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A Needs Assessment of Persons With Sickle Cell Disease in a Major Medical Center in North Carolina.

Publication ,  Journal Article
Masese, RV; Crego, N; Douglas, C; Rains, G; Bonnabeau, E; DeMartino, T; Shah, N; Tanabe, P
Published in: N C Med J
2021

BACKGROUND Sickle cell disease (SCD) is a complex disease associated with many complications and a shortened lifespan. In 2016, the National Heart, Lung and Blood Institute funded 8 centers in the United States to form the Sickle Cell Disease Implementation Consortium, with the goal of improving SCD care. The aim of our study was to describe SCD self-efficacy, pain interference, and barriers to care from the perspective of persons with SCD in the North Carolina center.METHODS Persons with SCD, aged 15 and older were recruited from a large SCD center in North Carolina. Surveys, focus groups, and interviews were completed.RESULTS Fifty-one people completed a survey, and 14 people completed an interview or focus group. Barriers identified in the survey included self-care barriers, misconceptions related to hydroxyurea (an oral medication that reduces rates of pain crisis), limited provider knowledge, and stigma. Concerning self-efficacy, participants reported that they were able to manage their pain symptoms most of the time. Pain interfered most with the ability to participate in social and day-to-day activities.Common themes from the focus groups and interviews included misconceptions about hydroxyurea, pain, provider knowledge, stigma, co-management, transportation, and insurance. Recommendations to improve care included the use of case managers, utilization of treatment guidelines, individualized pain protocols, and effective co-management by providers.LIMITATIONS Participants were recruited from 1 SCD center and may not be representative of the entire SCD population in North Carolina.CONCLUSIONS Participants described many perceived barriers to care, and their responses suggest a need for improvements in patient hydroxyurea education, provider knowledge, and care coordination.

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Published In

N C Med J

DOI

ISSN

0029-2559

Publication Date

2021

Volume

82

Issue

5

Start / End Page

312 / 320

Location

United States

Related Subject Headings

  • United States
  • Pain
  • North Carolina
  • Needs Assessment
  • Hydroxyurea
  • Humans
  • Anemia, Sickle Cell
  • 42 Health sciences
  • 32 Biomedical and clinical sciences
  • 11 Medical and Health Sciences
 

Citation

APA
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Masese, R. V., Crego, N., Douglas, C., Rains, G., Bonnabeau, E., DeMartino, T., … Tanabe, P. (2021). A Needs Assessment of Persons With Sickle Cell Disease in a Major Medical Center in North Carolina. N C Med J, 82(5), 312–320. https://doi.org/10.18043/ncm.82.5.312
Masese, Rita V., Nancy Crego, Christian Douglas, Gary Rains, Emily Bonnabeau, Terri DeMartino, Nirmish Shah, and Paula Tanabe. “A Needs Assessment of Persons With Sickle Cell Disease in a Major Medical Center in North Carolina.N C Med J 82, no. 5 (2021): 312–20. https://doi.org/10.18043/ncm.82.5.312.
Masese RV, Crego N, Douglas C, Rains G, Bonnabeau E, DeMartino T, et al. A Needs Assessment of Persons With Sickle Cell Disease in a Major Medical Center in North Carolina. N C Med J. 2021;82(5):312–20.
Masese, Rita V., et al. “A Needs Assessment of Persons With Sickle Cell Disease in a Major Medical Center in North Carolina.N C Med J, vol. 82, no. 5, 2021, pp. 312–20. Pubmed, doi:10.18043/ncm.82.5.312.
Masese RV, Crego N, Douglas C, Rains G, Bonnabeau E, DeMartino T, Shah N, Tanabe P. A Needs Assessment of Persons With Sickle Cell Disease in a Major Medical Center in North Carolina. N C Med J. 2021;82(5):312–320.

Published In

N C Med J

DOI

ISSN

0029-2559

Publication Date

2021

Volume

82

Issue

5

Start / End Page

312 / 320

Location

United States

Related Subject Headings

  • United States
  • Pain
  • North Carolina
  • Needs Assessment
  • Hydroxyurea
  • Humans
  • Anemia, Sickle Cell
  • 42 Health sciences
  • 32 Biomedical and clinical sciences
  • 11 Medical and Health Sciences