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Evaluation of the Protection Provided by Hepatitis B Vaccination in India
Jacob Puliyel1, Pathik Naik2, Ashish Puliyel3
1Department of Pediatrics, St Stephens Hospital, Delhi, 110054, India. Puliyel@gmail.com.
Insights
Hepatitis B birth dose vaccination in India offers protection against infection, but vaccination at six weeks provides similar benefits. The study supports current government recommendations for home-delivered babies.
Area of Science:
- Pediatrics
- Immunology
- Public Health
Background:
- Hepatitis B vaccination in India is typically recommended at six weeks of age, with exceptions for hospital deliveries.
- The study investigates the protective efficacy of the Hepatitis B birth dose in Indian children.
Purpose of the Study:
- To evaluate the effectiveness of the Hepatitis B birth dose in preventing Hepatitis B virus (HBV) infection.
- To compare the protection offered by a birth dose versus vaccination at six weeks of age.
Main Methods:
- A case-control study involving 2671 children aged 1 to 5 years.
- Testing for Hepatitis B surface antigen (HBsAg), Hepatitis B core antibody (HBcAb), and Hepatitis B surface antibody (HBsAb).
- Recording vaccination history, with cases defined as HBsAg carriers or infected children (HBsAg and/or HBcAb positive).
Main Results:
- Birth dose vaccination showed an odds ratio (OR) of 0.35 for HBsAg positivity compared to unvaccinated children.
- Vaccination at six weeks had an OR of 0.29 for HBsAg positivity.
- The birth dose demonstrated an OR of 0.42 for HBV infection, while vaccination at six weeks had an OR of 0.49 compared to unvaccinated.
- Approximately 70% of vaccinated children had protective antibodies (HBsAb).
Conclusions:
- The study supports the Indian government's policy of vaccinating babies born at home starting at six weeks.
- While the birth dose offers protection, vaccination at six weeks appears to provide comparable benefits.
Objective:
In India, Hepatitis B vaccination is recommended at 6 wk except for hospital-deliveries. The authors examined protection afforded by the birth dose.
Methods:
A case-control study was done. HBsAg and HBcAb were tested in 2671 children, 1 to 5 y and HBsAb was evaluated in a subset of 1413 children. Vaccination history was recorded. Cases were HBsAg carriers. In another analysis, children who got infected (HBsAg and/or HBcAb positive) were considered as cases. Exposed were the unvaccinated. In another analysis, exposed were those vaccinated without the birth dose.
Results:
The odds ratio (OR) for HBsAg positivity with birth vaccination was 0.35 (95% CI 0.19-0.66); while with vaccination at 6 wk was 0.29 (95%CI 0.14-0.61), both compared to unvaccinated. Birth vaccination has no added protection when compared to the unvaccinated. Unvaccinated children in index study had HBsAg positivity of 4.38%. The number needed to treat (NNT) to prevent one case of HBsAg positivity was 32.6 (95% CI, 20.9 to 73.6). The odds of getting HBV infection was 0.42 (CI 0.25-0.68) with birth dose and 0.49 (CI 0.30-0.82) without the birth dose compared to the unvaccinated. Protective antibody (HBsAb) was present in about 70% of the vaccinated. In the unimmunised, in the first 2 y HBsAb protection was present in 40%. The odds ratio (OR) for HBsAb in the fully vaccinated between 4 and 5 y was 1.4 (95%CI 0.9-2.18) compared to the unvaccinated.
Conclusions:
The present study lends support to the pragmatic approach of the Government to vaccinate babies born at home starting at 6 wk.
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