:  J Am Geriatr Soc       Date:  2022-02-28       Impact factor: 7.538

8.  Palliative oncology and palliative care.

Authors:  Peter Strang
Journal:  Mol Oncol       Date:  2022-08-12       Impact factor: 7.449

9.  Hospice Enrollment, Future Hospitalization, and Future Costs Among Racially and Ethnically Diverse Patients Who Received Palliative Care Consultation.

Authors:  Lauren T Starr; Connie M Ulrich; G Adriana Perez; Subhash Aryal; Paul Junker; Nina R O'Connor; Salimah H Meghani
Journal:  Am J Hosp Palliat Care       Date:  2021-07-28       Impact factor: 2.090

10.  Assessment of Clinical Palliative Care Trigger Status vs Actual Needs Among Critically Ill Patients and Their Family Members.

Authors:  Christopher E Cox; Deepshikha Charan Ashana; Krista L Haines; David Casarett; Maren K Olsen; Alice Parish; Yasmin Ali O'Keefe; Mashael Al-Hegelan; Robert W Harrison; Colleen Naglee; Jason N Katz; Allie Frear; Elias H Pratt; Jessie Gu; Isaretta L Riley; Shirley Otis-Green; Kimberly S Johnson; Sharron L Docherty
Journal:  JAMA Netw Open       Date:  2022-01-04
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