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dc.contributor.authorMarieke Bierhoffen_US
dc.contributor.authorChaisiri Angkurawaranonen_US
dc.contributor.authorMarcus J. Rijkenen_US
dc.contributor.authorKanlaya Sriprawaen_US
dc.contributor.authorPachinee Kobphanen_US
dc.contributor.authorFrancois N. Nostenen_US
dc.contributor.authorMichèle van Vugten_US
dc.contributor.authorRose McGreadyen_US
dc.contributor.authorAngela Devineen_US
dc.date.accessioned2022-10-16T07:20:42Z-
dc.date.available2022-10-16T07:20:42Z-
dc.date.issued2021-12-01en_US
dc.identifier.issn14712393en_US
dc.identifier.other2-s2.0-85101307796en_US
dc.identifier.other10.1186/s12884-021-03612-zen_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85101307796&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/76948-
dc.description.abstractBackground: Hepatitis B Virus (HBV) is transmitted from mother to child which can be prevented via birth dose vaccine combined with three follow up hepatitis B vaccines, hepatitis B immunoglobulins (HBIG), and maternal antiviral treatment with Tenofovir Disoproxil Fumarate (TDF). This study evaluates the cost effectiveness of six strategies to prevent perinatal HBV transmission in a resource limited setting (RLS) on the Thailand-Myanmar border. Methods: The cost effectiveness of six strategies was tested by a decision tree model in R. All strategies included birth and follow up vaccinations and compared cost per infection averted against two willingness to pay thresholds: one-half and one gross domestic product (GDP) per capita. Strategies were: 1) Vaccine only, 2) HBIG after rapid diagnostic test (RDT): infants born to HBsAg+ are given HBIG, 3) TDF after RDT: HBsAg+ women are given TDF, 4) TDF after HBeAg test: HBeAg+ women are given TDF, 5) TDF after high HBV DNA: women with HBV DNA > 200,000 are given TDF, 6) HBIG & TDF after high HBV DNA: women with HBV DNA > 200,000 are given TDF and their infants are given HBIG. One-way and probabilistic sensitivity analyses were conducted on the cost-effective strategies. Results: Vaccine only was the least costly option with TDF after HBeAg test strategy as the only cost-effective alternative. TDF after HBeAg test had an incremental cost-effectiveness ratio of US$1062; which would not be considered cost-effective with the lower threshold of one-half GDP per capita. The one-way sensitivity analysis demonstrated that the results were reasonably robust to changes in single parameter values. The PSA showed that TDF after HBeAg test had an 84% likelihood of being cost effective at a willingness to pay threshold of one GDP per capita per infection averted. Conclusions: We found that TDF after HBeAg test has the potential to be cost-effective if TDF proves effective locally to prevent perinatal HBV transmission. The cost of TDF treatment and reliability of the RDT could be barriers to implementing this strategy. While TDF after RDT may be a more feasible strategy to implement in RLS, TDF after HBeAg test is a less costly option.en_US
dc.subjectMedicineen_US
dc.titleTenofovir disoproxil fumarate in pregnancy for prevention of mother to child transmission of hepatitis B in a rural setting on the Thailand-Myanmar border: a cost-effectiveness analysisen_US
dc.typeJournalen_US
article.title.sourcetitleBMC Pregnancy and Childbirthen_US
article.volume21en_US
article.stream.affiliationsMelbourne School of Population and Global Healthen_US
article.stream.affiliationsMenzies School of Health Researchen_US
article.stream.affiliationsMahidol Universityen_US
article.stream.affiliationsNuffield Department of Medicineen_US
article.stream.affiliationsUniversiteit van Amsterdamen_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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