Elsevier

Vaccine

Volume 28, Issue 50, 23 November 2010, Pages 7947-7955
Vaccine

Serologic testing to verify the immune status of internationally adopted children against vaccine preventable diseases

https://doi.org/10.1016/j.vaccine.2010.09.069Get rights and content

Abstract

Definitive immunization guidelines for internationally adopted children are lacking. We examined whether these children had serologic evidence of protection against vaccine-preventable diseases. For children with ≥3 vaccine doses, overall protection was high for diphtheria (85%), tetanus (95%), polio (93%), hepatitis B (77%), and Hib (67%). For children ≥12 months of age with ≥1 dose of measles, mumps, or rubella vaccines, 95%, 72%, and 94% were immune, respectively. Children without immunization documentation had lower immunity. Serologic testing was useful in verifying the immunization status in internationally adopted children with and without documentation of immunizations.

Introduction

In 2008, 17,443 children were internationally adopted by families in the United States (US) and more than 200,000 children were adopted in the past decade [1]. The American Academy of Pediatrics (AAP) recommends that children undergo a comprehensive health assessment shortly after arrival to the US, including an assessment of previously administered vaccines [2]. While the Advisory Committee on Immunization Practices (ACIP) [3], the Infectious Disease Society of America (IDSA) [4], and the AAP [2] provide several options for assuring that internationally adopted children are properly immunized, no clear consensus exists about which strategy is optimal. Written records may be accepted as valid if: the vaccines, dates of administration, numbers of doses, intervals between doses, and patient's age at the time of immunization are all consistent with the current US or World Health Organization schedule. Serologic testing may also be used to verify the child's immunizations. Another option provided is to give one dose of vaccine and do serologic testing one month later. If there are concerns about whether vaccines were administered properly or were immunogenic, repeat administration of immunizations is recommended.

The lack of definitive recommendations for immunization decisions in internationally adopted children is likely due to the varied results from previously published studies [5], [6], [7], [8], [9], [10], [11], [12], [13], [14], [15]. The interpretation and comparison of results from these studies may differ due to differences in laboratory methods and definitions of protection. In addition, many of these studies have small sample sizes, minimal country-specific data, and evaluated only a few vaccine antigens. Serologic testing has been used in research settings in vaccine development and post-licensure surveillance to verify response to vaccine antigens and to provide a surrogate for protection [16]. In addition, many health care providers, employers, and public health agencies utilize serology in populations such as military recruits, health care workers, and pregnant women to document their immune status and to determine their potential need for immunization [3], [4]. Since serum antibody testing is widely accepted as a method to verify immunity [3], [4], [16], we have routinely used serologic testing to guide our recommendations for immunization in internationally adopted children. To assist in providing data for evidence-based guidelines, the objective of our study was to determine whether internationally adopted children had serologic evidence of protection against vaccine preventable diseases and to determine if documentation of immunization was associated with protective antibody levels.

Section snippets

Study population

Children evaluated at the International Adoption Center at Cincinnati Children's Hospital Medical Center (CCHMC) in Cincinnati, OH from November 1999 through June 2004 were eligible for the study if they had serologic testing for any vaccine antigen. They were excluded from the analysis for a specific antigen if they received a vaccine in the US for that antigen prior to serologic testing. In the case of hepatitis B virus (HBV), they were also excluded if they had serologic evidence of past or

Study population characteristics

Overall, 816 children were evaluated at the International Adoption Center at CCHMC from November 1999 through June 2004. After all exclusion criteria were applied, 746 remained eligible. For the HBV analysis, 31 were ineligible due to current (n = 5) or resolved infection (n = 26). Table 1 summarizes the demographic characteristics of the children studied. Consistent with US trends in international adoption [1], the majority of children emigrated from one of five countries: Russia (34%), China

Discussion

This large comprehensive study with country-specific data examined protective antibody levels to vaccine antigens to determine whether internationally adopted children had serologic evidence of protection against vaccine preventable diseases and to determine if documentation of immunization was associated with protective antibody levels. Table 4 summarizes previously published studies examining immunization verification in internationally adopted children (5–15). The countries evaluated, ages

Conclusions

In our study, the vast majority of internationally adopted children had serological evidence of protective antibodies to most vaccine antigens. Our country-specific data indicate that in children with immunization documentation, most had protective antibody levels. Therefore neither re-immunization nor serologic testing is needed, the record can be accepted as valid and the immunization series should be completed as appropriate for the child's age. Our study results provide additional data for

Acknowledgements

Salary support to Dr. Stadler during this research was provided by Molecular Epidemiology Child Environmental Health NIEHS training grant 5-T32-ES010957-08, through the Department of Environmental Health, Division of Biostatistics and Epidemiology, University of Cincinnati College of Medicine. Dr. Trehan is partly supported by NIH training grant 5-T32-HD049338-03.

We thank Jareen Meinzen-Derr, PhD and Paul Succop, PhD for their assistance with the study. We thank Dee Daniels, Linda Jamison,

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    Portions of this work were presented at the Pediatric Academic Societies’ Annual Meeting on May 17, 2005, in Washington, DC.

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