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dc.contributor.authorM. Bierhoffen_US
dc.contributor.authorM. J. Rijkenen_US
dc.contributor.authorW. Yotyingaphiramen_US
dc.contributor.authorM. Pimanpanaraken_US
dc.contributor.authorM. Van Vugten_US
dc.contributor.authorC. Angkurawaranonen_US
dc.contributor.authorF. Nostenen_US
dc.contributor.authorS. Ehrhardten_US
dc.contributor.authorC. L. Thioen_US
dc.contributor.authorR. McGreadyen_US
dc.date.accessioned2020-10-14T08:40:57Z-
dc.date.available2020-10-14T08:40:57Z-
dc.date.issued2020-09-10en_US
dc.identifier.issn14759276en_US
dc.identifier.other2-s2.0-85090817581en_US
dc.identifier.other10.1186/s12939-020-01268-3en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85090817581&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/70765-
dc.description.abstract© 2020 The Author(s). Background: The aim of this manuscript is to highlight challenges in the implementation of maternal tenofovir disoproxil fumarate (tenofovir) for prevention of mother to child transmission (PMTCT) of hepatitis B virus (HBV) in resource limited setting. Current preventive strategies in resource-limited settings fail mainly due to prohibitive costs of hepatitis B immunoglobulin (HBIG) and a high proportion of homebirths, meaning both HBIG and hepatitis B birth dose vaccine are not given. A new strategy for PMTCT without the necessity of HBIG, could be daily tenofovir commenced early in gestation. Implementation challenges to early tenofovir for PMTCT can provide insight to elimination strategies of HBV as the burden of disease is high in resource-limited settings. Methods: Challenges encountered during implementation of a study of tenofovir for PMTCT before 20 weeks gestation in rural and resource-limited areas on the Thailand-Myanmar border were identified informally from trial study logbooks and formally from comments from patients and staff at monthly visits. ClinicalTrials.gov Identifier: NCT02995005. Main body: During implementation 171 pregnant women were hepatitis B surface antigen (HBsAg) positive by point of-care test over 19 months (May-2018 until Dec-2019). In this resource-limited setting where historically no clinic has provided tenofovir for PMTCT of HBV, information provided by staff resulted in a high uptake of study screening (95.5% (84/88) when offered to pregnant women. False positive point-of-care rapid tests hinder a test and treat policy for HBV and development of improved rapid tests that include HBeAg and/or HBV DNA would increase efficiency. Integrated care of HBV to antenatal care, transport assistance and local agreements to facilitate access, could increase healthcare at this critical stage of the life course. As safe storage of medication in households in resource-limited setting may not be ideal, interactive counseling about this must be a routine part of care. Conclusion: Despite challenges, results from the study to date suggest tenofovir can be offered to HBV-infected women in resource-limited settings before 20 weeks gestation with a high uptake of screening, high drug accountability and follow-up, with provision of transportation support. This commentary has highlighted practical implementation issues with suggestions for strategies that support the objective of PMTCT and the World Health Organization goal of HBV elimination by 2030.en_US
dc.subjectMedicineen_US
dc.titleTenofovir for prevention of mother to child transmission of hepatitis B in migrant women in a resource-limited setting on the Thailand-Myanmar border: A commentary on challenges of implementationen_US
dc.typeJournalen_US
article.title.sourcetitleInternational Journal for Equity in Healthen_US
article.volume19en_US
article.stream.affiliationsShoklo Malaria Research Uniten_US
article.stream.affiliationsUniversity Medical Center Utrechten_US
article.stream.affiliationsNuffield Department of Medicineen_US
article.stream.affiliationsJohns Hopkins Bloomberg School of Public Healthen_US
article.stream.affiliationsUniversiteit van Amsterdamen_US
article.stream.affiliationsJohns Hopkins School of Medicineen_US
article.stream.affiliationsChiang Mai Universityen_US
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