Efficacy and safety of lamivudine treatment in late pregnancy with high HBV DNA: a perspective for mother and infants.

INTRODUCTION Perinatal transmission - from mother to fetus - is one of the main transmission routes of chronic hepatitis B (CHB) infection. Lamivudine therapy has been reported to prevent the replication of hepatitis B virus (HBV) in pregnant women with a high viral load that can lead to perinatal transmission. METHODOLOGY This study sought to evaluate retrospectively the efficacy and safety of lamivudine treatment in pregnant women with CHB and a high viral load. Biochemical parameters, and virological and serological responses at the 32nd and 36th week of gestation and after labor were recorded. The complications of CHB and the adverse effects of lamivudine treatment were also recorded. RESULTS Following 8 weeks of lamivudine treatment, HBV viral load decreased to levels ≤ 10,000 copies/ml in five of the seven patients (71%) and in three patients (43%), HBV DNA was found to be completely negative after labor. Neither adverse effects caused by lamivudine treatment nor complications due to CHB infection were experienced by mothers or infants. CONCLUSIONS The results of this study suggest that lamivudine therapy in highly viremic hepatitis B surface antigen (HBsAg)-positive pregnant women could decrease perinatal transmission rates of HBV, and can lower the HBV viral load during labor.

[1]  O. Halıcıoğlu,et al.  Lamivudine and adefovir resistance in children and young adults with chronic hepatitis B. , 2010, International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases.

[2]  Hung‐Chih Yang,et al.  Lamivudine in late pregnancy to prevent perinatal transmission of hepatitis B virus infection: a multicentre, randomized, double‐blind, placebo‐controlled study , 2009, Journal of viral hepatitis.

[3]  W. Kremers,et al.  Pregnancy-associated acute liver disease and acute viral hepatitis: differentiation, course and outcome. , 2008, Journal of hepatology.

[4]  Jeng-Hsiu Hung,et al.  Lamivudine therapy in the treatment of chronic hepatitis B with acute exacerbation during pregnancy. , 2008, Journal of the Chinese Medical Association : JCMA.

[5]  Xiao-wei Xu,et al.  Current therapy with nucleoside/nucleotide analogs for patients with chronic hepatitis B. , 2006, Hepatobiliary & pancreatic diseases international : HBPD INT.

[6]  K. Pan,et al.  Efficacy and safety of lamivudine treatment for chronic hepatitis B in pregnancy. , 2004, World journal of gastroenterology.

[7]  H. Janssen,et al.  Lamivudine treatment during pregnancy to prevent perinatal transmission of hepatitis B virus infection , 2003, Journal of viral hepatitis.

[8]  D. Cui,et al.  [Analysis of fetal distress in pregnancy with hepatitis B virus infection]. , 2002, Zhonghua fu chan ke za zhi.

[9]  P. Madelenat,et al.  Prise en charge des femmes enceintes infectées par le VIH à l’hôpital Bichat entre 1990 et 1998 : analyse de 202 grossesses , 2001 .

[10]  P. Faucher,et al.  [Management of pregnant women infected with HIV at Bichat Hospital between 1990 and 1998: analysis of 202 pregnancies]. , 2001, Gynecologie, obstetrique & fertilite.

[11]  H. Niesters,et al.  Letters to the Editor: Lamivudine in the last 4 weeks of pregnancy to prevent perinatal transmission in highly viremic chronic hepatitis B patients , 2000 .

[12]  R. D. de Man,et al.  Lamivudine in the last 4 weeks of pregnancy to prevent perinatal transmission in highly viremic chronic hepatitis B patients. , 2000, Journal of hepatology.

[13]  G. E. Pakes,et al.  Clinical Pharmacokinetics of Lamivudine , 1999, Clinical pharmacokinetics.

[14]  P. Harrigan,et al.  Pharmacokinetics and antiretroviral activity of lamivudine alone or when coadministered with zidovudine in human immunodeficiency virus type 1-infected pregnant women and their offspring. , 1998, The Journal of infectious diseases.

[15]  W. Fetter,et al.  Ten-year neonatal hepatitis B vaccination program, The Netherlands, 1982-1992: protective efficacy and long-term immunogenicity. , 1997, Vaccine.

[16]  Health Organization Hepatitis B and breastfeeding. , 1997, Indian Pediatrics.

[17]  H. Reesink,et al.  PREVENTION OF HEPATITIS B VIRUS CARRIER STATE IN INFANTS ACCORDING TO MATERNAL SERUM LEVELS OF HBV DNA , 1989, The Lancet.

[18]  S. Krugman,et al.  Perinatal hepatitis B virus transmission in the United States. Prevention by passive-active immunization. , 1985 .

[19]  Seeff Lb,et al.  Passive and active immunoprophylaxis of hepatitis B. , 1984 .

[20]  L. Seeff,et al.  Passive and active immunoprophylaxis of hepatitis B. , 1984, Gastroenterology.

[21]  M. Imai,et al.  e antigen and anti-e in the serum of asymptomatic carrier mothers as indicators of positive and negative transmission of hepatitis B virus to their infants. , 1976, The New England journal of medicine.

[22]  R. Beasley,et al.  Vertical transmission of hepatitis B antigen in Taiwan. , 1975, The New England journal of medicine.