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Persons using assistive technology might not be able to fully access information in this file. For assistance, please send e-mail to: mmwrq@cdc.gov. Type 508 Accommodation and the title of the report in the subject line of e-mail. Hepatitis B Vaccination Coverage Among Adults --- United States, 2004Hepatitis B virus (HBV) infection is a major cause of cirrhosis and liver cancer in the United States. The Advisory Committee on Immunization Practices (ACIP) has recommended a comprehensive strategy to eliminate HBV transmission, including prevention of perinatal HBV transmission; universal vaccination of infants; catch-up vaccination of unvaccinated children and adolescents; and vaccination of unvaccinated adults at increased risk for infection. The incidence of acute hepatitis B has declined 75%, from 8.5 per 100,000 population in 1990 to 2.1 per 100,000 population in 2004, with the greatest declines (94%) among children and adolescents (1). Incidence remains highest among adults, who accounted for approximately 95% of the estimated 60,000 new infections in 2004. To measure hepatitis B vaccination coverage among adults, data were analyzed from the 2004 National Health Interview Survey (NHIS). This report summarizes the results of that analysis, which indicated that, during 2004, 34.6% of adults aged 18--49 years reported receiving hepatitis B vaccine, including 45.4% of adults at high risk for HBV infection. To accelerate elimination of HBV transmission in the United States, public health programs and clinical care providers should implement strategies to ensure that adults at high risk are offered hepatitis B vaccine. NHIS is a multipurpose household health survey of the U.S. civilian, noninstitutionalized population, conducted by in-person interview. Hepatitis B vaccination coverage was estimated from self reports of sampled adults. The analysis was restricted to adults aged 18--49 years, age groups that account for approximately 80% of adult HBV infections. In the 2004 NHIS, adults who responded "yes" to the question, "Have you ever received hepatitis B vaccine?" were assumed to have received >1 vaccine dose. For this analysis, adults were considered at high risk for HBV infection if they reported a risk factor in answering any of three questions related to human immunodeficiency virus (HIV) and sexually transmitted disease (STD) risk behaviors.* For all adults aged >18 years, weighted age-specific and national hepatitis B vaccination coverage rates were estimated. Statistical analysis software was used to calculate weighted estimates and confidence intervals. Chi-square tests were used to compare coverage rates among groups. P-values <0.05 were considered statistically significant. Coverage rates with relative standard errors >0.30 were not reported. A logistic model was developed to determine whether high risk was an independent predictor of vaccination, including as possible confounders all terms identified to be predictors of vaccination in univariate analysis and those that have been determined to be associated in other studies. The final model fit the data (Hosmer-Lemeshow goodness-of-fit, p = 0.36). During 2004, a total of 31,326 adults were interviewed, including 18,269 aged 18--49 years. The response rate was 72.5% (2). Of eligible adults aged 18--49 years, 17,249 (94%) who responded to the hepatitis B vaccination questions were included in this analysis, including 1,048 (5.7%) adults at high risk. A weighted analysis of adults who were surveyed indicated that 34.6% (95% CI = 33.5%--35.6%) reported receiving hepatitis B vaccine. Coverage was highest among persons aged 18--20 years and declined with increasing age (Table). Coverage also was higher for persons in occupations for which vaccination is specifically recommended, including health-care workers (80.5%; CI = 77.3%--83.4%) and police officers or firefighters (63.6%; CI = 56.6%--70.1%), and for adults at high risk (45.4%; CI = 41.7%--49.2%). Report of hepatitis B vaccination also was associated with certain population characteristics, including female sex, non-Hispanic ethnicity, and higher educational achievement. Persons with a routine source of health care (e.g., primary doctor, health maintenance organization, or clinic) and persons with health insurance also were more likely to report vaccination than those with no routine source of health care (Table). The same demographic and health-care use characteristics were associated with higher likelihood of vaccination among persons at high risk as among other respondents. In a multivariate model, after controlling for age, sex, education, occupation, and HIV test history, high risk remained a statistically significant predictor (adjusted odds ratio = 1.3) of hepatitis B vaccination. Reported by: C Weinbaum, MD, K Billah, PhD, EE Mast, MD, Div of Viral Hepatitis, National Center for HIV, Viral Hepatitis, STDs, and Tuberculosis Prevention (proposed), CDC. Editorial Note:The findings in this report suggest that hepatitis B vaccination coverage among adults at high risk, as measured by NHIS, has increased substantially from 30% in 2000 to 45% in 2004 (3). Some of this increase in coverage represents the aging of persons vaccinated as adolescents, reflecting the effect of ACIP recommendations for routine vaccination of adolescents that were first made in 1995 (4). In addition, higher vaccination coverage among persons of all ages at high risk suggests successes vaccinating targeted adults and likely contributed to a decline in hepatitis B incidence. From 2000 to 2004, hepatitis B incidence among adults decreased 27%, from 3.7 to 2.7 per 100,000 population (CDC, unpublished data, 2006). However, hepatitis B vaccination coverage of adults at high risk remained lower than vaccination coverage of children (92%) and adolescents (86%) in 2004 (5), two other age groups included in the ACIP vaccination strategy to eliminate HBV transmission. Several factors contribute to low hepatitis B vaccination coverage among adults at high risk. In contrast to vaccination of children, national programs that support vaccine purchase and infrastructure for vaccine administration are not available for adults. As a result, adults at increased risk often have missed opportunities to receive hepatitis B vaccination. In a study of 483 adults with acute hepatitis B infection, 61% reported a missed opportunity for vaccination during STD treatment, incarceration, or drug treatment during 2001--2004 (6). In primary care settings, patients and providers might be reluctant to discuss risk behaviors (7), and providers might not prioritize vaccination in the context of other clinical care services. Adult vaccination coverage can be increased through the use of provider reminders and other interventions to increase access to vaccination (8). Demonstration projects have determined that provision of comprehensive HIV, viral hepatitis, and STD services increases vaccination coverage (9). In October 2005, ACIP provisionally recommended strategies to improve vaccination for adults at risk for hepatitis B, emphasizing vaccination of all adults at venues where a high proportion of persons are likely to have risk factors for HBV infection (e.g., STD/HIV testing and treatment facilities, correctional facilities, and drug-abuse treatment facilities) and the adoption of practices that remove barriers to vaccination in primary care settings (10). The findings in this report are subject to at least four limitations. First, criteria for adults at high risk used in this study might not identify all persons who are at risk for HBV infection, such as persons with multiple sex partners, and might identify persons without risk, such as most persons with hemophilia. Second, the in-person format of the interview might lead to underreporting of risk behaviors. Third, hepatitis B vaccination was based on self-report and was not validated by medical records. Although differences might exist between self-reported vaccination and true vaccination, directional bias is unlikely, so correlates and trends in coverage are likely to reflect true trends. Finally, NHIS excludes all institutionalized persons (e.g., military or incarcerated) among whom both the risk for hepatitis B and vaccination coverage might differ from those of the rest of the population. Despite these limitations, NHIS is the only national survey that collects data related to adult hepatitis B vaccination. Hepatitis B vaccine is safe and effective and the only licensed vaccine that prevents cancers. Despite these benefits, the majority of adults at risk for HBV remain unvaccinated. To increase coverage, public health programs and primary care providers should inform adults receiving preventive clinical services of the potential benefits of hepatitis B vaccination for their health, vaccinate all adults who seek protection from HBV, and adopt strategies appropriate for the practice setting to ensure that all adults at risk for HBV infection are offered hepatitis B vaccine. Acknowledgments This report is based, in part, on data contributed by S Stokley, MPH, National Center for Immunization and Respiratory Diseases (proposed); A Wasley, PhD, Div of Viral Hepatitis; and N Jain, MD, Div of STD Prevention, National Center for HIV, Viral Hepatitis, STDs, and Tuberculosis Prevention (proposed), CDC. References
* 1) "What are your chances of getting HIV (the virus that causes AIDS)? Would you say high, medium, low, or none?"; 2) "In the past five years, have you had an STD other than HIV or AIDS?"; 3) "Tell me if any of these statements is true for you; do not tell me which statement or statements are true for you; just if any of them are: a) you have hemophilia and have received clotting factor concentrations; b) you are a man who has had sex with other men, even just one time; c) you have taken street drugs by needle, even just one time; d) you have traded sex for money or drugs, even just one time; e) you have tested positive for HIV (the virus that causes AIDS); f) you have had sex (even just one time) with someone who would answer `yes' to any of these statements."
Disclaimer All MMWR HTML versions of articles are electronic conversions from ASCII text into HTML. This conversion may have resulted in character translation or format errors in the HTML version. Users should not rely on this HTML document, but are referred to the electronic PDF version and/or the original MMWR paper copy for the official text, figures, and tables. An original paper copy of this issue can be obtained from the Superintendent of Documents, U.S. Government Printing Office (GPO), Washington, DC 20402-9371; telephone: (202) 512-1800. Contact GPO for current prices. **Questions or messages regarding errors in formatting should be addressed to mmwrq@cdc.gov.Date last reviewed: 5/11/2006 |
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