Needs of Individuals Living With Hepatitis Delta Virus and Their Caregivers, 2016–2019
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Needs of Individuals Living With Hepatitis Delta Virus and Their Caregivers, 2016–2019
  • Published Date:

    December 17 2020

  • Source:
    Prev Chronic Dis. 2020; 17
  • Language:
    English
Filetype[PDF-385.53 KB]


Details:
  • Alternative Title:
    Prev Chronic Dis
  • Description:
    Introduction Hepatitis delta virus (HDV) is a serious coinfection of the hepatitis B virus (HBV) that is estimated to affect between 48 to 72 million people worldwide. Data are limited on the informational needs of people living with HDV. The Hepatitis B Foundation, a US-based nonprofit organization that provides support to people living with HBV and HDV, receives emails (queries) as part of a helpline, a service to provide information, resources, and support to people affected by HBV and HDV. Methods Query content was analyzed to assess the impact of HDV at the individual level. A total of 65 HDV-related queries from 17 countries were received from October 2016 to January 2019, and all were analyzed for this study. Results Thematic analysis of queries indicated 4 dominant themes. Three were related to a need for information about 1) the disease and prevention of it, 2) disease symptoms and outcomes, and 3) treatment options. The fourth theme was related to barriers and quality of life. Individuals requested information on treatment options, medication access, diagnostic test interpretation, and clinical trials. Conclusion Our study highlights the needs and lived experience of patients with HDV and summarizes critical information gaps. Findings can inform health care providers, public health professionals, and the pharmaceutical and biotechnology industries about the informational needs and lived experiences of individuals living with HDV and help create future HDV-related educational resources, care, and clinical trials.
  • Pubmed ID:
    33337297
  • Pubmed Central ID:
    PMC7769086
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