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Self‐management recommendations for sickle cell disease: A content analysis of websites

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  • Andrews A. Druye
  • Katherine Nelson
  • Brian Robinson

Abstract

This authors report on the findings of a study designed to establish website‐based self‐management recommendations for sickle cell disease. Google and Yahoo search engines were used to search the World Wide Web. Purposive sampling was used to select 28 websites that met the inclusion criteria. Data were manually collected from health education materials and subjected to qualitative content analysis. Self‐management was conceptualized as actions involving preventive health, self‐monitoring, self‐diagnosing, and self‐treatment. The results show that the websites recommend more self‐management actions for preventive health and self‐treatment than for self‐monitoring and self‐diagnosis. Frequent oral fluid intake, limitation of overactivity, eating a healthy diet, avoiding extreme temperatures, and infections were the most common preventive health recommendations. Daily pain monitoring and general bodily inspections were the most frequent self‐monitoring recommendations. Commonly cited self‐diagnostic indicators were fever, persistent pain, enlarged spleen, and leg ulcers. The use of analgesics and nonpharmacological measures were regularly cited for self‐treatment. Most recommendations were assessed as clinically safe as they align with standards for sickle cell management. Nurses and other professionals should teach clients how to assess the credibility of websites.

Suggested Citation

  • Andrews A. Druye & Katherine Nelson & Brian Robinson, 2020. "Self‐management recommendations for sickle cell disease: A content analysis of websites," Nursing & Health Sciences, John Wiley & Sons, vol. 22(4), pages 881-891, December.
  • Handle: RePEc:wly:nuhsci:v:22:y:2020:i:4:p:881-891
    DOI: 10.1111/nhs.12741
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    References listed on IDEAS

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    1. Coretta M. Jenerette & Cheryl Brewer & Ashley N. Leak, 2011. "Self-Care Recommendations of Middle-Aged and Older Adults with Sickle Cell Disease," Nursing Research and Practice, Hindawi, vol. 2011, pages 1-5, August.
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