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

被引:12
作者
Bierhoff, Marieke [1 ,2 ]
Nelson, Kenrad E. [3 ]
Guo, Nan [4 ]
Jia, Yuanxi [3 ]
Angkurawaranon, Chaisiri [5 ]
Jittamala, Podjanee [6 ,7 ]
Carrara, Verena [1 ,8 ]
Watthanaworawit, Wanitda [9 ]
Ling, Clare [8 ,9 ]
Tongprasert, Fuanglada [10 ]
van Vugt, Michele [2 ]
Rijken, Marcus [11 ]
Nosten, Francois [1 ]
McGready, Rose [1 ]
Ehrhardt, Stephan [3 ]
Thio, Chloe Lynne [12 ]
机构
[1] Mahidol Univ, Mahidol Oxford Trop Med Res Unit, Dept Maternal & Child Hlth, Shoklo Malaria Res Unit,Fac Trop Med, Mae Sot, Thailand
[2] Univ Amsterdam, Dept Infect Dis, Ctr Trop Med & Travel Med, Amsterdam UMC,Internal Med, Amsterdam, Netherlands
[3] Johns Hopkins Univ, Dept Epidemiol, Baltimore, MD 21218 USA
[4] Stanford Univ, Dept Anesthesiol Perioperat & Pain Med, Stanford, CA 94305 USA
[5] Chiang Mai Univ, Dept Family Med, Chiang Mai, Thailand
[6] Mahidol Univ, Fac Trop Med, Dept Maternal & Child Hlth, Mahidol Oxford Trop Med Res Unit, Bangkok, Thailand
[7] Mahidol Univ, Dept Trop Hyg, Fac Med, Ramathibodi Hosp, Bangkok, Thailand
[8] Univ Oxford, Ctr Trop Med & Global Hlth, Oxford, England
[9] Mahidol Univ, Fac Trop Med, Mahidol Oxford Trop Med Res Unit, Shoklo Malaria Res Unit,Dept Microbiol, Mae Sot, Thailand
[10] Chiang Mai Univ, Dept Obstet & Gynecol, Chiang Mai, Thailand
[11] Univ Utrecht, Dept Obstet & Gynecol, Utrecht, Netherlands
[12] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
关键词
public health; tropical medicine; fetal medicine; maternal medicine; therapeutics; virology; DISOPROXIL FUMARATE; GLOBAL ELIMINATION; MIGRANT WORKERS; VIRAL LOAD; PHARMACOKINETICS; INFECTION; THAILAND; SAFETY; VACCINATION; EFFICACY;
D O I
10.1136/bmjopen-2020-038123
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Hepatitis B virus (HBV) remains a public health threat and the main route of transmission is from mother to child (MTCT). Tenofovir disoproxil fumarate (TDF) treatment can reduce MTCT of HBV although the optimal timing to attain undetectable HBV DNA concentrations at delivery is unknown. This protocol describes the procedures following early initiation of maternal TDF prior to 20 weeks gestation to determine efficacy, safety and feasibility of this approach in a limited-resource setting. Methods and analyses One hundred and seventy pregnant women from the Thailand-Myanmar border between 12 and <20 weeks gestational age will be enrolled into a one-arm, open-label, TDF treatment study with cessation of TDF 1 month after delivery. Sampling occurs monthly prenatal, at birth and at 1, 2, 4 and 6 months post partum. Measurement of tenofovir concentrations in maternal and cord plasma is anticipated in 10-15 women who have detectable HBV DNA at delivery and matched to 20-30 women with no detectable HBV DNA. Infant HBsAg status will be determined at 2 months of age and HBV DNA confirmed in HBsAg positive cases. Adverse events including risk of flare and adherence, based on pill count and questionnaire, will be monitored. Infants will receive HBV vaccinations at birth, 2, 4 and 6 months and hepatitis B immunoglobulin at birth if the mother is hepatitis B e antigen positive. Infant growth and neurodevelopment at 6 months will be compared with established local norms. Ethics and dissemination This study has ethical approval by the Ethics Committee of the Faculty of Tropical Medicine, Mahidol University (FTM ECF-019-06), Johns Hopkins University (IRB no: 00007432), Chiang Mai University (FAM-2559-04227), Oxford Tropical Research Ethics Committee (OxTREC Reference: 49-16) and by the local Tak Community Advisory Board (TCAB-02/REV/2016). The article will be published as an open-access publication.
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页数:8
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