Hepatitis B Care and Treatment in Zanzibar, Tanzania: A Demonstration Project Following 2015 WHO Treatment Guidelines, 2017–2021
ABSTRACT Zanzibar, a low‐resource semiautonomous region of Tanzania, has an estimated prevalence of hepatitis B virus (HBV) infections of 3.6%. To assess the feasibility of care and treatment, a 5‐year hepatitis B demonstration project was implemented in Zanzibar during January 2017–December 2021, f...
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Veröffentlicht in: | Journal of viral hepatitis 2025-01, Vol.32 (1), p.e14051-n/a |
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description | ABSTRACT
Zanzibar, a low‐resource semiautonomous region of Tanzania, has an estimated prevalence of hepatitis B virus (HBV) infections of 3.6%. To assess the feasibility of care and treatment, a 5‐year hepatitis B demonstration project was implemented in Zanzibar during January 2017–December 2021, following the 2015 WHO HBV care and treatment guidelines. Participants included adults (aged ≥ 18 years) who tested positive for HBV surface antigen and tested negative for HIV and hepatitis C antibody. Participants were examined for clinical signs of liver disease and testing was conducted at baseline to assess treatment eligibility and every 6–12 months thereafter. Tenofovir disoproxil fumarate (TDF) was provided at no cost to treatment‐eligible participants. Clinical and laboratory data were analysed to assess improvement in proximal disease outcomes. Among 596 participants enrolled, the median age was 32 years (IQR 26–39) and 365 (61%) were male. Of those enrolled, 268 (45%) returned for ≥ 1 follow‐up visit, with a median of 511 days of follow‐up. Overall, 58 patients initiated treatment: 15 met treatment criteria based on liver cirrhosis alone; 13 by APRI > 1.5; among those with HBV DNA results, six met criteria based on HBV DNA levels and ALT activity; 24 met ≥ 2 criteria. Significant decreases in ALT activities, APRI scores and HBV DNA levels were observed among those treated. This hepatitis B care and treatment programme was demonstrated to be feasible in a low‐resource setting. Despite challenges, testing and linkage to care is critical to decrease the global burden of hepatitis B. |
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Zanzibar, a low‐resource semiautonomous region of Tanzania, has an estimated prevalence of hepatitis B virus (HBV) infections of 3.6%. To assess the feasibility of care and treatment, a 5‐year hepatitis B demonstration project was implemented in Zanzibar during January 2017–December 2021, following the 2015 WHO HBV care and treatment guidelines. Participants included adults (aged ≥ 18 years) who tested positive for HBV surface antigen and tested negative for HIV and hepatitis C antibody. Participants were examined for clinical signs of liver disease and testing was conducted at baseline to assess treatment eligibility and every 6–12 months thereafter. Tenofovir disoproxil fumarate (TDF) was provided at no cost to treatment‐eligible participants. Clinical and laboratory data were analysed to assess improvement in proximal disease outcomes. Among 596 participants enrolled, the median age was 32 years (IQR 26–39) and 365 (61%) were male. Of those enrolled, 268 (45%) returned for ≥ 1 follow‐up visit, with a median of 511 days of follow‐up. Overall, 58 patients initiated treatment: 15 met treatment criteria based on liver cirrhosis alone; 13 by APRI > 1.5; among those with HBV DNA results, six met criteria based on HBV DNA levels and ALT activity; 24 met ≥ 2 criteria. Significant decreases in ALT activities, APRI scores and HBV DNA levels were observed among those treated. This hepatitis B care and treatment programme was demonstrated to be feasible in a low‐resource setting. Despite challenges, testing and linkage to care is critical to decrease the global burden of hepatitis B.</description><identifier>ISSN: 1352-0504</identifier><identifier>ISSN: 1365-2893</identifier><identifier>EISSN: 1365-2893</identifier><identifier>DOI: 10.1111/jvh.14051</identifier><identifier>PMID: 39707980</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Adult ; Antiviral Agents - therapeutic use ; Cirrhosis ; Deoxyribonucleic acid ; DNA ; Female ; Hepatitis B ; Hepatitis B - diagnosis ; Hepatitis B - drug therapy ; Hepatitis B - epidemiology ; Hepatitis B Surface Antigens - blood ; Hepatitis B virus - drug effects ; Hepatitis B virus - genetics ; Hepatitis B, Chronic - diagnosis ; Hepatitis B, Chronic - drug therapy ; Hepatitis C ; Humans ; Liver diseases ; Male ; Middle Aged ; Practice Guidelines as Topic ; Prevalence ; Tanzania ; Tanzania - epidemiology ; Tenofovir ; Tenofovir - therapeutic use ; treatment ; World Health Organization ; Young Adult ; Zanzibar</subject><ispartof>Journal of viral hepatitis, 2025-01, Vol.32 (1), p.e14051-n/a</ispartof><rights>2024 John Wiley & Sons Ltd. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA.</rights><rights>Copyright © 2025 John Wiley & Sons Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0002-5772-7046</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjvh.14051$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjvh.14051$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39707980$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Said, Sanaa S.</creatorcontrib><creatorcontrib>Shadaker, Shaun</creatorcontrib><creatorcontrib>McMahon, Brian J.</creatorcontrib><creatorcontrib>Armstrong, Paige A.</creatorcontrib><creatorcontrib>Beckett, Geoff A.</creatorcontrib><creatorcontrib>Kamili, Saleem</creatorcontrib><creatorcontrib>Harris, Aaron M.</creatorcontrib><title>Hepatitis B Care and Treatment in Zanzibar, Tanzania: A Demonstration Project Following 2015 WHO Treatment Guidelines, 2017–2021</title><title>Journal of viral hepatitis</title><addtitle>J Viral Hepat</addtitle><description>ABSTRACT
Zanzibar, a low‐resource semiautonomous region of Tanzania, has an estimated prevalence of hepatitis B virus (HBV) infections of 3.6%. To assess the feasibility of care and treatment, a 5‐year hepatitis B demonstration project was implemented in Zanzibar during January 2017–December 2021, following the 2015 WHO HBV care and treatment guidelines. Participants included adults (aged ≥ 18 years) who tested positive for HBV surface antigen and tested negative for HIV and hepatitis C antibody. Participants were examined for clinical signs of liver disease and testing was conducted at baseline to assess treatment eligibility and every 6–12 months thereafter. Tenofovir disoproxil fumarate (TDF) was provided at no cost to treatment‐eligible participants. Clinical and laboratory data were analysed to assess improvement in proximal disease outcomes. Among 596 participants enrolled, the median age was 32 years (IQR 26–39) and 365 (61%) were male. Of those enrolled, 268 (45%) returned for ≥ 1 follow‐up visit, with a median of 511 days of follow‐up. Overall, 58 patients initiated treatment: 15 met treatment criteria based on liver cirrhosis alone; 13 by APRI > 1.5; among those with HBV DNA results, six met criteria based on HBV DNA levels and ALT activity; 24 met ≥ 2 criteria. Significant decreases in ALT activities, APRI scores and HBV DNA levels were observed among those treated. This hepatitis B care and treatment programme was demonstrated to be feasible in a low‐resource setting. Despite challenges, testing and linkage to care is critical to decrease the global burden of hepatitis B.</description><subject>Adult</subject><subject>Antiviral Agents - therapeutic use</subject><subject>Cirrhosis</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Female</subject><subject>Hepatitis B</subject><subject>Hepatitis B - diagnosis</subject><subject>Hepatitis B - drug therapy</subject><subject>Hepatitis B - epidemiology</subject><subject>Hepatitis B Surface Antigens - blood</subject><subject>Hepatitis B virus - drug effects</subject><subject>Hepatitis B virus - genetics</subject><subject>Hepatitis B, Chronic - diagnosis</subject><subject>Hepatitis B, Chronic - drug therapy</subject><subject>Hepatitis C</subject><subject>Humans</subject><subject>Liver diseases</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Practice Guidelines as Topic</subject><subject>Prevalence</subject><subject>Tanzania</subject><subject>Tanzania - epidemiology</subject><subject>Tenofovir</subject><subject>Tenofovir - therapeutic use</subject><subject>treatment</subject><subject>World Health Organization</subject><subject>Young Adult</subject><subject>Zanzibar</subject><issn>1352-0504</issn><issn>1365-2893</issn><issn>1365-2893</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2025</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkUtOHDEQhq0IFAjJIhdAltiwoAeXH_1gRyYZBoQEi4FI2bTc42rwqNs9sbtBZBXlCtyQk-DhpYhaVP1SfVUq1U_IV2AjiLG_uLkegWQKPpBNEKlKeF6ItZVWPGGKyQ3yKYQFYyC4go9kQxQZy4qcbZJ_U1zq3vY20G90rD1S7QydedR9i66n1tFf2v2xlfZ7dBaVdlYf0EP6HdvOhd7H4c7Rc98tcN7TSdc03a11V5QzUPTn9Oy_XUeDNdhYh2Fv1c4e_t5zxuEzWa91E_DLS90iF5Mfs_E0OT07Oh4fniZL4BIShRBPBjOfIy9yJXNtamVMpVQt65ggT4tcGqUrUQuOUqcolIC6Sg3mNRZii-w-71367veAoS9bG-bYNNphN4RSgMyKLIVCRHTnHbroBu_idSsqzySTPIvU9gs1VC2acultq_1d-frdCOw_A7e2wbu3PrByZVsZbSufbCtPLqdPQjwC13uIPQ</recordid><startdate>202501</startdate><enddate>202501</enddate><creator>Said, Sanaa S.</creator><creator>Shadaker, Shaun</creator><creator>McMahon, Brian J.</creator><creator>Armstrong, Paige A.</creator><creator>Beckett, Geoff A.</creator><creator>Kamili, Saleem</creator><creator>Harris, Aaron M.</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5772-7046</orcidid></search><sort><creationdate>202501</creationdate><title>Hepatitis B Care and Treatment in Zanzibar, Tanzania: A Demonstration Project Following 2015 WHO Treatment Guidelines, 2017–2021</title><author>Said, Sanaa S. ; Shadaker, Shaun ; McMahon, Brian J. ; Armstrong, Paige A. ; Beckett, Geoff A. ; Kamili, Saleem ; Harris, Aaron M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p1241-5e17981dcce298548adf5ddb55f4f55f186984d5ab3f32e4a6e3531fb6de8fe93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2025</creationdate><topic>Adult</topic><topic>Antiviral Agents - therapeutic use</topic><topic>Cirrhosis</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>Female</topic><topic>Hepatitis B</topic><topic>Hepatitis B - diagnosis</topic><topic>Hepatitis B - drug therapy</topic><topic>Hepatitis B - epidemiology</topic><topic>Hepatitis B Surface Antigens - blood</topic><topic>Hepatitis B virus - drug effects</topic><topic>Hepatitis B virus - genetics</topic><topic>Hepatitis B, Chronic - diagnosis</topic><topic>Hepatitis B, Chronic - drug therapy</topic><topic>Hepatitis C</topic><topic>Humans</topic><topic>Liver diseases</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Practice Guidelines as Topic</topic><topic>Prevalence</topic><topic>Tanzania</topic><topic>Tanzania - epidemiology</topic><topic>Tenofovir</topic><topic>Tenofovir - therapeutic use</topic><topic>treatment</topic><topic>World Health Organization</topic><topic>Young Adult</topic><topic>Zanzibar</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Said, Sanaa S.</creatorcontrib><creatorcontrib>Shadaker, Shaun</creatorcontrib><creatorcontrib>McMahon, Brian J.</creatorcontrib><creatorcontrib>Armstrong, Paige A.</creatorcontrib><creatorcontrib>Beckett, Geoff A.</creatorcontrib><creatorcontrib>Kamili, Saleem</creatorcontrib><creatorcontrib>Harris, Aaron M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of viral hepatitis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Said, Sanaa S.</au><au>Shadaker, Shaun</au><au>McMahon, Brian J.</au><au>Armstrong, Paige A.</au><au>Beckett, Geoff A.</au><au>Kamili, Saleem</au><au>Harris, Aaron M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hepatitis B Care and Treatment in Zanzibar, Tanzania: A Demonstration Project Following 2015 WHO Treatment Guidelines, 2017–2021</atitle><jtitle>Journal of viral hepatitis</jtitle><addtitle>J Viral Hepat</addtitle><date>2025-01</date><risdate>2025</risdate><volume>32</volume><issue>1</issue><spage>e14051</spage><epage>n/a</epage><pages>e14051-n/a</pages><issn>1352-0504</issn><issn>1365-2893</issn><eissn>1365-2893</eissn><abstract>ABSTRACT
Zanzibar, a low‐resource semiautonomous region of Tanzania, has an estimated prevalence of hepatitis B virus (HBV) infections of 3.6%. To assess the feasibility of care and treatment, a 5‐year hepatitis B demonstration project was implemented in Zanzibar during January 2017–December 2021, following the 2015 WHO HBV care and treatment guidelines. Participants included adults (aged ≥ 18 years) who tested positive for HBV surface antigen and tested negative for HIV and hepatitis C antibody. Participants were examined for clinical signs of liver disease and testing was conducted at baseline to assess treatment eligibility and every 6–12 months thereafter. Tenofovir disoproxil fumarate (TDF) was provided at no cost to treatment‐eligible participants. Clinical and laboratory data were analysed to assess improvement in proximal disease outcomes. Among 596 participants enrolled, the median age was 32 years (IQR 26–39) and 365 (61%) were male. Of those enrolled, 268 (45%) returned for ≥ 1 follow‐up visit, with a median of 511 days of follow‐up. Overall, 58 patients initiated treatment: 15 met treatment criteria based on liver cirrhosis alone; 13 by APRI > 1.5; among those with HBV DNA results, six met criteria based on HBV DNA levels and ALT activity; 24 met ≥ 2 criteria. Significant decreases in ALT activities, APRI scores and HBV DNA levels were observed among those treated. This hepatitis B care and treatment programme was demonstrated to be feasible in a low‐resource setting. Despite challenges, testing and linkage to care is critical to decrease the global burden of hepatitis B.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>39707980</pmid><doi>10.1111/jvh.14051</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-5772-7046</orcidid></addata></record> |
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subjects | Adult Antiviral Agents - therapeutic use Cirrhosis Deoxyribonucleic acid DNA Female Hepatitis B Hepatitis B - diagnosis Hepatitis B - drug therapy Hepatitis B - epidemiology Hepatitis B Surface Antigens - blood Hepatitis B virus - drug effects Hepatitis B virus - genetics Hepatitis B, Chronic - diagnosis Hepatitis B, Chronic - drug therapy Hepatitis C Humans Liver diseases Male Middle Aged Practice Guidelines as Topic Prevalence Tanzania Tanzania - epidemiology Tenofovir Tenofovir - therapeutic use treatment World Health Organization Young Adult Zanzibar |
title | Hepatitis B Care and Treatment in Zanzibar, Tanzania: A Demonstration Project Following 2015 WHO Treatment Guidelines, 2017–2021 |
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