Antiviral therapy for hepatitis B virus during second pregnancies

被引:8
|
作者
Wakano, Yasuhiro [1 ]
Sugiura, Tokio [1 ]
Endo, Takeshi [1 ]
Ito, Koichi [1 ]
Suzuki, Mitsuyoshi [4 ]
Tajiri, Hitoshi [5 ]
Tanaka, Yasuhito [2 ,3 ]
Saitoh, Shinji [1 ]
机构
[1] Nagoya City Univ, Grad Sch Med Sci, Dept Pediat & Neonatol, Nagoya, Aichi, Japan
[2] Nagoya City Univ, Grad Sch Med Sci, Dept Virol, Nagoya, Aichi, Japan
[3] Nagoya City Univ, Grad Sch Med Sci, Liver Unit, Nagoya, Aichi, Japan
[4] Juntendo Univ, Dept Pediat, Grad Sch Med, Tokyo, Japan
[5] Osaka Gen Med Ctr, Dept Pediat, Osaka, Japan
关键词
hepatitis B virus; lamivudine; mother-to-child transmission; pregnancy; tenofovir; TENOFOVIR DISOPROXIL FUMARATE; TO-INFANT TRANSMISSION; PERINATAL TRANSMISSION; VIRAL LOAD; MOTHER; LAMIVUDINE; INFECTION; EFFICACY; SAFETY; PREVENTION;
D O I
10.1111/jog.13540
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Mother-to-child transmission of the hepatitis B virus (HBV) is a major concern for infected mothers, especially after their first child has become an HBV carrier despite immunoprophylaxis. Eight mothers whose first child had become an HBV carrier despite immunoprophylaxis were referred for antiviral therapy during the subsequent pregnancy. All pregnant women were seropositive for both the hepatitis B surface antigen and hepatitis B e antigen. In the treatment group (three receiving lamivudine and two receiving tenofovir), mother-to-child transmission of the HBV was successfully prevented in all infants (5/5). On the other hand, two of three infants became HBV carriers in the untreated group. There were no significant adverse effects in either mothers or infants. Antiviral therapy using lamivudine and tenofovir during the second pregnancy successfully prevented mother-to-child transmission of the HBV for high-risk mothers.
引用
收藏
页码:566 / 569
页数:4
相关论文
共 50 条
  • [1] Modeling Complex Decay Profiles of Hepatitis B Virus During Antiviral Therapy
    Dahari, Harel
    Shudo, Emi
    Ribeiro, Ruy M.
    Perelson, Alan S.
    [J]. HEPATOLOGY, 2009, 49 (01) : 32 - 38
  • [2] Hepatitis B virus mutations associated with antiviral therapy
    Bartholomeusz, A.
    Locarnini, S.
    [J]. JOURNAL OF MEDICAL VIROLOGY, 2006, 78 : S52 - S55
  • [3] Hepatitis B virus genotypes and response to antiviral therapy
    Enomoto, M
    Tamori, A
    Nishiguchi, S
    [J]. CLINICAL LABORATORY, 2006, 52 (1-2) : 43 - 47
  • [4] Antiviral therapy and resistance with hepatitis B virus infection
    Hans L Tillmann
    [J]. World Journal of Gastroenterology, 2007, (01) : 125 - 140
  • [5] Antiviral therapy and resistance with hepatitis B virus infection
    Tillmann, Hans L.
    [J]. WORLD JOURNAL OF GASTROENTEROLOGY, 2007, 13 (01) : 125 - 140
  • [6] Hepatic flare after telbivudine withdrawal and efficacy of postpartum antiviral therapy for pregnancies with chronic hepatitis B virus
    Liu, Jinfeng
    Wang, Jing
    Jin, Dongfang
    Qi, Caijing
    Yan, TaoTao
    Cao, Furong
    Jin, Li
    Tian, Zhen
    Guo, Dandan
    Yuan, Ningxia
    Feng, Weihong
    Zhang, Shulin
    Zhao, Yingren
    Chen, Tianyan
    [J]. JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2017, 32 (01) : 177 - 183
  • [7] Hepatic Decompensation during Hepatitis B antiviral Therapy
    Klein, Friederike
    [J]. ZEITSCHRIFT FUR GASTROENTEROLOGIE, 2021, 59 (12): : 1262 - 1262
  • [8] Monitoring During and After Antiviral Therapy for Hepatitis B
    Andersson, Karin L.
    Chung, Raymond T.
    [J]. HEPATOLOGY, 2009, 49 (05) : S166 - S173
  • [9] Antiviral therapy for hepatitis B virus associated hepatic failure
    Yu-Ming Wang and Ying-Zi Tang Institute for Infectious Diseases of PLA
    [J]. Hepatobiliary & Pancreatic Diseases International, 2009, 8 (01) : 17 - 24
  • [10] Genetic variability of hepatitis B virus and response to antiviral therapy
    Liu, Chun-Jen
    Kao, Jia-Horng
    [J]. ANTIVIRAL THERAPY, 2008, 13 (05) : 613 - 624