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| Home / College Guide / Exploring distress experiences of patients with sickle cell disease |
| Posted on Tuesday, July 09 @ 00:00:10 PDT |
While distress is well-documented in patients with sickle cell disease, sources of distress and how patients manage distress have not been well explored. A new study
appearing in Qualitative Research in Health seeks to change this.
“Our study found that the most profound source of distress for patients with sickle cell disease in a home visit program was anticipating and going to acute care centers to manage their acute pain,” said senior study author Maryanna Klatt, Ph.D., director of the Center for Integrative Health at The Ohio State University Wexner Medical Center.
These findings bolster researchers’
earlier perspective published in the New England Journal of Medicine that cited a need for a biopsychosocial model to treat chronic pain in sickle cell disease.
Researchers recruited 11 patients with sickle cell from a home visit program at Ohio State Wexner Medical Center between February and July 2021. They wanted to identify sources of distress for persons with sickle cell.
A researcher conducted one-on-one semi-structured interviews with study participants. The research team coded and analyzed all interview transcripts.
Participants said the most profound source of distress was clinical encounters in the emergency department and intermediate care center to manage acute pain flares.
“We found that there is often a performative element for persons with sickle cell in emergency and intermediate care center settings. They feel they have to present in a certain way for providers to see their pain as credible and treat it promptly. Yet often, patients are simply incapable of performing their pain, or ‘crying on cue,’ as one participant put it,” said study first author Janet Childerhose, Ph.D., a research assistant professor in the Department of Internal Medicine at the Ohio State University’s College of Medicine.
“Our analysis also found stigma and racism surround the care of this neglected disease. Participants lack any sense of control over their pain management plan,” said Klatt, who is also a professor in the Department of Family and Community Medicine. “Researchers may wish to consider how these settings could better address patient distress, and providers may wish to adopt participant recommendations to reduce distress associated with seeking pain treatment in acute care settings.”
More information:
Janet E. Childerhose et al, “I can’t cry on cue”: Exploring distress experiences of persons with sickle cell, SSM – Qualitative Research in Health (2024).
DOI: 10.1016/j.ssmqr.2024.100426
Citation:
Exploring distress experiences of patients with sickle cell disease (2024, July 8)
exploring-distress-patients-sickle-cell.html
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. The content is provided for information purposes only.
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