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January 1, 2018Journal of Health Care for the Poor and UnderservedOpen Access

Social and Behavioral Factors in Sickle Cell Disease: Employment Predicts Decreased Health Care Utilization

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Authors

HWHants WilliamsStony Brook UniversityRSRN Susan SilvaGeorgia Department of Natural ResourcesDCDavid ClineAtrium Health Wake Forest Baptist

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Cite This Study

Williams et al. (2018) studied this question.

synapsesocial.com/papers/6a62753df5a6cede3a89ece0https://doi.org/10.1353/hpu.2018.0060
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Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1The psychosocial experience of people with sickle cell disease and its impact on quality of life: Qualitative findings from focus groups2002 · 127 citations
  2. 2Use and satisfaction with the Healthcare System of the chronic pain patients in Spain: results from a nationwide study2016 · 18 citations
  3. 3Discord of Biological and Psychological Measures in a Group of Depressed African American and White Cancer Patients2011 · 3 citations
  4. 4A systematic review of the association between depression and health care utilization in children and adults with sickle cell disease2016 · 123 citations