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Elimination of Mother-to-Infant Transmission of Hepatitis B Virus: 35 Years of Experience
Chronic hepatitis B viral (HBV) infection remains a major health threat, especially in high-prevalence areas. Most infants infected by mother-to-infant HBV transmission become chronic carriers. In Taiwan, many important preventive interventions have been implemented to block the perinatal transmissi...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7354867/ https://www.ncbi.nlm.nih.gov/pubmed/32704492 http://dx.doi.org/10.5223/pghn.2020.23.4.311 |
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author | Lu, Fang-Ting Ni, Yen-Hsuan |
author_facet | Lu, Fang-Ting Ni, Yen-Hsuan |
author_sort | Lu, Fang-Ting |
collection | PubMed |
description | Chronic hepatitis B viral (HBV) infection remains a major health threat, especially in high-prevalence areas. Most infants infected by mother-to-infant HBV transmission become chronic carriers. In Taiwan, many important preventive interventions have been implemented to block the perinatal transmission of HBV in the past 35 years. The first nationwide universal HBV vaccination program was launched in Taiwan in July 1984. The three-dose HBV vaccine completion rate reached 98.1% in 2018. The prevalence of Hepatitis B surface antigen (HBsAg) decreased from 9.8% in pre-vaccinated period in 1984 to 0.5% in the vaccinated cohort in 2014. The incidence of hepatocellular carcinoma in children aged 6–9 years significantly declined from 0.52 to 0.13 per 100,000 children born before and after 1984, respectively. Furthermore, we have performed a maternal HBV screening program during pregnancy since 1984, with the screening rate peaked at 93% in 2012. The HBsAg- and HBeAg-seropositive rate in pregnant women declined from 13.4% and 6.4% in 1984–1985 to 5.9% and 1.0% in 2016, respectively. To closely control perinatal HBV infection, we have administered hepatitis B immunoglobulin immediately after birth and checked the serum level of HBsAg and anti-HBs in high-risk babies born to HBsAg-seropositive mothers, irrespective of their HBeAg status, since July 2019. We have also adopted short-term antiviral treatments such as tenofovir 300 mg daily in the third trimester for highly viremic mothers and reduced the perinatal infection rates from 10.7 to 1.5%. Through all these efforts, we expect to meet the global goal of eliminating HBV infection by 2030. |
format | Online Article Text |
id | pubmed-7354867 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition |
record_format | MEDLINE/PubMed |
spelling | pubmed-73548672020-07-22 Elimination of Mother-to-Infant Transmission of Hepatitis B Virus: 35 Years of Experience Lu, Fang-Ting Ni, Yen-Hsuan Pediatr Gastroenterol Hepatol Nutr Review Article Chronic hepatitis B viral (HBV) infection remains a major health threat, especially in high-prevalence areas. Most infants infected by mother-to-infant HBV transmission become chronic carriers. In Taiwan, many important preventive interventions have been implemented to block the perinatal transmission of HBV in the past 35 years. The first nationwide universal HBV vaccination program was launched in Taiwan in July 1984. The three-dose HBV vaccine completion rate reached 98.1% in 2018. The prevalence of Hepatitis B surface antigen (HBsAg) decreased from 9.8% in pre-vaccinated period in 1984 to 0.5% in the vaccinated cohort in 2014. The incidence of hepatocellular carcinoma in children aged 6–9 years significantly declined from 0.52 to 0.13 per 100,000 children born before and after 1984, respectively. Furthermore, we have performed a maternal HBV screening program during pregnancy since 1984, with the screening rate peaked at 93% in 2012. The HBsAg- and HBeAg-seropositive rate in pregnant women declined from 13.4% and 6.4% in 1984–1985 to 5.9% and 1.0% in 2016, respectively. To closely control perinatal HBV infection, we have administered hepatitis B immunoglobulin immediately after birth and checked the serum level of HBsAg and anti-HBs in high-risk babies born to HBsAg-seropositive mothers, irrespective of their HBeAg status, since July 2019. We have also adopted short-term antiviral treatments such as tenofovir 300 mg daily in the third trimester for highly viremic mothers and reduced the perinatal infection rates from 10.7 to 1.5%. Through all these efforts, we expect to meet the global goal of eliminating HBV infection by 2030. The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition 2020-07 2020-07-03 /pmc/articles/PMC7354867/ /pubmed/32704492 http://dx.doi.org/10.5223/pghn.2020.23.4.311 Text en Copyright © 2020 by The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition https://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Lu, Fang-Ting Ni, Yen-Hsuan Elimination of Mother-to-Infant Transmission of Hepatitis B Virus: 35 Years of Experience |
title | Elimination of Mother-to-Infant Transmission of Hepatitis B Virus: 35 Years of Experience |
title_full | Elimination of Mother-to-Infant Transmission of Hepatitis B Virus: 35 Years of Experience |
title_fullStr | Elimination of Mother-to-Infant Transmission of Hepatitis B Virus: 35 Years of Experience |
title_full_unstemmed | Elimination of Mother-to-Infant Transmission of Hepatitis B Virus: 35 Years of Experience |
title_short | Elimination of Mother-to-Infant Transmission of Hepatitis B Virus: 35 Years of Experience |
title_sort | elimination of mother-to-infant transmission of hepatitis b virus: 35 years of experience |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7354867/ https://www.ncbi.nlm.nih.gov/pubmed/32704492 http://dx.doi.org/10.5223/pghn.2020.23.4.311 |
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