scholarly journals 1055. Assessing the Impact of the Routine Childhood Hepatitis B Immunization and the Need for Hepatitis B Vaccine Birth Dose in Sierra Leone, 2018

2020 ◽  
Vol 7 (Supplement_1) ◽  
pp. S557-S557
Author(s):  
Lucy Breakwell ◽  
Dennis Marke ◽  
Reinhard Kaiser ◽  
Alexandra Tejada-Strop ◽  
Matthew Pauly ◽  
...  

Abstract Background All African countries recommend 3 doses of hepatitis B vaccine (HepB3), most at 6, 10, and 14 weeks of age, but few recommend a HepB birth dose (HepB-BD). To evaluate the role of mother to child transmission (MTCT) of hepatitis B virus (HBV) with the 3 dose HepB schedule, we conducted a serosurvey in Sierra Leone among 4–30 month old children and their mothers, and 5–9 year old children. Methods We conducted a multi-stage cluster survey in 3 districts. Enumeration areas (EA) were selected by probability proportional to size, followed by random selection of eligible households to identify 1901 children per age group. We tested all participants for HBV surface antigen (HBsAg) by rapid test and collected children’s HepB vaccination history. Serum from all HBsAg+ mothers and 1 HBsAg- mother per EA was tested for total antibodies to HBV core antigen (anti-HBc), HBsAg, HBV e antigen (HBeAg), and HBV DNA. We assessed the association of HBsAg prevalence with HepB vaccination and maternal HBV markers. Results Among 1889 children aged 4–30 months, 20 (1.3%; 95% CI:0.8%–2.0%) were HBsAg+; HepB3 coverage was 85%. Among 2025 children aged 5–9 years, 32 (1.6%; 95% CI:1.1%–2.3%) were HBsAg+; HepB3 coverage was 77%. Of HBsAg+ children, 70% (14/20) of younger and 56% (18/32) of older children received HepB3. Among 1776 mothers of younger children, 169 (9.8%; 95% CI:8.1%–11.7%) were HBsAg+. HBsAg prevalence for children with HBsAg+ mothers was 5.9% (10/169) and 0.7% (6/1605) for those with HBsAg- mothers (adjusted OR=10.6 [95% CI:2.8–40.8]). Of 139 HBsAg+ mothers, 13 (9%) were HBeAg+ and 126 (91%) had detectable HBV DNA. Maternal HBsAg (p=0.026), HBeAg (p< 0.001), and HBV DNA levels ≥ 200,000 IU/mL (p< 0.001) were associated with HBsAg positivity in younger children (Table 1). Table 1: Association of maternal HBV serological and molecular markers with HBsAg positivity in 4–30-month old children — Sierra Leone hepatitis B serosurvey, 2018 Conclusion HBsAg prevalence was much lower among children than among mothers, for whom HepB would not have been available, indicating that routine infant HepB vaccination has substantially lowered HBV burden. Increasing HepB3 coverage could further reduce HBsAg prevalence among children. As HBsAg positivity in young children was strongly associated with having a mother with active HBV infection and > 50% of HBsAg+ children received HepB3, HepB-BD is needed to prevent MTCT of HBV and chronic HBV infections in children. Disclosures All Authors: No reported disclosures

Author(s):  
Hongyu Huang ◽  
Chenyu Xu ◽  
Lanhua Liu ◽  
Liping Chen ◽  
Xiaoqin Zhu ◽  
...  

Abstract Background Passive-active immunoprophylaxis against mother-to-child transmission (MTCT) of hepatitis B virus (HBV) recommends administering hepatitis B immunoglobulin (HBIG) and birth-dose hepatitis B vaccine in infants within 12 or 24 hours after birth. With this protocol, MTCT of HBV still occurs in 5–10% infants of HBV-infected mothers with positive hepatitis B e antigen (HBeAg). The present study aimed to investigate whether earlier administration of HBIG and hepatitis B vaccine after birth can further increase protection efficacy. Methods We conducted a prospective, multi-center observational study in infants born to mothers with HBV infection, in whom neonatal HBIG and birth dose hepatitis B vaccine were administered within one hour after birth. The infants were followed up for HBV markers at 7–14 months of age. Results A total of 1140 pregnant women with HBV were enrolled, and 982 infants (9 twins) of 973 mothers were followed up at 9.6 ± 1.9 months of age. HBIG and birth-dose vaccine were administered in newborn infants within a median of 0.17 (0.02–1.0) hours after birth. The overall rate of MTCT was 0.9% (9/982), with none (0%) of the 607 infants of HBeAg-negative mothers and 9 (2.4%) of 375 infants of HBeAg-positive mothers acquiring HBV. All 9 HBV-infected infants were born to mothers with HBV DNA >2.75 × 106 IU/mL. Maternal HBV DNA levels >2 × 106 IU/mL were an independent risk factor (odds ratio, 10.627; 95% confidence interval, 2.135–∞) for immunoprophylaxis failure. Conclusions Earlier use (within 1 hour after birth) of HBIG and hepatitis B vaccine can provide better protection efficacy against MTCT of HBV.


1998 ◽  
Vol 26 (4) ◽  
pp. 895-897 ◽  
Author(s):  
A. Eduardo Silva ◽  
Brian J. McMahon ◽  
Alan J. Parkinson ◽  
Maria H. Sjogren ◽  
Jay H. Hoofnagle ◽  
...  

Vaccine ◽  
2018 ◽  
Vol 36 (27) ◽  
pp. 3901-3907 ◽  
Author(s):  
Xiaoli Liu ◽  
Chenlu Yang ◽  
Qiuyue Zhong ◽  
Qiying Song ◽  
Xiaona Huang ◽  
...  

2021 ◽  
Vol 30 (4) ◽  
pp. 86-92
Author(s):  
Vu Hai Ha ◽  
Dao Trung Nguyen ◽  
Ngo Thi Thanh Van ◽  
Pham Dinh Long ◽  
Pham Quang Thai

A cross-sectional study in 63 provinces/cities in Vietnam (2014-2018) was conducted to describe the coverage of hepatitis B vaccine birth dose from 2014-2018 in Vietnam. The results showed that the coverage proportion of Hepatitis B vaccine birth dose (hepB-BD) in Vietnam during 2014-2018 was 73.4%, of which the proportion of hepB-BD with in 24 hours and after 24 hours of births were 68.7% and 4.7%, respectively. There was diffirent between socio-economic areas (p<0.01). The proportions of hepB-BD in Mekong River Delta area and in Northern midlands and mountain area were highest (81.7%) and lowest (57.2%), respectively. The coverage proportion of hepB-BD in Vietnam during 2014-2018 was low, varied unevenly between years and regions/areas. Enhancing the coverage of hepB-BD, especially hepB-BD vaccination within 24 hours of births will be highly recommended.


Vaccine ◽  
2020 ◽  
Vol 38 (52) ◽  
pp. 8343-8350
Author(s):  
Xuan Thanh Thi Le ◽  
Atsuyoshi Ishizumi ◽  
Huong Thi Thu Nguyen ◽  
Hong Thi Duong ◽  
Huyen Thi Thanh Dang ◽  
...  

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