Literature DB >> 10073202

Does race influence the provision of care to persons with sickle cell disease? Perceptions of multidisciplinary providers.

J Telfair1, J Myers, S Drezner.   

Abstract

This study examined whether multidisciplinary health care providers (HCPs) perceived race of persons with sickle cell disease (SCD) as an influence in the delivery of health care. A total of 227 multidisciplinary HCPs completed the three-item Influence of Patient Race on Provision of Health Care Services Index (Cronbach's alpha = 0.77). Results suggest that African American HCPs were more likely to perceive race as an influence along all scale items, whereas Caucasian and other race HCPs did not. Female HCPs and those who serve adults were more likely than male HCPs and those who serve children to perceive race as having an influence on the quality of health care. Findings suggest a need for the examination of the health care delivery systems in which persons with SCD receive care to determine if race does, in fact, affect the delivery of health care and to explain the discrepancies in the perceptions of the HCPs.

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Mesh:

Year:  1998        PMID: 10073202     DOI: 10.1353/hpu.2010.0127

Source DB:  PubMed          Journal:  J Health Care Poor Underserved        ISSN: 1049-2089


  6 in total

1.  Perceived discrimination in health care is associated with a greater burden of pain in sickle cell disease.

Authors:  Carlton Haywood; Marie Diener-West; John Strouse; C Patrick Carroll; Shawn Bediako; Sophie Lanzkron; Jennifer Haythornthwaite; Gladys Onojobi; Mary Catherine Beach
Journal:  J Pain Symptom Manage       Date:  2014-04-15       Impact factor: 3.612

2.  Emergency provider analgesic practices and attitudes toward patients with sickle cell disease.

Authors:  Jeffrey A Glassberg; Paula Tanabe; Annie Chow; Katrina Harper; Carlton Haywood; Michael R DeBaun; Lynne D Richardson
Journal:  Ann Emerg Med       Date:  2013-04-03       Impact factor: 5.721

3.  Adult sickle cell quality-of-life measurement information system (ASCQ-Me): conceptual model based on review of the literature and formative research.

Authors:  Marsha J Treadwell; Kathryn Hassell; Roger Levine; San Keller
Journal:  Clin J Pain       Date:  2014-10       Impact factor: 3.442

4.  Emergency Department Provider Survey Regarding Acute Sickle Cell Pain Management.

Authors:  Olufunke Y Martin; Sean M Thompson; Aaron E Carroll; Seethal A Jacob
Journal:  J Pediatr Hematol Oncol       Date:  2020-08       Impact factor: 1.170

5.  Addressing unmet basic needs for children with sickle cell disease in the United States: clinic and staff perspectives.

Authors:  Stephanie Loo; Annelise Brochier; Mikayla Gordon Wexler; Kristin Long; Patricia L Kavanagh; Arvin Garg; Mari-Lynn Drainoni
Journal:  BMC Health Serv Res       Date:  2021-01-12       Impact factor: 2.655

6.  Multiple Levels of Suffering: Discrimination in Health-Care Settings is Associated With Enhanced Laboratory Pain Sensitivity in Sickle Cell Disease.

Authors:  Vani A Mathur; Kasey B Kiley; Carlton Haywood; Shawn M Bediako; Sophie Lanzkron; C Patrick Carroll; Luis F Buenaver; Megan Pejsa; Robert R Edwards; Jennifer A Haythornthwaite; Claudia M Campbell
Journal:  Clin J Pain       Date:  2016-12       Impact factor: 3.442

  6 in total

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