Perinatal transmission of hepatitis B virus: an Australian experience

被引:276
作者
Wiseman, Elke [1 ]
Fraser, Melissa A. [1 ]
Holden, Sally [2 ]
Glass, Anne [1 ]
Kidson, Bronwynne L. [1 ]
Heron, Leon G. [3 ]
Maley, Michael W. [4 ]
Ayres, Anna [5 ]
Locarnini, Stephen A. [5 ]
Levy, Miriam T. [1 ]
机构
[1] Liverpool Hosp, Sydney SW Area Hlth Serv, Sydney, NSW, Australia
[2] Univ New S Wales, Sydney, NSW, Australia
[3] Childrens Hosp Westmead, Natl Ctr Immunisat Res & Surveillance Vaccine Pre, Sydney, NSW, Australia
[4] Sydney SW Pathol Serv, Sydney, NSW, Australia
[5] Victorian Infect Dis Reference Lab, Melbourne, Vic, Australia
关键词
FAILED POSTNATAL IMMUNOPROPHYLAXIS; IMMUNOGLOBULIN; INTERRUPTION; PREVENTION; BABIES;
D O I
10.5694/j.1326-5377.2009.tb02524.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To determine the rate of perinatal hepatitis B virus (HBV) transmission in an Australian setting and to identify maternal virological factors associated with highest risk of transmission. Design, participants and setting: A prospective, observational study of perinatal transmission of HBV Participants were pregnant women attending Sydney South West Area Health Service antenatal clinics who tested positive for hepatitis B surface antigen (HBsAg), and their babies. All babies were routinely offered hepatitis B immunoglobulin (HBIG) and HBV vaccination. Babies positive for HBsAg at 9-month follow-up underwent further virological testing, including HBV DNA sequencing. The study was conducted between August 2002 and May 2008. Main outcome measures: HBV DNA levels and demographic characteristics of HBsAg-positive pregnant women; proportion of their infants with active HBV infection at 9-month follow-up; maternal characteristics affecting transmission rate; HBV DNA sequencing of infected infants and their mothers. Results: Of 313 HBsAg-positive pregnant women, 213 (68%) were HBV DNA-positive and 92 (29%) were positive for hepatitis B "e" antigen (HBeAg); 138 babies born to HBV DNA-positive mothers were tested for HBV infection (HBsAg positivity) at about 9 months of age. Four cases of transmission were identified. All four mothers had very high HBV DNA levels (> 10(8) copies/mL) and were HBeAg-positive. Three of the four infants were infected with wild-type HBV strains, with identical maternal/infant isolates. The fourth mother-infant pair had an S gene variant, HBV D144E, which has been previously reported in association with vaccine/HBIG escape. (Unfortunately, HBIG was inadvertently omitted from the immunisation schedule of this infant.) Transmission rates were 4/138 (3%) from HBV DNA-positive mothers overall, 4/61 (7%) from HBeAg-positive mothers, and 4/47 (9%) from mothers with very high HBV DNA levels. No transmission was seen in 91 babies of mothers with HBV DNA levels < 10(8) copies/mL. Conclusion: In this cohort, HBV perinatal transmission was restricted to HBeAg-positive mothers with very high viral loads.
引用
收藏
页码:489 / 492
页数:4
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