Tenofovir 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 implementation.


Journal

International journal for equity in health
ISSN: 1475-9276
Titre abrégé: Int J Equity Health
Pays: England
ID NLM: 101147692

Informations de publication

Date de publication:
10 09 2020
Historique:
received: 27 04 2020
accepted: 25 08 2020
entrez: 11 9 2020
pubmed: 12 9 2020
medline: 23 1 2021
Statut: epublish

Résumé

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. 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. 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. 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.

Sections du résumé

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.

Identifiants

pubmed: 32912268
doi: 10.1186/s12939-020-01268-3
pii: 10.1186/s12939-020-01268-3
pmc: PMC7488314
doi:

Substances chimiques

Antiviral Agents 0
Hepatitis B Surface Antigens 0
Hepatitis B Vaccines 0
Hepatitis B e Antigens 0
Immunoglobulins 0
Tenofovir 99YXE507IL
hepatitis B hyperimmune globulin XII270YC6M

Banques de données

ClinicalTrials.gov
['NCT02995005']

Types de publication

Letter Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

156

Subventions

Organisme : Wellcome Trust
ID : 106698/Z/14/Z
Pays : United Kingdom

Références

Hepatology. 2016 Jan;63(1):319-33
pubmed: 26565396
PLoS One. 2016 Oct 20;11(10):e0164943
pubmed: 27764165
Curr Opin HIV AIDS. 2020 May;15(3):185-192
pubmed: 32141888
Hepatol Int. 2020 Mar;14(2):180-189
pubmed: 32193814
Aliment Pharmacol Ther. 2017 Jun;45(12):1493-1505
pubmed: 28436552
Clin Gastroenterol Hepatol. 2012 May;10(5):452-9
pubmed: 22079509
Gut. 2016 Dec;65(12):2007-2016
pubmed: 26185161
Science. 2018 Aug 24;361(6404):
pubmed: 30139847
J Hepatol. 2014 Dec;61(6):1407-17
pubmed: 25178562
Antivir Ther. 2015;20(7):681-7
pubmed: 26215771
BMC Pregnancy Childbirth. 2012 Mar 21;12:16
pubmed: 22436344
BMC Infect Dis. 2017 Nov 1;17(Suppl 1):698
pubmed: 29143619
J Asthma. 2019 Jun;56(6):632-641
pubmed: 29969920
Antimicrob Agents Chemother. 2001 Oct;45(10):2733-9
pubmed: 11557462
Hepatology. 2015 Aug;62(2):375-86
pubmed: 25851052
Int J STD AIDS. 2008 Dec;19(12):833-7
pubmed: 19050214
Soc Sci Med. 1994 Apr;38(8):1091-110
pubmed: 8042057
N Engl J Med. 2019 May 23;380(21):2041-2050
pubmed: 31116920
Open Forum Infect Dis. 2019 Dec 07;6(12):ofz518
pubmed: 31890723
Glob Health Sci Pract. 2018 Jun 29;6(2):249-256
pubmed: 29959270
Aliment Pharmacol Ther. 2019 Jan;49(2):211-217
pubmed: 30506691
J Pregnancy. 2019 Feb 25;2019:8435019
pubmed: 30931155
World J Gastroenterol. 2013 Dec 28;19(48):9377-82
pubmed: 24409065
PLoS One. 2019 Jun 13;14(6):e0218138
pubmed: 31194796
Nature. 2018 Dec;564(7734):24-26
pubmed: 30518904
J Infect Dev Ctries. 2016 Apr 28;10(4):384-8
pubmed: 27131000
BMC Infect Dis. 2017 Nov 1;17(Suppl 1):696
pubmed: 29143609
Aliment Pharmacol Ther. 2014 May;39(10):1225-34
pubmed: 24666381
PLoS One. 2020 Apr 2;15(4):e0230407
pubmed: 32240176
N Engl J Med. 2016 Jun 16;374(24):2324-34
pubmed: 27305192
Lancet Infect Dis. 2015 Aug;15(8):981-5
pubmed: 26145195
Drug Des Devel Ther. 2017 Nov 06;11:3197-3204
pubmed: 29158666
PLoS Negl Trop Dis. 2017 Oct 5;11(10):e0005842
pubmed: 28981505

Auteurs

M Bierhoff (M)

Shoklo Malaria Research Unit, Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Mae Sot, 63110, Thailand. mariekebierhoff@yahoo.com.
Division of Infectious Diseases, Academic UMC, University of Amsterdam, Amsterdam, The Netherlands. mariekebierhoff@yahoo.com.

M J Rijken (MJ)

Department of Obstetrics and Gynaecology, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands.
Julius Global Health, The Julius Centre for Health Sciences, University Medical Centre Utrecht, Utrecht, Netherlands.

W Yotyingaphiram (W)

Shoklo Malaria Research Unit, Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Mae Sot, 63110, Thailand.

M Pimanpanarak (M)

Shoklo Malaria Research Unit, Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Mae Sot, 63110, Thailand.

M van Vugt (M)

Division of Infectious Diseases, Academic UMC, University of Amsterdam, Amsterdam, The Netherlands.

C Angkurawaranon (C)

Department of Family Medicine, Faculty of Medicine, Chiang Mai University, Chiang Mai, 50200, Thailand.

F Nosten (F)

Shoklo Malaria Research Unit, Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Mae Sot, 63110, Thailand.
Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine Research Building, University of Oxford, Oxford, UK.

S Ehrhardt (S)

Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.

C L Thio (CL)

Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

R McGready (R)

Shoklo Malaria Research Unit, Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Mae Sot, 63110, Thailand.
Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine Research Building, University of Oxford, Oxford, UK.

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