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Prevalence of chronic hepatitis B virus infection after implementation of a hepatitis B vaccination program among children in three provinces in Cambodia
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9 13 2013
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Source: Vaccine. 31(40):4459-4464
Details:
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Alternative Title:Vaccine
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Personal Author:
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Description:Background
Hepatitis B virus (HBV) is highly endemic in Cambodia with an estimated pre-vaccine hepatitis B surface antigen (HBsAg) prevalence of 9%. By 2005, a hepatitis B vaccination program was implemented to decrease infection rates in children. We conducted a serosurvey to evaluate the impact of the vaccination program in 2011.
Methods
A cross-sectional two-stage cluster survey was conducted to estimate HBsAg prevalence among children born from 2006 to 2007 in three provinces: Phnom Penh (urban), Kratie (rural), and Ratanakiri (remote). Demographic data, as well as written or oral vaccination history were collected. Children were tested for HBsAg. Factors associated with undervaccination and HBsAg positivity were modeled.
Results
Coverage of timely hepatitis B vaccine birth dose (administered at ≤24 hours) was 55% in Phnom Penh, 36% in Kratie, and 22% in Ratanakiri. Coverage with ≥3 hepatitis B vaccine doses (HepB3) was 91% in Phnom Penh, 82% in Kratie, and 64% in Ratanakiri. When compared with children who were born in health facilities with a skilled birth attendant (SBA), children born at home without a SBA were more likely not to have received a timely BD (adjusted relative risk [aRR]=1.94; 95% CI=1.75–2.15) as were children born at home with an SBA (aRR=1.54; 95% CI=1.32–1.80). The proportion of children who tested positive for HBsAg was 0.33% in Phnom Penh, 1.41% in Kratie, and 3.45% in Ratanakiri. In all three provinces, children who received their first dose after seven days of life and children who never received hepatitis B vaccine had the highest HBsAg prevalence.
Conclusions
Progress has been made in Cambodia in decreasing the burden of chronic HBV infection among children. Improvements in vaccination coverage will further decrease the burden disease.
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Source:
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Pubmed ID:23684825
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Pubmed Central ID:PMC4663664
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Volume:31
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Issue:40
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