{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,27]],"date-time":"2026-10-27T14:55:25Z","timestamp":1793112925012,"version":"4.5.0"},"reference-count":50,"publisher":"SAGE Publications","license":[{"start":{"date-parts":[[2023,1,1]],"date-time":"2023-01-01T00:00:00Z","timestamp":1672531200000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["Journal of Patient Experience"],"published-print":{"date-parts":[[2023,1]]},"abstract":"<jats:p>Living with chronic hepatitis B (CHB) has physical, social, and emotional impacts that often negatively affect patients\u2019 quality of life. These impacts are not usually captured during routine care. This article presents information on the impact of living with CHB and the importance of integrating health-related quality-of-life assessment into CHB care. Using a global online survey, people ages \u226518 living with CHB were asked about physical, social, and worry impacts. Of 1707 respondents, most were male (67%),\u2009&lt;\u200945 years of age (81%); and 52% identified as Black. Of all participants, 66% reported physical impact, 55% reported social impact, and 49% reported worry impact of living with CHB. Those from Africa and the Western Pacific were most likely to report physical impact. Younger participants (18-45) and those not on treatment were significantly more likely to report physical and social impact. People living with CHB are impacted physically, socially, and emotionally, varied by demographic factors and disease experience. These impacts should be captured and addressed as part of routine CHB care.<\/jats:p>","DOI":"10.1177\/23743735231211069","type":"journal-article","created":{"date-parts":[[2023,11,13]],"date-time":"2023-11-13T18:09:06Z","timestamp":1699898946000},"update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":16,"title":["The Impact of Living With Chronic Hepatitis B on Quality of Life: Implications for Clinical Management"],"prefix":"10.1177","volume":"10","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-4451-8488","authenticated-orcid":false,"given":"Yasmin","family":"Ibrahim","sequence":"first","affiliation":[{"name":"Hepatitis B Foundation, Doylestown, Pennsylvania, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Madeleine","family":"Umstead","sequence":"additional","affiliation":[{"name":"Hepatitis B Foundation, Doylestown, Pennsylvania, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Su","family":"Wang","sequence":"additional","affiliation":[{"name":"Former President of World Hepatitis Alliance, London, UK"},{"name":"Center for Asian Health & Viral Hepatitis Programs, Cooperman Barnabas Medical Center, Florham Park, New Jersey, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Chari","family":"Cohen","sequence":"additional","affiliation":[{"name":"Hepatitis B Foundation, Doylestown, Pennsylvania, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"179","published-online":{"date-parts":[[2023,11,13]]},"reference":[{"key":"bibr1-23743735231211069","doi-asserted-by":"publisher","DOI":"10.1016\/S2468-1253(22)00124-8"},{"key":"bibr2-23743735231211069","doi-asserted-by":"publisher","DOI":"10.1002\/hep.24199"},{"key":"bibr3-23743735231211069","doi-asserted-by":"publisher","DOI":"10.1016\/j.jhep.2011.12.001"},{"key":"bibr4-23743735231211069","doi-asserted-by":"publisher","DOI":"10.1002\/hep.28280"},{"key":"bibr5-23743735231211069","doi-asserted-by":"publisher","DOI":"10.1586\/egh.09.65"},{"key":"bibr6-23743735231211069","doi-asserted-by":"publisher","DOI":"10.1111\/j.1365-2893.2007.00895.x"},{"key":"bibr7-23743735231211069","unstructured":"Cohen C, Block J, Ibrahim Y, The Hepatitis B Foundation. 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