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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
International Journal for Equity in Health volume 19, Article number: 156 (2020)
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.
Worldwide, 257 million people are infected with hepatitis B virus (HBV) with a mortality comparable to tuberculosis and higher than human immunodeficiency virus (HIV) and malaria [1, 2]. The United Nations Sustainable Development Goal 3.3 aims to combat viral hepatitis by 2030 through interruption of transmission by interventions on blood and injection safety, harm prevention strategies in people who inject drugs, and by prevention of mother to child transmission (PMTCT) .
In highly-endemic areas, such as sub-Saharan Africa and South East Asia, MTCT is the most important source of chronic HBV infection with vertical infections increasing the lifetime risk of developing liver fibrosis 5-fold compared with horizontally acquired infection [4, 5]. Hepatitis B immunoglobulin (HBIG) and hepatitis B birth dose (HepB-BD) monovalent vaccine followed by three doses of polyvalent vaccines provided in the expanded programme of immunization (EPI) have been the central strategies in high- and middle-income countries. Unfortunately, the opportunity to provide HBIG and HepB-BD in the first 12 h after birth is thwarted in resource-limited settings (RLS) due to a lack of essential health services especially facility births, a problem for half of the world’s population . Even with perfect implementation of HBIG and vaccination, 8–32% of infants can be infected via MTCT in HBeAg positive mothers [7, 8].
There is evidence from HIV that antivirals are safe and effective in prevention of MTCT in RLS in Africa and Asia [9,10,11,12]. Systematic review and meta-analysis report lamivudine, telbivudine and tenofovir disoproxil fumarate (tenofovir) provided in the third trimester can interrupt MTCT of HBV in hepatitis B e antigen (HBeAg) positive women with high HBV DNA > 106 IU/mL . Recent meta-analysis suggests better prevention of MTCT with telbivudine and tenofovir, and by initiation of antivirals before the third trimester . However the reduction of HBV DNA is highly dependent on starting viraemia and weeks of treatment with tenofovir. If HBV DNA is low at the time of delivery, HBIG may not be necessary, but the precise threshold of HBV DNA to forego HBIG is currently unknown [7, 14,15,16]. There are no HBV PMTCT studies where HBIG was not provided to the infant.
With the hypothesis that treatment with tenofovir commenced before an estimated gestational age (EGA) of 20 weeks will decrease the HBV DNA sufficiently to negate the need for HBIG, a study commenced in an area of high HBV prevalence among migrant and refugee women on the Thailand Myanmar border (ClinicalTrials.gov Identifier: NCT02995005). This commentary describes the challenges in a RLS with introduction of maternal tenofovir for PMTCT of HBV that will help future implementation of this strategy in similar settings.
The Thailand Myanmar border has a long and complex history of conflict and population movements. Since 1986 Shoklo Malaria Research Unit (SMRU) has provided humanitarian health care for refugees and since 1997 for migrants. Integrated to basic health care, SMRU has also conducted research on health problems of relevance to marginalized border population including antenatal and birthing services. Maternal and Child Health (MCH) services at SMRU are provided 24 h per day and attendance at antenatal care is voluntary with approximately 2500 new migrant pregnancies registered per year.
Brief description of PMTCT of HBV before the study
Screening pregnant women at the first antenatal visit for HBV has been routine at SMRU since 2012, but maternal antivirals for PMTCT of HBV is not supported by any organization. HIV screening has been conducted since 2001 with treatment currently provided by Myawaddy Government Hospital, Myanmar. In the migrant and refugee population on the Thailand Myanmar border the prevalence of hepatitis B among pregnant women is 6.2–8.3% [17, 18] and < 0.5% for HIV .
SMRU encourages all women to deliver with a skilled birth attendant in the clinic, decreasing the proportion of home deliveries to less than 15% for more than a decade which compares to 75% home deliveries in rural eastern Myanmar . For infants born in SMRU clinics, HepB-BD is provided in the first hours of life . HBIG has been available free of charge for HBeAg positive mothers when humanitarian funding has been sufficient. In most rural clinics in Myanmar, HBIG is not available and the cost of HBIG prohibitive: equivalent to 1 month salary for the average family . At SMRU in 2015, documentation of completion of the HepB-BD was higher than 90%, HBIG 76.5%, and infant EPI-3 doses, 55.1% .
Contrary to the border area, Thailand has a high proportion of hospital birth and a strong vaccination program under the Ministry of Public Health with the current Thailand National Guidelines stating that “HBsAg positive pregnant women should be started on tenofovir during pregnancy ”; and Myanmar’s first set of guidelines (July 2019) stating: “HBV mono-infected pregnant women who do not meet the criteria for treatment indications should receive tenofovir disoproxil fumarate (tenofovir) 300 mg once a day from 28 week of pregnancy until 3 months after delivery” . These tenofovir policies align with WHO standards that acknowledge usage of antiviral therapy for PMTCT of HBV , but there is no practice of them implemented in rural and RLS on either side of the Myanmar-Thailand border.
Brief description of the study
The tenofovir study is a one arm, open label, treatment intervention study, with a sample size of 170 non-Thai pregnant women (16–49 years old) with the primary aim to determine the viral kinetics of HBV DNA reduction in women following maternal tenofovir treatment in pregnancy . Women who meet the inclusion criteria (detectable HBV DNA, ultrasound confirmed viable singleton pregnancy, normal kidney function) can enroll at one of three sites along the Thailand-Myanmar border (Fig. 1). Women are provided with daily tenofovir starting between 12 to < 20 weeks’ EGA until 1 month after delivery, with continued follow-up at months 1, 2, 4 and 6 post-partum. The infant receives immunoprophylaxis including HepB-BD and EPI vaccination; and HBIG in HBeAg positive mothers.
At every pregnancy follow up, alanine aminotransferase (ALT) and creatinine are tested, and participants are asked about adherence using pill count and the ‘Adherence Starts with Knowledge’ questionnaire ASK-12 .
Identification of the challenges
In this commentary, we describe challenges that were encountered during the roll out of the tenofovir study in a RLS. Specific challenges were identified by reviewing the screening and enrolment logbooks to identify barriers to study inclusion of the migrant women that sought ANC care in our clinics. The pharmacy temperature logbooks were reviewed for medication storage, CRFs for comments about medication use, access and adherence by the study participants. Most importantly were the issues that were identified and clarified through discussions between health care workers and participants as they worked through monthly study visits. Missed study visits and missed medication were documented with reasons for these events described and recorded into the CRF. A full description of the study protocol including the consent was published previously . The health care staff involved in the study are part of the community themselves, with an extensive knowledge of the background, culture and language of local women.
This study has ethical approval from Mahidol Oxford Research Unit (FTM ECF-019-06), John Hopkins University (IRB No: 00007432), Chiang Mai University (FAM-2559-04227) and Oxford University (OxTREC Reference: 49–16) and the local Tak Community Advisory Board (TCAB-02/REV/2016).
The overall assessment of challenges was based on 171 pregnant women who were HBsAg positive by a point-of-care test (POCT) identified from 31 May 2018 until 31 Dec 2019. The challenges that were encountered were low awareness of HBV treatment for PMTCT, diagnostic limitations, constrained access to healthcare, risk of hepatic flare after cessation of tenofovir, and medication issues (Table 1).
Low awareness of HBV treatment for PMTCT
Although women on the Thailand Myanmar border are receptive to testing for infectious diseases in pregnancy with a near universal uptake of HBV point-of-care-testing (POCT), they still lack awareness of HBV treatment possibilities. In this study, 95.5% (84/88) of the HBsAg positive women with a singleton viable gestation below 20 weeks identified by POCT agreed for further blood investigations. This high uptake suggests a positive response to the concept of treatment of HBV, at least in the context of a study where there is support for study related costs such as transportation.
After general counseling about the infectious diseases that affect pregnancy and after obtaining informed consent, blood was tested for HBV, HIV, syphilis and malaria. Understanding and retention of knowledge from counseling sessions has not been formally tested for HBV in this population. The concern is that disease awareness may be limited by a lack of schooling as two-thirds of women at SMRU ANC did not finish 4th grade . The study is the first in this RLS to introduce the concept that HBV can be treated with drug therapy.
In summary, this study has not changed the already high uptake of HBV screening in pregnancy that was in place before study implementation, but the concept of treatment to prevent HBV transmission to the newborn is new information for local health staff and women. There is a need to measure the knowledge, attitudes and practices in relation to PMTCT of HBV to provide appropriate health messaging to pregnant women and their communities.
Identification of women that would benefit from tenofovir is challenging in RLS where the diagnosis relies on HBsAg rapid diagnostic tests and additional testing is not always available. In this study the Pacific Biotech POCT for HBsAg (reported sensitivity > 90% and specificity > 98% ) which uses a ‘gold standard’ chemiluminescent microparticle immunoassay had a proportion of false positive of 4/88, 4.5% (95% CI 0.2–8.9). A previous report using the same brand in the same population described a false positive proportion of 3.1% (95% CI 1.7–5.4) . This information is available because the study requires confirmation before treatment. In practice, approaches for HBV could consider using similar diagnostic criteria as for HIV, where two different POCT tests are sufficient to commence treatment,  which could lead to a more efficient test and treat policy. However, whether two different HBsAg POCT tests decreases the false positivity rate would need to be determined.
Maternal tenofovir is recommended, at least, for women with a high HBV DNA (> 200,000 IU/mL or HBeAg positive). Of the 84 HBsAg confirmed positive women 73/84 (86.9%) were eligible for the study: 23/73 (31.5%) were HBeAg positive. Women that were HBeAg negative were eligible if they tested positive (50/73, 68.5%) for the presence of HBV DNA (> 85 IU/mL) using a qualitative Polymerase Chain Reaction (PCR) test “HBV DNA assay Fast Track Diagnostics” (Siemens healthineers company). This study detected HBV DNA in HBeAg negative women with an off-site qualitative laboratory test that is expensive and is usually not available in RLSs .
In summary, the standard of HBsAg detection by a single POCT is insufficient to confidently identify women with HBsAg and further confirmation is needed.
Constrained access to healthcare
The ultimate goal of maternal tenofovir treatment for RLSs would be to reduce HBV DNA to undetectable levels to negate the necessity for HBIG at birth [30, 31]. In studies where tenofovir was initiated in third trimester, the HBV DNA was not reduced enough to reach this goal [7, 32]. Commencement of tenofovir in early pregnancy may reduce HBV DNA to undetectable levels before delivery and is the main reason for the current study. However, in RLSs, pregnant women often present after 20 weeks gestational age for antenatal care. As of 31 December 2019, 83/171 (48.5%) of the women in our ANC, who were HBsAg positive by POCT, presented after 20 weeks of pregnancy [18, 33].
In rural areas, participants face constraints on access to healthcare. They often live far away from the clinics and this implies that on some occasions these women need to walk for up to 4 h  to reach the clinic (Fig. 2). In their travels, most women have to cross one or more river systems, which show large seasonal variations with pronounced flooding (Fig. 3). Of the eight missed appointments in the tenofovir study, five (5/8, 62.5%) were in the rainy season when the rivers became impassable. Travel to the clinic also involves passage through police and/or military checkpoints on both sides of the border. In Thailand, there are documented and undocumented migrant workers with over a quarter of the migrant workers without work permits, or legal status, especially in rural areas. These migrant workers are at risk of being asked for additional fees, or of being arrested at police checkpoints, which can delay presentation with subsequent poorer outcomes. In this study a high follow up proportion of the expected appointments, 395/422 (93.6%) was obtained but women are assisted with transportation. Integrated care allowing pregnant women to complete HBV and ANC care in the same visit will reduce access constraints.
In summary, due to late ANC attendance only one in two women were eligible by gestation for the study. Integrated care alongside reducing access constraints in RLS remains a priority area for general improvement of maternal child health care. Despite difficulties women arrived for their appointments showing that mothers are motivated to overcome difficulties for the health of their pregnancy.
Risk of flare after cessation of antiviral therapy
After delivery, in RLSs, there is no support to continue HBV antivirals for the mother, should they be needed. Tenofovir treatment ceases 4–12 weeks post-partum and there is a risk for hepatic flare. Hepatic flares are detected using ALT but in most RLSs, ALT is not available on site which can cause a delay in identification of the flare. Most, 90%, of the cases resolves spontaneously, but in rare cases, flares could cause severe disease and even death [35, 36]. This implies that after stopping tenofovir treatment the woman should be able to follow up in a clinic preferably with the ability to measure ALT. In the study, 3/88 (3.4%) women were lost to follow up before the final check for hepatic flare. There was one patient that had a proven, asymptomatic, post-partum hepatic flare that resolved spontaneously after 5 months of additional follow up.
In summary the challenge of detection and management of hepatic flare after cessation of tenofovir post-partum requires careful discourse to ensure the woman remains safe. Flare can be detected and treated in RLS with an offsite laboratory but POCT for ALT would facilitate this.
Tenofovir should be taken once daily at a dosage of 300 mg. While monthly drug accountability checks have been high (94.6–100% adherence per follow up according to pill count and reviewers opinion), one in ten of the women reported incidents of tablet misplacement: “pills dropped though the [bamboo] floor and fell in the mud”, and “children played with the bottle”. The structure of typical households and the places where tablets are normally kept, such as plastic boxes or in an elevated shelf, is normal for families in these areas but may not be ideal or as safe as required (Figs. 4 and 5).
In Mae Sot (Fig. 1), the wet season is oppressive and overcast and the dry season is humid and hot. The highest relative humidity is in August (87%) and the lowest relative humidity in March (61%) . As an example in one of the study sites in 2019: the humidity averaged 76.1%  and for 187 days of the year the temperature was ≥30 °C, For 362/365 days (99.2%) humidity and ambient temperature (20-25 °C) were outside the manufacturer’s recommendations: tenofovir should be kept between 20 and 25 degrees Celsius (°C) . In this study medication is maintained at the required temperature via air-conditioning or refrigeration, and the study is monitored closely in line with Good Clinical Practice Guidelines . Participants are supplied with a maximum of 2 months of tenofovir at any one time in air tight resealable bottles of 30 tablets, complete with a silica gel sachet for absorption of moisture that is stored at room temperature as they do not own fridges. In the Gilead patent product information it states that “… tenofovir disoproxil fumarate is prone to decomposition at elevated humidities and temperatures” and the stability is also connected to the pH of the environment . Stability is likely to depend on the formulation of the tenofovir and products that are off patent and cheaper may not maintain the bioavailability or shelf life of the original product manufactured by Gilead.
In summary, most women appeared to manage their medications well but it should not be assumed that households have a safe storage place for medication. Study drugs were well maintained in fridges at the study field site and Gilead reports that Viread bioavailability is not affected by high average humidity and temperature. It is challenging for some women to adhere to good pharmacy practice in the household under normal tropical weather conditions, which may affect bioavailability in new, off-patent products.
The first step towards prevention of MTCT of hepatitis B is timely vaccination, which can be provided without screening for hepatitis B in pregnancy. This requires a minimum level of government investment in guidelines for policy and finance that supports this practice. Many RLS struggle to reach a high level of facility births, which impedes hepatitis B policy for both HepB-BD and HBIG. The window for prevention is small and is usually passed before home-born children come to the attention of service providers.
As early antenatal care remains a corner-stone to positive birth outcomes overall, not just early tenofovir, settings with late initiation of care can investigate the barriers to this at a local level. Nevertheless, more than 90% of pregnant women in RLS attend antenatal care, and screening for diseases transmitted from mother to child is a global practice. Therefore, adding HBsAg to this routine testing can boost awareness and help identify pregnant women at risk of transmitting to the newborn. Treatment options must be provided and explained as this can support or influence parental decisions of where a mother gives birth . Studies from RLS, and settings where literacy is limited, are required to clarify that antenatal care screening is understood.
Accurate POCTs are crucial to timely implementation of treatment. POCT for HBeAg and/or HBV DNA > 200,000 IU/mL would significantly boost identification of women who will benefit most from tenofovir. Offering treatment during pregnancy presents the highest profile of care for hepatitis B at the community level, just as it does for HIV. For RLS a critical question that requires an answer because health systems differ between resource-high and -limited settings is: Does tenofovir given in early pregnancy reduce the HBV DNA concentration to undetectable levels allowing the elimination of HBIG, which is unaffordable and difficult to maintain in RLS? This will be clarified when the tenofovir study results are analyzed.
Despite challenges, results from the study to date suggest tenofovir can be offered to HBV-infected women in RLS before 20 weeks gestation with a high uptake of screening, high drug accountability and follow-up, albeit with provision of transportation support related to the study. This commentary reports on a small and local study, but it is clear that mothers in RLS have the interest of their future offspring at heart and will go to serious efforts to obtain good outcomes. Governments and health service providers can take steps towards PMTCT of HBV by policies that are met with finance that ensure practice is harmonized towards the 2016 World Health Organization goal of viral hepatitis elimination by 2030.
Availability of data and materials
Data sharing is not applicable to this article as no datasets were generated or analysed during the current study.
Graber-Stiehl I. The silent epidemic killing more people than HIV, malaria or TB. Nature. 2018;564(7734):24–6.
Guidelines for the prevention, care and treatment of persons with chronic hepatitis B infection. Geneva: World Health Organization; 2015. Report No.: NLM classification: WC 536.” https://www.who.int/hepatitis/publications/hepatitis-b-guidelines/en/. Accessed 8 Jan 2020.
Thomas DL. Global elimination of chronic hepatitis. N Engl J Med. 2019;380(21):2041–50.
Shimakawa Y, Lemoine M, Njai HF, Bottomley C, Ndow G, Goldin RD, Jatta A, Jeng-Barry A, Wegmuller R, Moore SE, et al. Natural history of chronic HBV infection in West Africa: a longitudinal population-based study from the Gambia. Gut. 2016;65(12):2007–16.
Kramvis A. Challenges for hepatitis B virus cure in resource-limited settings in sub-Saharan Africa. Curr Opin HIV AIDS. 2020;15(3):185–92.
Bloom DE, Khoury A, Subbaraman R. The promise and peril of universal health care. Science. 2018;361:6404.
Pan CQ, Duan Z, Dai E, Zhang S, Han G, Wang Y, Zhang H, Zou H, Zhu B, Zhao W, et al. Tenofovir to prevent hepatitis B transmission in mothers with high viral load. N Engl J Med. 2016;374(24):2324–34.
Pan CQ, Duan ZP, Bhamidimarri KR, Zou HB, Liang XF, Li J, Tong MJ. An algorithm for risk assessment and intervention of mother to child transmission of hepatitis B virus. Clin Gastroenterol Hepatol. 2012;10(5):452–9.
Barditch-Crovo P, Deeks SG, Collier A, Safrin S, Coakley DF, Miller M, Kearney BP, Coleman RL, Lamy PD, Kahn JO, et al. Phase i/ii trial of the pharmacokinetics, safety, and antiretroviral activity of tenofovir disoproxil fumarate in human immunodeficiency virus-infected adults. Antimicrob Agents Chemother. 2001;45(10):2733–9.
Brown RS Jr, McMahon BJ, Lok AS, Wong JB, Ahmed AT, Mouchli MA, Wang Z, Prokop LJ, Murad MH, Mohammed K. Antiviral therapy in chronic hepatitis B viral infection during pregnancy: a systematic review and meta-analysis. Hepatology. 2016;63(1):319–33.
Ogawa E, Furusyo N, Nguyen MH. Tenofovir alafenamide in the treatment of chronic hepatitis B: design, development, and place in therapy. Drug Des Devel Ther. 2017;11:3197–204.
Vrazo AC, Sullivan D, Ryan Phelps B. Eliminating mother-to-child transmission of HIV by 2030: 5 strategies to ensure continued Progress. Glob Health Sci Pract. 2018;6(2):249–56.
Wu Y, Liu J, Feng Y, Fu S, Ji F, Ge L, Yao N, Luo X, Zhao Y, Chen Y, et al. Efficacy and safety of antiviral therapy for HBV in different trimesters of pregnancy: systematic review and network meta-analysis. Hepatol Int. 2020;14(2):180–9.
Hyun MH, Lee YS, Kim JH, Je JH, Yoo YJ, Yeon JE, Byun KS. Systematic review with meta-analysis: the efficacy and safety of tenofovir to prevent mother-to-child transmission of hepatitis B virus. Aliment Pharmacol Ther. 2017;45(12):1493–505.
Celen MK, Mert D, Ay M, Dal T, Kaya S, Yildirim N, Gulsun S, Barcin T, Kalkanli S, Dal MS, et al. Efficacy and safety of tenofovir disoproxil fumarate in pregnancy for the prevention of vertical transmission of HBV infection. World J Gastroenterol. 2013;19(48):9377–82.
Chen HL, Lee CN, Chang CH, Ni YH, Shyu MK, Chen SM, Hu JJ, Lin HH, Zhao LL, Mu SC, et al. Efficacy of maternal tenofovir disoproxil fumarate in interrupting mother-to-infant transmission of hepatitis B virus. Hepatology. 2015;62(2):375–86.
Banks T, Kang J, Watts I, Tyrosvoutis ME, Min AM, Tun NW, Keereecharoen L, Simmawong W, Wanyatip S, Hanboonkunupakarn B, et al. High hepatitis B seroprevalence and risk factors for infection in pregnant women on the Thailand-Myanmar border. J Infect Dev Ctries. 2016;10(4):384–8.
Bierhoff M, Angkurawaranon C, Myat Min A, Gilder ME, Win Tun N, Keereevijitt A, Kyi Win A, Win E, Carrara VI, Brummaier T, et al. Maternal hepatitis B infection burden, comorbidity and pregnancy outcome in a low-income population on the Myanmar-Thailand border: a retrospective cohort study. J Pregnancy. 2019;2019:8435019.
Plewes K, Lee T, Kajeechewa L, Thwin MM, Lee SJ, Carrara VI, Nosten F, McGready R. Low seroprevalence of HIV and syphilis in pregnant women in refugee camps on the Thai-Burma border. Int J STD AIDS. 2008;19(12):833–7.
Bierhoff M, Pinyopornpanish K, Pinyopornpanish K, Tongprasert F, Keereevijit A, Rijken M, Chu CS, Nosten F, Perfetto J, van Vugt M, et al. Retrospective review of documentation practices of hepatitis B immunoglobulin, birth dose, and vaccination at the hospital of birth, in Thai nationals and migrants in Northern Thailand. Open Forum Infect Dis. 2019;6(12):ofz518.
O'Hara GA, McNaughton AL, Maponga T, Jooste P, Ocama P, Chilengi R, Mokaya J, Liyayi MI, Wachira T, Gikungi DM, et al. Hepatitis B virus infection as a neglected tropical disease. PLoS Negl Trop Dis. 2017;11(10):e0005842.
Thailand Practice Guideline for Management of Chronic Hepatitis B and C 2015 http://www.thasl.org/files/25.Thailand%20guideline%20for%20management%20of%20CHB%20%20and%20CHC%202015.pdf. Accessed 18 Feb 2020.
Ministry of Health and Sports Myanmar. National simplified treatment guidelines of viral hepatitis B infection. In: National hepatitis control program; 2019.
Bierhoff M, Guo N, Jia Y, Angkurawaranon C, Jittamala P, Carrara VI, Watthanaworawit W, Ling CL, Tongprasert F, van Vugt M, Rijken MJ, Nosten F, McGready R, Ehrhardt S, Thio CL. Prevention of mother-to-child transmission of hepatitis B virus: protocol for a one arm, open label intervention study to estimate the optimal timing of tenofovir in pregnancy. BMJ Open. 2020; in press.
Sasaki J, Kawayama T, Yoshida M, Takahashi K, Fujii K, Machida K, Kinoshita T, Hoshino T. Adherence barriers to inhaled medicines in Japanese older patients with asthma evaluated using the “Adherence Starts with Knowledge 20” (ASK-20) questionnaire. J Asthma. 2019;56(6):632–41.
Gilder ME, Moo P, Hashmi A, Praisaengdet N, Wai K, Pimanpanarak M, Carrara VI, Angkurawaranon C, Jiraporncharoen W, McGready R. “I can’t read and don’t understand”: health literacy and health messaging about folic acid for neural tube defect prevention in a migrant population on the Myanmar-Thailand border. PLoS One. 2019;14(6):e0218138.
Amini A, Varsaneux O, Kelly H, Tang W, Chen W, Boeras DI, Falconer J, Tucker JD, Chou R, Ishizaki A, et al. Diagnostic accuracy of tests to detect hepatitis B surface antigen: a systematic review of the literature and meta-analysis. BMC Infect Dis. 2017;17(Suppl 1):698.
Mayaphi SH, Martin DJ, Quinn TC, Laeyendecker O, Olorunju SA, Tintinger GR, Stoltz AC. Detection of acute and early HIV-1 infections in an HIV hyper-endemic area with limited resources. PLoS One. 2016;11(10):e0164943.
Ishizaki A, Bouscaillou J, Luhmann N, Liu S, Chua R, Walsh N, Hess S, Ivanova E, Roberts T, Easterbrook P. Survey of programmatic experiences and challenges in delivery of hepatitis B and C testing in low- and middle-income countries. BMC Infect Dis. 2017;17(Suppl 1):696.
Thio CL, Guo N, Xie C, Nelson KE, Ehrhardt S. Global elimination of mother-to-child transmission of hepatitis B: revisiting the current strategy. Lancet Infect Dis. 2015;15(8):981–5.
Wang M, Bian Q, Zhu Y, Pang Q, Chang L, Li R, Tiongson BC, Zhang H, Pan CQ. Real-world study of tenofovir disoproxil fumarate to prevent hepatitis B transmission in mothers with high viral load. Aliment Pharmacol Ther. 2019;49(2):211–7.
Wang J, Liu J, Qi C, Yan T, Cao F, Jin L, He Y, Yang Y, Zhang S, Chen T, et al. Efficacy of tenofovir disoproxil fumarate to prevent vertical transmission in mothers with lamivudine-resistant HBV. Antivir Ther. 2015;20(7):681–7.
Gross K, Alba S, Glass TR, Schellenberg JA, Obrist B. Timing of antenatal care for adolescent and adult pregnant women in south-eastern Tanzania. BMC Pregnancy Childbirth. 2012;12:16.
Thaddeus S, Maine D. Too far to walk: maternal mortality in context. Soc Sci Med. 1994;38(8):1091–110.
Nguyen V, Tan PK, Greenup AJ, Glass A, Davison S, Samarasinghe D, Holdaway S, Strasser SI, Chatterjee U, Jackson K, et al. Anti-viral therapy for prevention of perinatal HBV transmission: extending therapy beyond birth does not protect against post-partum flare. Aliment Pharmacol Ther. 2014;39(10):1225–34.
Chang M-L, Liaw Y-F. Hepatitis B flares in chronic hepatitis B: pathogenesis, natural course, and management. J Hepatol. 2014;61(6):1407–17.
Average humidity Mae Sot, Thailand. https://www.weather-th.com/en/thailand/mae-sot-climate#humidity_relative. Accessed 14 Jan 2020.
Summary of product characteristics. https://www.ema.europa.eu/en/documents/product-information/viread-epar-product-information_en.pdf. Accessed 14 Jan 2020.
ICH Harmonised Guideline Integrated Addendum to ICH E6(R1): Guideline for good clinical practice ICH E6(R2) ICH consensus guideline. https://ichgcp.net/. Accessed 14 Jan 2020.
A stable pharmaceutical composition containing tenofovir disoproxil fumarate https://patents.google.com/patent/WO2015085976A1/en. Accessed 14 Jan 2020.
Tschirhart N, Jiraporncharoen W, Angkurawaranon C, Hashmi A, Nosten S, McGready R, Ottersen T. Choosing where to give birth: factors influencing migrant women’s decision making in two regions of Thailand. PLoS One. 2020;15(4):e0230407.
We would kindly like to acknowledge all contributions of SMRU staff and doctors for their help in implementing this strategy. Suphak Nosten and Saw Chrishes for the beautiful pictures.
The work is supported by the following awards: Thrasher Research Fund [grant number: TRF13096] to Johns Hopkins University; the Wellcome-Trust Major Overseas Program in Southeast Asia [grant number: 106698/Z/14/Z] to Mahidol University Oxford Tropical Medicine Research Programme which directly supports FN and RM from Shoklo Malaria Research Unit; and Chiang Mai University Thailand supporting MB and CA.
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Bierhoff, M., Rijken, M.J., Yotyingaphiram, W. et al. 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. Int J Equity Health 19, 156 (2020). https://doi.org/10.1186/s12939-020-01268-3
- Antiviral therapy