Abstract
BackgroundIn 1999, the American Academy of Pediatrics and U.S. Public Health Service recommended suspending the birth dose of hepatitis B vaccine due to concerns about potential mercury exposure. A previous report found that overall national hepatitis B vaccination coverage rates decreased in association with the suspension. It is unknown whether this underimmunization occurred uniformly or was associated with how providers changed their practices for the timing of hepatitis B vaccine doses. We evaluate the impact of the birth dose suspension on underimmunization for the hepatitis B vaccine series among 24-month-olds in five large provider groups and describe provider practices potentially associated with underimmunization following the suspension.MethodsRetrospective cohort study of children enrolled in five large provider groups in the United States (A-E). Logistic regression was used to evaluate the association between the birth dose suspension and a child's probability of being underimmunized at 24 months for the hepatitis B vaccine series.ResultsPrior to July 1999, the percent of children who received a hepatitis B vaccination at birth varied widely (3% to 90%) across the five provider groups. After the national recommendation to suspend the hepatitis B birth dose, the percent of children who received a hepatitis B vaccination at birth decreased in all provider groups, and this trend persisted after the policy was reversed. The most substantial decreases were observed in the two provider groups that shifted the first hepatitis B dose from birth to 5–6 months of age. Accounting for temporal trend, children in these two provider groups were significantly more likely to be underimmunized for the hepatitis B series at 24 months of age if they were in the birth dose suspension cohort compared with baseline (Group D OR 2.7, 95% CI 1.7 – 4.4; Group E OR 3.1, 95% CI 2.3 – 4.2). This represented 6% more children in Group D and 9% more children in Group E who were underimmunized in the suspension cohort compared with baseline. Children in the reversal cohort in these groups remained significantly more likely to be underimmunized compared with baseline. In contrast, in a third provider group where the typical timing of the third dose was unchanged and in two other provider groups whose hepatitis B vaccination schedules were unaffected by the birth dose suspension, hepatitis B vaccination coverage either was maintained or improved.ConclusionWhen the hepatitis B birth dose was suspended, provider groups that moved the first dose of vaccination to 5–6 months of age or later had decreases in hepatitis B vaccine coverage at 24 months. These findings suggest that as vaccine policy changes occur, providers could attempt to minimize underimmunization by adopting vaccination schedules that minimize delays in the recommended timing of vaccine doses.
Highlights
In 1999, the American Academy of Pediatrics and U.S Public Health Service recommended suspending the birth dose of hepatitis B vaccine due to concerns about potential mercury exposure
While information was limited regarding the potential adverse effects of exposure through childhood vaccination to thimerosal, a preservative in vaccines that is metabolized into ethylmercury, [1,2] the American Academy of Pediatrics (AAP) and the United States Public Health Service (US PHS) issued a Joint Statement in July 1999 to describe several key actions intended to assure the replacement of thimerosal-containing vaccines with thimerosal-free formulations while encouraging the maintenance of childhood vaccination coverage levels[3]
After the birth dose suspension, children in all five provider groups were less likely to receive a hepatitis B birth dose, with children in Group D and Group E experiencing substantial declines that persisted even after reversal of the suspension recommendations
Summary
In 1999, the American Academy of Pediatrics and U.S Public Health Service recommended suspending the birth dose of hepatitis B vaccine due to concerns about potential mercury exposure. While information was limited regarding the potential adverse effects of exposure through childhood vaccination to thimerosal, a preservative in vaccines that is metabolized into ethylmercury, [1,2] the American Academy of Pediatrics (AAP) and the United States Public Health Service (US PHS) issued a Joint Statement in July 1999 to describe several key actions intended to assure the replacement of thimerosal-containing vaccines with thimerosal-free formulations while encouraging the maintenance of childhood vaccination coverage levels[3] In this Statement, they recommended as an additional precaution the temporary deferment of the first dose of hepatitis B vaccine until 2–6 months of age for infants born to hepatitis B surface antigen-negative women. A disruption in hepatitis B vaccination coverage following the birth dose suspension was observed in a nationally representative sample of 19month olds[9]
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