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Common concerns, barriers to care, and the lived experience of individuals with hepatitis B: a qualitative study
BACKGROUND: An estimated between 257 and 292 million people live with chronic HBV globally. While much is known about the causes, and epidemiology of HBV, little is understood about the quality of life and impact of HBV on those living with the infection. METHODS: A random sample of HBV-related emai...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8161662/ https://www.ncbi.nlm.nih.gov/pubmed/34044808 http://dx.doi.org/10.1186/s12889-021-11093-0 |
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author | Freeland, Catherine Farrell, Sean Kumar, Priyanka Kamischke, Maureen Jackson, Michaela Bodor, Sierra Block, Timothy M. Frasso, Rosemary Cohen, Chari |
author_facet | Freeland, Catherine Farrell, Sean Kumar, Priyanka Kamischke, Maureen Jackson, Michaela Bodor, Sierra Block, Timothy M. Frasso, Rosemary Cohen, Chari |
author_sort | Freeland, Catherine |
collection | PubMed |
description | BACKGROUND: An estimated between 257 and 292 million people live with chronic HBV globally. While much is known about the causes, and epidemiology of HBV, little is understood about the quality of life and impact of HBV on those living with the infection. METHODS: A random sample of HBV-related email queries sent to the Hepatitis B Foundation, a U.S.-based non-profit organization, over a 12-month period in 2018–2019 were retrieved, tabulated, and analyzed qualitatively to highlight information needs and explore the experiences of people living with HBV and their families and loved ones. Codebook development was informed by the literature and through line-by-line reading of a sub-sample of queries. Data analysis was facilitated by NVivo12 software. Data were coded independently by two members of the research team and intercoder reliability was assessed to assure coding accuracy throughout the coding phase. RESULTS: A total of 338 queries from people around the globe were identified and analyzed. The analysis revealed three thematic groups: 1) health-specific challenges associated with diagnosis and treatment, 2) emotional needs related to experiences with HBV stigma, discrimination, fear, social isolation, and distress and 3) informational needs related to HBV prevention and transmission, and interpretation of laboratory tests. CONCLUSIONS: People living with HBV are in need of information to manage their disease and prevent its spread. Analysis of queries uncovered significant misconceptions about HBV transmission and treatment. Additionally, the emotional and psychological impact of an HBV diagnosis on those living with the infection is significant. There is a clear need for patient and community education to expand knowledge and awareness of HBV globally to achieve 2030 WHO HBV elimination goals. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12889-021-11093-0. |
format | Online Article Text |
id | pubmed-8161662 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-81616622021-06-01 Common concerns, barriers to care, and the lived experience of individuals with hepatitis B: a qualitative study Freeland, Catherine Farrell, Sean Kumar, Priyanka Kamischke, Maureen Jackson, Michaela Bodor, Sierra Block, Timothy M. Frasso, Rosemary Cohen, Chari BMC Public Health Research BACKGROUND: An estimated between 257 and 292 million people live with chronic HBV globally. While much is known about the causes, and epidemiology of HBV, little is understood about the quality of life and impact of HBV on those living with the infection. METHODS: A random sample of HBV-related email queries sent to the Hepatitis B Foundation, a U.S.-based non-profit organization, over a 12-month period in 2018–2019 were retrieved, tabulated, and analyzed qualitatively to highlight information needs and explore the experiences of people living with HBV and their families and loved ones. Codebook development was informed by the literature and through line-by-line reading of a sub-sample of queries. Data analysis was facilitated by NVivo12 software. Data were coded independently by two members of the research team and intercoder reliability was assessed to assure coding accuracy throughout the coding phase. RESULTS: A total of 338 queries from people around the globe were identified and analyzed. The analysis revealed three thematic groups: 1) health-specific challenges associated with diagnosis and treatment, 2) emotional needs related to experiences with HBV stigma, discrimination, fear, social isolation, and distress and 3) informational needs related to HBV prevention and transmission, and interpretation of laboratory tests. CONCLUSIONS: People living with HBV are in need of information to manage their disease and prevent its spread. Analysis of queries uncovered significant misconceptions about HBV transmission and treatment. Additionally, the emotional and psychological impact of an HBV diagnosis on those living with the infection is significant. There is a clear need for patient and community education to expand knowledge and awareness of HBV globally to achieve 2030 WHO HBV elimination goals. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12889-021-11093-0. BioMed Central 2021-05-28 /pmc/articles/PMC8161662/ /pubmed/34044808 http://dx.doi.org/10.1186/s12889-021-11093-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Freeland, Catherine Farrell, Sean Kumar, Priyanka Kamischke, Maureen Jackson, Michaela Bodor, Sierra Block, Timothy M. Frasso, Rosemary Cohen, Chari Common concerns, barriers to care, and the lived experience of individuals with hepatitis B: a qualitative study |
title | Common concerns, barriers to care, and the lived experience of individuals with hepatitis B: a qualitative study |
title_full | Common concerns, barriers to care, and the lived experience of individuals with hepatitis B: a qualitative study |
title_fullStr | Common concerns, barriers to care, and the lived experience of individuals with hepatitis B: a qualitative study |
title_full_unstemmed | Common concerns, barriers to care, and the lived experience of individuals with hepatitis B: a qualitative study |
title_short | Common concerns, barriers to care, and the lived experience of individuals with hepatitis B: a qualitative study |
title_sort | common concerns, barriers to care, and the lived experience of individuals with hepatitis b: a qualitative study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8161662/ https://www.ncbi.nlm.nih.gov/pubmed/34044808 http://dx.doi.org/10.1186/s12889-021-11093-0 |
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