Literature DB >> 21425152

Racial disparities in the use of hospice services according to geographic residence and socioeconomic status in an elderly cohort with nonsmall cell lung cancer.

Dale Hardy1, Wenyaw Chan, Chih-Chin Liu, Janice N Cormier, Rui Xia, Eduardo Bruera, Xianglin L Du.   

Abstract

BACKGROUND: The authors investigated whether there were racial disparities in the receipt of hospice services within geographic residence and socioeconomic status (SES) levels.
METHODS: In total, 117,894 patients aged ≥66 years with nonsmall cell lung cancer (NSCLC) were identified from the Surveillance, Epidemiology, and End Results-Medicare linked database who had received hospice services in the last 6 months before death and who died between January 1, 1991 and December 31, 2005. Multivariate odds ratios (ORs) with 95% confidence intervals (CIs) using mixed-effects logistic regression models were used to describe relations.
RESULTS: In urban areas, there were significant disparity trends in age/sex-adjusted rates for blacks and Asians/Pacific Islanders compared with whites (P = .003 and P = .036, respectively). Blacks (OR, 0.79; 95% CI, 0.75-0.82), Asians/Pacific Islanders (OR, 0.42; 95% CI, 0.39-0.46), and Hispanics (OR, 0.81; 95% CI, 0.73-0.91) were less likely to receive hospice services. In rural areas, blacks were 21% less likely to receive hospice services (OR, 0.79; 95% CI, 0.63-0.98). Patients in the poorest socioeconomic status (SES) quartile were 7% less likely to receive hospice services (OR, 0.93; 95% CI, 0.86-1.00). Moreover, within stratified SES quartiles, blacks and Asians/Pacific Islanders had lower receipt of hospice services, and Asians/Pacific Islanders were the least likely to receive hospice services, particularly those in the poorest SES quartile. In general, older patients and women were more likely to receive hospice services.
CONCLUSIONS: There were substantial disparities in the receipt of hospice services among ethnic minorities within urban and rural areas and within SES levels. The results indicated that efforts are needed to identify barriers, enhance support, and educate patients on the benefits of hospice services.
Copyright © 2010 American Cancer Society.

Entities:  

Mesh:

Year:  2010        PMID: 21425152     DOI: 10.1002/cncr.25669

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  28 in total

1.  Dartmouth Atlas: putting end-of-life care on the map but missing psychosocial detail.

Authors:  Holly G Prigerson; Paul K Maciejewski
Journal:  J Support Oncol       Date:  2011-09-23

Review 2.  Cultural and religious considerations in pediatric palliative care.

Authors:  Lori Wiener; Denice Grady McConnell; Lauren Latella; Erica Ludi
Journal:  Palliat Support Care       Date:  2012-05-22

3.  Variation in Intensity and Costs of Care by Payer and Race for Patients Dying of Cancer in Texas: An Analysis of Registry-linked Medicaid, Medicare, and Dually Eligible Claims Data.

Authors:  B Ashleigh Guadagnolo; Kai-Ping Liao; Sharon H Giordano; Linda S Elting; Ya-Chen T Shih
Journal:  Med Care       Date:  2015-07       Impact factor: 2.983

4.  Hospice Use for Infants With Life-Threatening Health Conditions, 2007 to 2010.

Authors:  Lisa C Lindley; Katherine M Newnam
Journal:  J Pediatr Health Care       Date:  2016-05-28       Impact factor: 1.812

5.  Are Trends in Hospitalization Prior to Hospice Use Associated With Hospice Episode Characteristics?

Authors:  Brystana G Kaufman; Carla A Sueta; Cathy Chen; B Gwen Windham; Sally C Stearns
Journal:  Am J Hosp Palliat Care       Date:  2016-07-14       Impact factor: 2.500

6.  Direct Engagement With Communities and Interprofessional Learning to Factor Culture Into End-of-Life Health Care Delivery.

Authors:  Nathan A Boucher
Journal:  Am J Public Health       Date:  2016-03-17       Impact factor: 9.308

7.  Barriers to end-of-life care for African Americans from the providers' perspective: opportunity for intervention development.

Authors:  Ramona L Rhodes; Kim Batchelor; Simon C Lee; Ethan A Halm
Journal:  Am J Hosp Palliat Care       Date:  2013-10-04       Impact factor: 2.500

8.  Geographic variation in black-white differences in end-of-life care for patients with ESRD.

Authors:  Bernadette A Thomas; Rudolph A Rodriguez; Edward J Boyko; Cassianne Robinson-Cohen; Annette L Fitzpatrick; Ann M O'Hare
Journal:  Clin J Am Soc Nephrol       Date:  2013-04-11       Impact factor: 8.237

Review 9.  Social Inequalities in Palliative Care for Cancer Patients in the United States: A Structured Review.

Authors:  Ronit Elk; Tisha M Felder; Ebru Cayir; Cleo A Samuel
Journal:  Semin Oncol Nurs       Date:  2018-08-23       Impact factor: 2.315

10.  Perceptions of the Pediatric Hospice Experience among English- and Spanish-Speaking Families.

Authors:  Rachel Thienprayoon; Emily Marks; Maria Funes; Louizza Maria Martinez-Puente; Naomi Winick; Simon Craddock Lee
Journal:  J Palliat Med       Date:  2015-11-30       Impact factor: 2.947

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