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Hepatitis B Virus: A Comprehensive Strategy for Eliminating Transmission in the United States Through Universal Childhood Vaccination: Recommendations of the Immunization Practices Advisory Committee (ACIP)

Immunization Practices Advisory Committee

Membership List, September 1991


Samuel L. Katz, M.D. John La Montagne, Ph.D. Duke University Medical Center National Institutes of Health


Food and Drug Administration Claire V. Broome, M.D. Centers for Disease Control LIAISON REPRESENTATIVES

MEMBERS American Academy of Family Physicians

Ronald C. Van Buren, M.D.

  • Stanley E. Broadnax, M.D. Columbus, Ohio Cincinnati Health Department

American Academy of Pediatrics

  • James D. Cherry, M.D. Georges Peter, M.D. University of California School Providence, Rhode Island

of Medicine (Los Angeles)

Caroline B. Hall, M.D. Mary Lou Clements, M.D. Rochester, New York Johns Hopkins University (Baltimore, Maryland) American College of Physicians

Pierce Gardner, M.D. David W. Fraser, M.D. Stonybrook, New York Swarthmore College (Pennsylvania) American Hospital Association

William Schaffner, M.D.

  • Caroline B. Hall, M.D. Nashville, Tennessee University of Rochester

School of Medicine and American Medical Association

Dentistry (New York) Edward A. Mortimer, Jr., M.D.

Cleveland, Ohio Carlos E. Hernandez, M.D. Kentucky Department for Canadian National Advisory Committee

Health Services on Immunization

Susan E. Tamblyn, M.D., Dr. P.H. Gregory R. Istre, M.D. Stratford, Ontario Medical City Hospital Canada (Dallas, Texas)

Department of Defense Carlos H. Ramirez-Ronda, M.D. Michael Peterson, D.V.M. University of Puerto Rico M.P.H., Dr. P.H.

School of Medicine (San Juan) Washington, D.C.

Mary E. Wilson, M.D. National Vaccine Program Mount Auburn Hospital Kenneth J. Bart, M.D. (Cambridge, Massachusetts) Rockville, Maryland

  • Terms expired 6/30/91.

The following statement updates all previous recommendations on protection against hepatitis B virus infection, including use of hepatitis B vaccine and hepatitis B immune globulin for prophylaxis against hepatitis B virus infection (MMWR 1985;34:313-24, 329-35, MMWR 1987;36:353-66, and MMWR 1990;39{No. RR-2}:8-19) and universal screening of pregnant women to prevent perinatal hepatitis B virus transmission (MMWR 1988;37:341-46, 51, and MMWR 1990;39{No. RR-2}:8-19). Recommendations concerning the prevention of other types of viral hepatitis are found in MMWR 1990;39(No. RR-2): 1-8, 22-26.

This document provides the rationale for a comprehensive strategy to eliminate transmission of hepatitis B virus in the United States. This prevention strategy includes making hepatitis B vaccine a part of routine vaccination schedules for all infants.


The acute and chronic consequences of hepatitis B virus (HBV) infection are major health problems in the United States. The reported incidence of acute hepatitis B increased by 37% from 1979 to 1989, and an estimated 200,000-300,000 new infections occurred annually during the period 1980- 1991. The estimated 1 million-1.25 million persons with chronic HBV infection in the United States are potentially infectious to others. In addition, many chronically infected persons are at risk of long-term sequelae, such as chronic liver disease and primary hepatocellular carcinoma; each year approximately 4,000-5,000 of these persons die from chronic liver disease (1).

Immunization with hepatitis B vaccine is the most effective means of preventing HBV infection and its consequences. In the United States, most infections occur among adults and adolescents (2,3). The recommended strategy for preventing these infections has been the selective vaccination of persons with identified risk factors (1,2). However, this strategy has not lowered the incidence of hepatitis B, primarily because vaccinating persons engaged in high-risk behaviors, life-styles, or occupations before they become infected generally has not been feasible. In addition, many infected persons have no identifiable source for their infections and thus cannot be targeted for vaccination (2).

Preventing HBV transmission during early childhood is important because of the high likelihood of chronic HBV infection and chronic liver disease that occurs when children less than 5 years of age become infected (3). Testing to identify pregnant women who are hepatitis B surface antigen (HBsAg)-positive and providing their infants with immunoprophylaxis effec- tively prevents HBV transmission during the perinatal period (4,5). Integrating hepatitis B vaccine into childhood vaccination schedules in populations with high rates of childhood infection (e.g., Alaskan Natives and Pacific Islanders) has been shown to interrupt HBV transmission (6).

This document provides the rationale for a comprehensive strategy to eliminate transmission of HBV and ultimately reduce the incidence of hepatitis B and hepatitis B-associated chronic liver disease in the United States. The recommendations for implementing this strategy include making hepatitis B vaccine a part of routine vaccination schedules for infants.


Infections among Infants and Children

In the United States, children become infected with HBV through a variety of means. The risk of perinatal HBV infection among infants born to HBV-infected mothers ranges from 10% to 85%, depending on each mother's hepatitis B e antigen (HBeAg) status (3,7,8). Infants who become infected by perinatal transmission have a 90% risk of chronic infection, and up to 25% will die of chronic liver disease as adults (9). Even when not infected during the perinatal period, children of HBV-infected mothers remain at high risk of acquiring chronic HBV infection by person-to-person (horizontal) transmission during the first 5 years of life (10). More than 90% of these infections can be prevented if HBsAg-positive mothers are identified so that their infants can receive hepatitis B vaccine and hepatitis B immune globulin (HBIG) soon after birth (4,5).

Because screening selected pregnant women for HBsAg has failed to identify a high proportion of HBV-infected mothers (11,12), prenatal HBsAg testing of all pregnant women is now recommended (1,13,14). Universal prenatal testing would identify an estimated 22,000 HBsAg-positive women and could prevent at least 6,000 chronic HBV infections annually (3). Screening and vaccination programs for women and infants receiving care in the public sector have already been initiated through state immunization projects.

Horizontal transmission of HBV during the first 5 years of life occurs frequently in populations in which HBV infection is endemic. The risk of chronic infection is age dependent, ranging from 30% to 60% for children 1-5 years of age (15). Worldwide, it has been recommended that, in popula- tions in which HBV infection is acquired during childhood, hepatitis B vaccine should be integrated into routine vaccination schedules for infants, usually as a part of the World Health Organization's Expanded Programme on Immunization (16). In the United States, racial/ethnic groups shown to have high rates of childhood HBV infection include Alaskan Natives (6,17), Pacific Islanders (18), and infants of first-generation immigrant mothers from parts of the world where HBV infection is endemic, especially Asia (19,20). Vaccination programs to prevent perinatal, childhood, and adult HBV infections among Alaskan Natives were begun in late 1982; as a result, the incidence of acute hepatitis B in this population has declined by over 99% (6). Hepatitis B vaccine was integrated into vaccination schedules for infants in American Samoa beginning in 1986 and by 1990 was incorporated into the schedules of the remaining Pacific Islands under U.S. jurisdiction.

Each year, approximately 150,000 infants are born to women who have immigrated to the United States from areas of the world where HBV infection is highly endemic (3). Children born to HBsAg-positive mothers can be identified through prenatal screening programs. However, children born to HBsAg-negative immigrant mothers are still at high risk of acquiring HBV infection, usually from other HBV carriers in their families or communities (3,19,20). Infections among these children can be prevented by making hepatitis B vaccine part of their routine infant vaccinations (1).

Infections among Adolescents and Adults

In the United States most persons with hepatitis B acquire the infection as adolescents or adults. Several specific modes of transmission have been identified, including sexual contact, especially among homosexual men and persons with multiple heterosexual partners; parenteral drug use; occupational exposures; household contact with a person who has an acute infection or with a chronic carrier; receipt of certain blood products; and hemodialysis. However, over one-third of patients with acute hepatitis B do not have readily identifiable risk factors (1,2).

The rates of HBV infection differ significantly among various racial and ethnic groups (2,21). For example, the prevalence of infection among adolescents and adults has been shown to be threefold to fourfold greater for blacks than for whites and to be associated with serologic evidence of previous infection with syphilis (21,22).

Efforts to vaccinate persons in the major risk groups have had limited success. For example, programs directed at injecting drug users failed to motivate them to receive three doses of vaccine (CDC, unpublished data). Health-care providers are often not aware of groups at high risk of HBV infection and frequently do not identify candidates for vaccination during routine health-care visits (CDC, unpublished data). In addition, there has been limited vaccination of susceptible household and sexual contacts of HBsAg carriers identified in screening programs for blood donors (23). Hepatitis B vaccination of health-care workers appears to have resulted in a substantial decrease in the rate of disease in this group, but has had little effect on overall rates of hepatitis B (2). Moreover, to achieve widespread vaccination of persons at occupational risk, regulations have had to be developed to ensure implementation of vaccination programs (24).

Educational programs to reduce parenteral drug use and unprotected sexual activity are important components of the strategy to prevent infection with the human immunodeficiency virus (HIV), which causes acquired immunodeficiency syndrome. These programs appear to have reduced the risk of HBV infections among homosexual men but have not had an impact on hepatitis B attributable to parenteral drug use or heterosexual trans- mission (2). Educational efforts alone are not likely to fully eliminate the high-risk behaviors responsible for HBV transmission.


Hepatitis delta virus (HDV) is a defective virus that causes infection only in the presence of active HBV infection (25). HDV infection occurs as either coinfection with HBV or superinfection of an HBV carrier. Coinfec- tion usually resolves; superinfection, however, frequently causes chronic HDV infection and chronic active hepatitis. Both types of infection may cause fulminant hepatitis.

Routes of transmission are similar to those of HBV. In the United States, HDV infection most commonly affects persons at high risk of HBV infection, particularly injecting drug users and persons receiving clotting factor concentrates (26). Preventing acute and chronic HBV infection of susceptible persons will also prevent HDV infection.


A comprehensive strategy to prevent HBV infection, acute hepatitis B, and the sequelae of HBV infection in the United States must eliminate transmission that occurs during infancy and childhood, as well as during adolescence and adulthood. In the United States it has become evident that HBV transmission cannot be prevented through vaccinating only the groups at high risk of infection. No current medical treatment will reliably eliminate chronic HBV infection and thus eliminate the source of new infections in susceptible persons (27). Therefore, new infections can be prevented only by immunizing susceptible persons with hepatitis B vaccine. Routine visits for prenatal and well-child care can be used to target hepatitis B prevention. A comprehensive prevention strategy includes a) prenatal testing of pregnant women for HBsAg to identify newborns who require immunoprophylaxis for the prevention of perinatal infection and to identify household contacts who should be vaccinated, b) routine vaccin- ation of children born to HBsAg-negative mothers, c) vaccination of certain adolescents, and d) vaccination of adults at high risk of infection.

Infants and children can receive hepatitis B vaccine during routine health-care visits; no additional visits would be required. Costs include that of the vaccine and the incremental expense associated with delivering an additional vaccine during a scheduled health-care visit. Implementation of this immunization strategy would be greatly facilitated by the develop- ment and use of multiple-antigen vaccines (e.g., diphtheria-tetanus- pertussis {DTP}/hepatitis B, Haemophilus influenzae type b conjugate/ hepatitis B). These vaccines would reduce the number of injections received by the infant, reduce the cost of administration, and greatly facilitate widespread vaccine delivery.

Since most HBV infections occur among adults, disease control could be accelerated by vaccinating emerging at-risk populations, such as adoles- cents and susceptible contacts of chronic HBV carriers. The recommendation for universal infant vaccination neither precludes vaccinating adults identified to be at high risk of infection nor alters previous recommen- dations for postexposure prophylaxis for hepatitis B (1).

The reduction in acute hepatitis B and hepatitis B-associated chronic liver disease resulting from universal infant vaccination may not become apparent for a number of years. However, universal HBsAg screening of pregnant women to prevent perinatal HBV infection has been shown to be cost saving (28, CDC, unpublished data), and the estimated cost of universal hepatitis B vaccination for infants is less than the direct medical and work-loss costs associated with the estimated 5% lifetime risk of infection (CDC, unpublished data). Currently, the cost of an infant's dose of hepatitis B vaccine delivered in the public sector is about the same as each of the other childhood vaccinations. Vaccinating adolescents and adults is substantially more expensive because of the higher vaccine cost and the higher implementation costs of delivering vaccine to target populations. In the long term, universal infant vaccination would eliminate the need for vaccinating adolescents and high-risk adults.


Two types of products are available for prophylaxis against HBV infection. Hepatitis B vaccine, which provides long-term protection against HBV infection, is recommended for both preexposure and postexposure prophylaxis. HBIG provides temporary protection (i.e., 3-6 months) and is indicated only in certain postexposure settings.

Hepatitis B Immune Globulin

HBIG is prepared from plasma known to contain a high titer of antibody against HBsAg (anti-HBs). In the United States, HBIG has an anti-HBs titer of >100,000 by radioimmunoassay. The human plasma from which HBIG is prepared is screened for antibodies to HIV; in addition, the process used to prepare HBIG inactivates and eliminates HIV from the final product. There is no evidence that HIV can be transmitted by HBIG (29,30).

Hepatitis B Vaccine

Two types of hepatitis B vaccine have been licensed in the United States. One, which was manufactured from the plasma of chronically infected persons, is no longer produced in the United States. The currently available vaccines are produced by recombinant DNA technology.

The recombinant vaccines are produced by using HBsAg synthesized by Saccharomyces cerevisiae (common bakers' yeast), into which a plasmid containing the gene for HBsAg has been inserted. Purified HBsAg is obtained by lysing the yeast cells and separating HBsAg from the yeast components by biochemical and biophysical techniques. Hepatitis B vaccines are packaged to contain 10-40 ug of HBsAg protein/mL after adsorption to aluminum hydroxide (0.5 mg/mL); thimerosal (1:20,000 concentration) is added as a preservative.

Routes and sites of administration.

The recommended series of three intramuscular doses of hepatitis B vaccine induces a protective antibody response (anti-HBs >=10 milli-inter- national units {mIU}/mL) in >90% of healthy adults and in >95% of infants, children, and adolescents (31-33). Hepatitis B vaccine should be admin- istered only in the deltoid muscle of adults and children or in the antero- lateral thigh muscle of neonates and infants; the immunogenicity of the vaccine for adults is substantially lower when injections are administered in the buttock (34). When hepatitis B vaccine is administered to infants at the same time as other vaccines, separate sites in the anterolateral thigh may be used for the multiple injections. This method is preferable to administering vaccine at sites such as the buttock or deltoid.

Compared with three standard doses admistered intramuscularly, three low doses of plasma-derived or recombinant vaccine administered intra- dermally to adults result in lower seroconversion rates (55%-81%) and lower final titers of anti-HBs (35-38), although four doses of plasma-derived vaccine administered intradermally have produced responses comparable with vaccine administered intramuscularly (39). Plasma-derived vaccine admin- istered intradermally to infants and children does not induce an adequate antibody response (40). At this time, low-dose intradermal vaccination of adults should be performed only under research protocol with written informed consent. Persons who have been vaccinated intradermally should be tested for anti-HBs. Those with an inadequate response (anti-HBs <10 mIU/ mL) should be revaccinated with three full doses of vaccine administered intramuscularly. Intradermal vaccination should not be used for infants or children.

Vaccination during pregnancy.

On the basis of limited experience, there is no apparent risk of adverse effects to developing fetuses when hepatitis B vaccine is admin- istered to pregnant women (CDC, unpublished data). The vaccine contains noninfectious HBsAg particles and should cause no risk to the fetus. HBV infection affecting a pregnant woman may result in severe disease for the mother and chronic infection for the newborn. Therefore, neither pregnancy nor lactation should be considered a contraindication to vaccination of women.

Vaccine Usage

Preexposure prophylaxis

Vaccination schedule and dose. The vaccination schedule most often used for adults and children has been three intramuscular injections, the second and third administered 1 and 6 months, respectively, after the first. An alternate schedule of four doses has been approved for one vaccine that would allow more rapid induction of immunity. However, for preexposure prophylaxis, there is no clear evidence that this regimen provides greater protection than that obtained with the standard three-dose schedule.

Each vaccine has been evaluated to determine the age-specific dose at which an optimum antibody response is achieved. The recommended dose varies by product and the recipient's age and, for infants, by the mother's HBsAg serologic status (Table_1). In general, the vaccine dose for children and adolescents is 50%-75% lower than that required for adults (Table_1).

Incorporating hepatitis B vaccine into childhood vaccination schedules may require modifications of previously recommended schedules. However, a protective level of anti-HBs (>=10 mIU/mL) was achieved when hepatitis B vaccine was administered in a variety of schedules, including those in which vaccination was begun soon after birth (5,8,41).

In a three-dose schedule, increasing the interval between the first and second doses of hepatitis B vaccine has little effect on immunogenicity or final antibody titer. The third dose confers optimal protection, acting as a booster dose. Longer intervals between the last two doses (4-12 months) result in higher final titers of anti-HBs (42,43). Several studies have shown that the currently licensed vaccines produce high rates of serocon- version (>95%) and induce adequate levels of anti-HBs when administered to infants at birth, 2 months, and 6 months of age or at 2 months, 4 months, and 6 months of age (CDC, Merck Sharpe & Dohme, SmithKline Beecham, unpub- lished data). When the vaccine is administered in four doses at 0, 1, 2, and 12 months, the last dose is necessary to ensure the highest final antibody titer.

When hepatitis B vaccine has been administered at the same time as other vaccines, no interference with the antibody response of the other vaccines has been demonstrated (44).

If the vaccination series is interrupted after the first dose, the second dose should be administered as soon as possible. The second and third doses should be separated by an interval of at least 2 months. If only the third dose is delayed, it should be administered when convenient.

The immune response when one or two doses of a vaccine produced by one manufacturer are followed by subsequent doses from a different manufacturer has been shown to be comparable with that resulting from a full course of vaccination with a single vaccine.

Larger vaccine doses or an increased number of doses are required to induce protective antibody in a high proportion of hemodialysis patients (45,46) and may also be necessary for other immunocompromised persons (e.g., those who take immunosuppressive drugs or who are HIV positive), although few data are available concerning response to higher doses of vaccine by these patients (47).

Prevaccination testing for susceptibility. Susceptibility testing is not indicated for immunization programs for children or for most adoles- cents because of the low rate of HBV infection and the relatively low cost of vaccine. For adults, the decision to do prevaccination testing should include an analysis of cost effectiveness because of the higher cost of the vaccine. Testing for prior infection should be considered for adults in risk groups with high rates of HBV infection (e.g., injecting drug users, homosexual men, and household contacts of HBV carriers). The decision for testing should be based on whether the costs of testing balance the costs of vaccine saved by not vaccinating already-infected persons. Estimates of the cost effectiveness of testing depend on three variables: the cost of vaccination, the cost of testing for susceptibility, and the expected prevalence of immune persons. If susceptibility testing is being considered, careful attention should also be given to the likelihood of patient follow-up and vaccine delivery.

For routine testing, only one antibody test is necessary (antibody either to the core antigen {anti-HBc} or anti-HBs). Anti-HBc testing identifies all previously infected persons, including HBV carriers, but does not differentiate carriers and non-carriers. The presence of anti-HBs identifies previously infected persons, except for HBV carriers. Neither test has a particular advantage for groups expected to have HBV carrier rates <2%, such as health-care workers. Anti-HBc may be preferable so that unnecessary vaccination of HBV carriers can be avoided in groups with high carrier rates.

Postvaccination testing for serologic response. Such testing is not necessary after routine vaccination of infants, children, or adolescents. Testing for immunity is advised only for persons whose subsequent clinical management depends on knowledge of their immune status (e.g., infants born to HBsAg-positive mothers, dialysis patients and staff, and persons with HIV infection). Postvaccination testing should also be considered for persons at occupational risk who may have exposures from injuries with sharp instruments, because knowledge of their antibody response will aid in determining appropriate postexposure prophylaxis. When necessary, postvac- cination testing should be performed from 1 to 6 months after completion of the vaccine series. Testing after immunoprophylaxis of infants born to HBsAg-positive mothers should be performed from 3 to 9 months after the completion of the vaccination series (see section on Postexposure prophylaxis).

Revaccination of nonresponders. When persons who do not respond to the primary vaccine series are revaccinated, 15%-25% produce an adequate antibody response after one additional dose and 30%-50% after three additional doses (48). Therefore, revaccination with one or more additional doses should be considered for persons who do not respond to vaccination initially.

Postexposure prophylaxis

After a person has been exposed to HBV, appropriate immunoprophylactic treatment can effectively prevent infection. The mainstay of postexposure immunoprophylaxis is hepatitis B vaccine, but in some settings the addition of HBIG will provide some increase in protection. Table_2 provides a guide to recommended treatment for various HBV exposures.

Transmission of perinatal HBV infection can be effectively prevented if the HBsAg-positive mother is identified and if her infant receives appro- priate immunoprophylaxis. Hepatitis B vaccination and one dose of HBIG, administered within 24 hours after birth, are 85%-95% effective in preventing both HBV infection and the chronic carrier state (4,5,8). Hepatitis B vaccine administered alone in either a three-dose or four-dose schedule (Table_1), beginning within 24 hours after birth, is 70%-95% effective in preventing perinatal HBV infections (8,41). The infants of women admitted for delivery who have not had prenatal HBsAg testing pose problems in clinical management. Initiating hepatitis B vaccination at birth for infants born to these women will provide adequate postexposure prophylaxis if the mothers are indeed HBsAg positive. The few infections not prevented by either of these treatment regimens were most likely acquired in utero or may be due to very high levels of maternal HBV-DNA (49).

Serologic testing of infants who receive immunoprophylaxis to prevent perinatal infection should be considered as an aid in the long-term medical management of the few infants who become HBV carriers. Testing for anti-HBs and HBsAg at 9-15 months of age will determine the success of the therapy and, in the case of failure, will identify HBV carriers or infants who may require revaccination.

Recommendations for postexposure prophylaxis in circumstances other than the perinatal period (Table_2) have been addressed in a previous statement and are reprinted as Appendix A to this document.

Vaccine Efficacy and Booster Doses

Clinical trials of the hepatitis B vaccines licensed in the United States have shown that they are 80%-95% effective in preventing HBV infection and clinical hepatitis among susceptible children and adults (5,33,41,50). If a protective antibody response develops after vaccination, vaccine recipients are virtually 100% protected against clinical illness.

The duration of vaccine-induced immunity has been evaluated in long- term follow-up studies of both adults and children (48,51). Only the plasma-derived hepatitis B vaccine has been evaluated because it has had the longest clinical use; however, on the basis of comparable immunogen- icity and short-term efficacy, similar results would be expected with recombinant vaccines. The magnitude of the antibody response induced by the primary vaccination series is predictive of antibody persistence, and a logarithmic decline of antibody levels occurs over time. Among young adults (homosexual men and Alaskan Eskimos) who initially responded to a three- dose vaccine series, loss of detectable antibody has ranged from 13% to 60% after 9 years of follow-up. For children vaccinated after the first year of life, the rate of antibody decline has been lower than for adults (51). The peak antibody titers for infants are lower than those for children immunized after 12 months of age, but the rate of antibody decline is comparable with that observed for adults in the same population.

Long-term studies of healthy adults and children indicate that immuno- logic memory remains intact for at least 9 years and confers protection against chronic HBV infection, even though anti-HBs levels may become low or decline below detectable levels (48,51,52). In these studies, the HBV infections were detected by the presence of anti-HBc. No episodes of clinical hepatitis were reported and HBsAg was not detected, although brief episodes of viremia may not have been detected because of infrequent testing. The mild, inapparent infections among persons who have been previously vaccinated should not produce the sequelae associated with chronic HBV infection and should provide lasting immunity. In general, follow-up studies of children vaccinated at birth to prevent perinatal HBV infection have shown that a continued high level of protection from chronic HBV infections persists at least 5 years (52,53).

For children and adults whose immune status is normal, booster doses of vaccine are not recommended, nor is serologic testing to assess antibody levels necessary. The possible need for booster doses will be assessed as additional information becomes available. For hemodialysis patients, vaccine-induced protection may be less complete and may persist only as long as antibody levels are >=10 mIU/mL. For these patients, the need for booster doses should be assessed by annual antibody testing, and a booster dose should be administered when antibody levels decline to <10 mIU/mL.

Vaccine Side Effects and Adverse Reactions

Hepatitis B vaccines have been shown to be safe when administered to both adults and children. Over 4 million adults have been vaccinated in the United States, and at least that many children have received hepatitis B vaccine worldwide.

Vaccine-associated side effects

Pain at the injection site (3%-29%) and a temperature greater than 37.7 C (1%-6%) have been among the most frequently reported side effects among adults and children receiving vaccine (5,31-33,50). In placebo-controlled studies, these side effects were reported no more frequently among vaccinees than among persons receiving a placebo (33,50). Among children receiving both hepatitis B vaccine and DTP vaccine, these mild side effects have been observed no more frequently than among children receiving DTP vaccine alone.

Serious adverse events

In the United States, surveillance of adverse reactions has shown a possible association between Guillain-Barre syndrome (GBS) and receipt of the first dose of plasma-derived hepatitis B vaccine (54, CDC unpublished data). GBS was reported at a very low rate (0.5/100,000 vaccinees), no deaths were reported, and all reported cases were among adults. An estimated 2.5 million adults received one or more doses of recombinant hepatitis B vaccine during the period 1986-1990. Available data from reporting systems for adverse events do not indicate an association between receipt of recombinant vaccine and GBS (CDC, unpublished data).

Until recently, large-scale hepatitis B vaccination programs for infants (e.g., Taiwan, Alaska, and New Zealand) have primarily used plasma- derived hepatitis B vaccine. No association has been found between vaccin- ation and the occurrence of severe adverse events, including seizures and GBS (55, B. McMahon and A. Milne, unpublished data). However, systematic surveillance for adverse reactions has been limited in these populations, and only a small number of children have received recombinant vaccine. Any presumed risk of adverse events possibly associated with hepatitis B vaccination must be balanced against the expected risk of acute and chronic liver disease associated with the current 5% lifetime risk of HBV infection in the United States. It is estimated that, for each U.S. birth cohort, 2,000-5,000 persons will die from HBV-related liver disease.

As hepatitis B vaccine is introduced for routine vaccination of infants, surveillance for vaccine-associated adverse events will continue to be an important part of the program in spite of the current record of safety. Any adverse event suspected to be associated with hepatitis B vaccination should be reported to the Vaccine Adverse Event Reporting System (VAERS). VAERS forms can be obtained by calling 1-800-822-7967.


Prevention of Perinatal Hepatitis B Virus Infection

  1. All pregnant women should be routinely tested for HBsAg during an early prenatal visit in each pregnancy, preferably at the same time other routine prenatal laboratory testing is done. HBsAg testing should be repeated late in the pregnancy for women who are HBsAg negative but who are at high risk of HBV infection (e.g., injecting drug users, those with intercurrent sexually transmitted diseases) or who have had clinically apparent hepatitis. Tests for other HBV markers are not necessary for the purpose of maternal screening. However, HBsAg- positive women identified during screening may have HBV-related liver disease and should be evaluated (56).

  2. Infants born to mothers who are HBsAg positive should receive the appropriate doses of hepatitis B vaccine (Table_1) and HBIG (0.5 mL) within 12 hours of birth. Both should be administered by intra- muscular injection. Hepatitis B vaccine should be administered concur- rently with HBIG but at a different site. Subsequent doses of vaccine should be administered according to the recommended schedule (Table_3).

  3. Women admitted for delivery who have not had prenatal HBsAg testing should have blood drawn for testing. While test results are pending, the infant should receive hepatitis B vaccine within 12 hours of birth, in a dose appropriate for infants born to HBsAg-positive mothers (Table_1).

    1. If the mother is later found to be HBsAg positive, her infant should receive the additional protection of HBIG as soon as possible and within 7 days of birth, although the efficacy of HBIG administered after 48 hours of age is not known (57). If HBIG has not been administered, it is important that the infant receive the second dose of hepatitis B vaccine at 1 month and not later than 2 months of age because of the high risk of infection. The last dose should be administered at age 6 months (Table_3). *

    2. If the mother is found to be HBsAg negative, her infant should continue to receive hepatitis B vaccine as part of his or her routine vaccinations (Table_3 and Table_4), in the dose appropriate for infants born to HBsAg-negative mothers (Table_1).

  4. In populations in which screening pregnant women for HBsAg is not feasible, all infants should receive their first dose of hepatitis B vaccine within 12 hours of birth, their second dose at 1-2 months of age, and their third dose at 6 months of age as a part of their childhood vaccinations and well-child care (Table_3).

  5. Household contacts and sex partners of HBsAg-positive women identified through prenatal screening should be vaccinated. The decision to do prevaccination testing of these contacts to determine susceptibility to HBV infection should be made according to the guidelines in the section "Prevaccination testing for susceptibility." Hepatitis B vaccine should be administered at the age-appropriate dose (Table_1) to those determined to be susceptible or judged likely to be susceptible to infection.

Universal Vaccination of Infants Born to HBsAg-Negative Mothers

  1. Hepatitis B vaccination is recommended for all infants, regardless of the HBsAg status of the mother. Hepatitis B vaccine should be incor- porated into vaccination schedules for children. The first dose can be administered during the newborn period, preferably before the infant is discharged from the hospital, but no later than when the infant is 2 months of age (Table_4). Because the highest titers of anti-HBs are achieved when the last two doses of vaccine are spaced at least 4 months apart, schedules that achieve this spacing may be preferable (Table_4). However, schedules with 2-month intervals between doses, which conform to schedules for other childhood vaccines, have been shown to produce a good antibody response (Table_4) and may be appropriate in populations in which it is difficult to ensure that infants will be brought back for all their vaccinations. The develop- ment of combination vaccines containing HBsAg may lead to other schedules that will allow optimal use of combined antigens.

  2. Special efforts should be made to ensure that high levels of hepatitis B vaccination are achieved in populations in which HBV infection occurs at high rates among children (Alaskan Natives, Pacific Islanders, and infants of immigrants from countries in which HBV is endemic).

Vaccination of Adolescents

All adolescents at high risk of infection because they are injecting drug users or have multiple sex partners (more than one partner/6 months) should receive hepatitis B vaccine. Widespread use of hepatitis B vaccine is encouraged. Because risk factors are often not identified directly among adolescents, universal hepatitis B vaccination of teenagers should be implemented in communities where injecting drug use, pregnancy among teenagers, and/or sexually transmitted diseases are common. Adolescents can be vaccinated in school-based clinics, community health centers, family planning clinics, clinics for the treatment of sexually transmitted diseases, and special adolescent clinics.

The 0-, 1-, and 6-month schedule is preferred for vaccinating adoles- cents with the age-appropriate dose of vaccine (Table_1). However, the choice of vaccination schedule should take into account the feasibility of delivering three doses of vaccine over a given period of time. The use of alternate schedules (e.g., 0, 2, and 4 months) may be advisable to achieve complete vaccination.

Vaccination of Selected High-Risk Groups

Efforts to vaccinate persons at high risk of HBV infection should follow the vaccine doses shown in Table_1. High-risk groups for whom vaccination is recommended include:

  1. Persons with occupational risk. HBV infection is an occupational hazard for health-care workers and for public-safety workers who have exposure to blood in the workplace (24,58). The risk of acquiring HBV infections from occupational exposures depends on the frequency of percutaneous and permucosal exposure to blood or blood-contaminated body fluids. Any health-care or public-safety worker may be at risk for HBV exposure, depending on the tasks he or she performs. Workers who perform tasks involving contact with blood or blood-contaminated body fluid should be vaccinated (24,58, 59). For public-safety workers whose exposure to blood is infrequent, timely postexposure prophylaxis should be considered rather than routine preexposure vaccination.

    For persons in health-care fields, vaccination should be completed during training in schools of medicine, dentistry, nursing, laboratory technology, and other allied health professions, before trainees have their first contact with blood.

  2. Clients and staff of institutions for the developmentally disabled. Susceptible clients in institutions for the developmentally disabled, as well as staff who work closely with clients, should be vaccinated. Susceptible clients and staff who live or work in smaller residential settings with known HBV carriers should also receive hepatitis B vaccine. Clients discharged from residential institutions into community programs should be screened for HBsAg so that appropriate measures can be taken to prevent HBV trans- mission. These measures should include both environmental controls and appropriate use of vaccine.

    Staff of nonresidential day-care programs for the develop- mentally disabled (e.g., schools, sheltered workshops) attended by known HBV carriers have a risk of infection comparable with that of health-care workers and therefore should be vaccinated (60). The risk of infection for other clients appears to be lower than the risk for staff. Vaccination of clients in day care programs may be considered. Vaccination of classroom contacts is strongly encouraged if a classmate who is an HBV carrier behaves aggres- sively or has special medical problems (e.g., exudative dermatitis, open skin lesions) that increase the risk of exposure to his or her blood or serous secretions.

  3. Hemodialysis patients. Hepatitis B vaccination is recommended for susceptible hemodialysis patients. Vaccinating patients early in the course of their renal disease is encouraged because patients with uremia who are vaccinated before they require dialysis are more likely to respond to the vaccine (61). Although their serocon- version rates and anti-HBs titers are lower than those of healthy persons, patients who respond to vaccination will be protected from infection, and the need for frequent serologic testing will be reduced (62).

  4. Recipients of certain blood products. Patients who receive clotting-factor concentrates have an increased risk of HBV infection and should be vaccinated as soon as their specific clotting disorder is identified. Prevaccination testing is recom- mended for patients who have already received multiple infusions of these products.

  5. Household contacts and sex partners of HBV carriers. All household and sexual contacts of persons identified as HBsAg positive should be vaccinated. The decision to do prevaccination testing to determine susceptibility to HBV infection should be made according to the guidelines described earlier in the section "Prevaccination testing for susceptibility." Hepatitis B vaccine should be admin- istered at the age-appropriate dose (Table_1) to those deter- mined to be susceptible or judged likely to be susceptible to infection.

  6. Adoptees from countries where HBV infection is endemic. Adopted or fostered orphans or unaccompanied minors from countries where HBV infection is endemic should be screened for HBsAg (3). If the children are HBsAg positive, other family members should be vaccinated (63).

  7. International travelers. Vaccination should be considered for persons who plan to spend more than 6 months in areas with high rates of HBV infection and who will have close contact with the local population. Short-term travelers who are likely to have contact with blood (e.g., in a medical setting) or sexual contact with residents of areas with high or intermediate levels of endemic disease should be vaccinated. Vaccination should begin at least 6 months before travel to allow for completion of the full vaccine series, although a partial series will offer some protection. The alternate four-dose schedule (see Table_1) should provide protection if the first three doses can be delivered before departure.

  8. Injecting drug users. All injecting drug users who are susceptible to HBV should be vaccinated as soon as their drug use begins. Because of the high rate of HBV infection in this population, prevaccination screening should be considered as outlined in the section "Prevaccination testing for susceptibility." Injecting drug users known to have HIV infection should be tested for anti-HBs response after completion of the vaccine series. Those who do not respond to vaccination should be counseled accordingly.

  9. Sexually active homosexual and bisexual men. Susceptible sexually active homosexual and bisexual men should be vaccinated. Because of the high rate of HBV infection in this population, prevaccination screening should be considered as described in the section "Prevac- cination testing for susceptibility." Men known to have HIV infection should be tested for anti-HBs response after completion of the vaccine series. Those who do not respond to vaccination should be counseled accordingly.

  10. Sexually active heterosexual men and women. Vaccination is recom- mended for men and women who are diagnosed as having recently acquired other sexually transmitted diseases, for prostitutes, and for persons who have a history of sexual activity with more than one partner in the previous 6 months (2). Most patients seen in clinics for sexually transmitted diseases should be considered candidates for vaccination.

  11. Inmates of long-term correctional facilities. Prison officials should consider undertaking screening and vaccination programs directed at inmates with histories of high-risk behaviors.


Hepatitis B vaccine has now been used extensively throughout the world and is currently being incorporated into the Expanded Programme on Immuni- zation of the World Health Organization (16). New information, vaccines, and technology will have implications for this effort, and adjustments and changes are expected to occur over the years. Some of the issues that can be expected to be addressed in clinical and operational studies include the following:

  1. In most developing countries with hepatitis B immunization programs, the first dose of vaccine is administered to all infants soon after birth to prevent perinatal infections; pregnant women are not screened for HBsAg; and HBIG is not used (8,16,45). The feasibility and effectiveness of incorporating this approach into the hepatitis B prevention strategy for the United States must be evaluated.

  2. Booster doses of hepatitis B vaccine have not been recommended because of the persistence of protective efficacy 9 years after vaccination (48,51). The duration of protective efficacy for adolescents who were vaccinated during infancy or childhood must be evaluated; the results will determine future recommendations concerning booster doses.

  3. Flexible dosage schedules are required to effectively integrate hepatitis B vaccine into current and future immunization programs for infants. Schedules may change as optimum dosage and timing are studied and new information becomes available.

  4. Multiple-antigen vaccines that incorporate HBsAg as one component are currently being evaluated. The routine use of these vaccines may alter childhood vaccination schedules or may result in the administration of additional doses of certain antigens. However, these vaccines should greatly facilitate vaccine delivery and minimize the number of injections.


  1. CDC. Protection against viral hepatitis: recommendations of the Immunization Practices Advisory Committee (ACIP). MMWR 1990;39:5-22.

  2. Alter MJ, Hadler SC, Margolis HS, et al. The changing epidemiology of hepatitis B in the United States: need for alternative vaccination strategies. JAMA 1990;263:1218-22.

  3. Margolis HS, Alter MJ, Hadler SC. Hepatitis B: evolving epidemiology and implications for control. Semin Liver Dis 1991;11:84-92.

  4. Stevens CE, Toy PT, Tong MJ, et al. Perinatal hepatitis B virus trans- mission in the United States: prevention by passive-active immuni- zation. JAMA 1985;253:1740-5.

  5. Stevens CE, Taylor PE, Tong MJ, et al. Yeast-recombinant hepatitis B vaccine: efficacy with hepatitis B immune globulin in prevention of perinatal hepatitis B virus transmission. JAMA 1987;257:2612-6.

  6. McMahon BJ, Rhoades ER, Heyward WL, et al. A comprehensive programme to reduce the incidence of hepatitis B virus infection and its sequelae in Alaskan Natives. Lancet 1987;2:1134-6.

  7. Stevens CE, Neurath RA, Beasley RP, Szmuness W. HBeAg and anti-HBe detection by radioimmunoassay: correlation with vertical transmission of hepatitis B virus in Taiwan. J Med Virol 1979;3:237-41.

  8. Xu Z-Y, Liu C-B, Francis DP, et al. Prevention of perinatal acquisition of hepatitis B virus carriage using vaccine: preliminary report of a randomized, double-blind placebo-controlled and comparative trial. Pediatrics 1985;76:713-8.

  9. Beasley RP, Hwang L-Y. Epidemiology of hepatocellular carcinoma. In: Vyas GN, Dienstag JL, Hoofnagle JH, eds. Viral hepatitis and liver disease. New York: Grune & Stratton, 1984:209-24.

  10. Beasley RP, Hwang L-Y. Postnatal infectivity of hepatitis B surface antigen-carrier mothers. J Infect Dis 1983;147:185-90.

  11. Jonas MM, Schiff ER, O'Sullivan MJ, et al. Failure of the Centers for Disease Control criteria to identify hepatitis B infection in a large municipal obstetrical population. Ann Intern Med 1987;107:335-7.

  12. Kumar ML, Dawson NV, McCullough AJ, et al. Should all pregnant women be screened for hepatitis B? Ann Intern Med 1987;107:273-7.

  13. American Academy of Pediatrics. Hepatitis B. In: Peter G, Lepow ML, McCracken GH, Phillips CF, eds. Report of the Committee on Infectious Diseases. 22nd ed. Elk Grove Village, IL: American Academy of Pedia- trics, 1991:238-55.

  14. American Academy of Pediatrics and American College of Obsterics and Gynecology. Guidelines for prenatal care. 3rd ed. Elk Grove Village, IL: American Academy of Pediatrics, 1991 (in press).

  15. McMahon BJ, Alward WLM, Hall DB, et al. Acute hepatitis B virus infection: relation of age to the clinical expression of disease and subsequent development of the carrier state. J Infect Dis 1985;151: 599-603.

  16. World Health Organization. Progress in the control of viral hepatitis: memorandum from a WHO meeting. Bull WHO 1988;66:443-55.

  17. Schreeder MT, Bender TR, McMahon BJ, et al. Prevalence of hepatitis B in selected Alaskan Eskimo villages. Am J Epidemiol 1983;118:543-9.

  18. Wong DC, Purcell RH, Rosen L. Prevalence of antibody to hepatitis A and hepatitis B viruses in selected populations of the South Pacific. Am J Epidemiol 1979;110:227-36.

  19. Franks AL, Berg CJ, Kane MA, et al. Hepatitis B virus infection among children born in the United States to Southeast Asian refugees. N Engl J Med 1989;321:1301-5.

  20. Hurie MB, Mast EE, Davis JP. Horizontal transmission of hepatitis B virus infection to United States-born children of Hmong refugees. Pediatrics 1992 (in press).

  21. McQuillan GM, Townsend TR, Fields HA, et al. The seroepidemiology of hepatitis B virus in the United States, 1976 to 1980. Am J Med 1989;87 (Suppl 3A):5-10.

  22. CDC. Racial differences in rates of hepatitis B virus infection -- United States, 1976-1980. MMWR 1989;38:818-21.

  23. Moyer LA, Shapiro CN, Shulman G, Brugliera P. A survey of hepatitis B surface antigen positive blood donors: degree of understanding and action taken after notification. In: Hollinger FB, Lemon SM, Margolis HS, eds. Viral hepatitis and liver disease. Baltimore: Williams & Wilkins, 1991:728-9.

  24. US Department of Labor, US Department of Health and Human Services. Joint Advisory Notice. Protection against exposure to hepatitis B virus (HBV) and human immunodeficiency virus (HIV). Federal Register 1987;52: 41818-24.

  25. Rizzetto M. The delta agent. Hepatology 1983;3:729-37.

  26. Hadler SC, Fields HA. Hepatitis delta virus. In: Belshe RB, ed. Textbook of human virology. St. Louis: Mosby Year Book, 1991:749-66.

  27. Perrillo RP, Schiff ER, Davis FL, et al. A randomized, controlled trial of interferon alfa-2b alone and after prednisone withdrawal for the treatment of chronic hepatitis B. N Engl J Med 1990;323:295-301.

  28. Arevalo JA, Washington E. Cost-effectiveness of prenatal screening and immunization for hepatitis B virus. JAMA 1988;259:365-9.

  29. CDC. Safety of therapeutic immune globulin preparations with respect to transmission for human T-lymphotrophic virus type III/lymphadenopathy- associated virus infection. MMWR 1986;35:231-3.

  30. Wells MA, Wittek AE, Epstein JS, et al. Inactivation and partition of human T-cell lymphotrophic virus, type III, during ethanol fraction- ation of plasma. Transfusion 1986;26:210-3.

  31. Zajac BA, West DJ, McAleer WJ, Scolnick EM. Overview of clinical studies with hepatitis B vaccine made by recombinant DNA. J Infect 1986;13(Suppl A):39-45.

  32. Andre FE. Summary of safety and efficacy data on a yeast-derived hepatitis B vaccine. Am J Med 1989;87(Suppl 3A):14s-20s.

  33. Szmuness W, Stevens CE, Harley EJ, et al. Hepatitis B vaccine: demon- stration of efficacy in a controlled clinical trial in a high-risk population in the United States. N Engl J Med 1980;303:833-41.

  34. Shaw FE Jr, Guess HA, Roets JM, et al. Effect of anatomic injection site, age, and smoking on the immune response to hepatitis B vaccination. Vaccine 1989;7:425-30.

  35. Redfield RR, Innis BL, Scott RM, Cannon HG, Bancroft WH. Clinical evaluation of low-dose intradermally administered hepatitis B vaccine, a cost reduction strategy. JAMA 1985;254:3203-6.

  36. Coleman PJ, Shaw FE Jr, Serovich J, Hadler SC, Margolis HS. Intradermal hepatitis B vaccination in a large hospital employee population. Vaccine 1991;9:723-7.

  37. Gonzalez ML, Usandizaga M, Alomar P, et al. Intradermal and intramus- cular route for vaccination against hepatitis B. Vaccine 1990;8:402-5.

  38. Lancaster D, Elam S, Kaiser AB. Immunogenicity of the intradermal route of hepatitis B vaccination with use of recombinant hepatitis B vaccine. Am J Infect Control 1989;17:126-9.

  39. King JW, Taylor EM, Crow SD, et al. Comparison of the immunogenicity of hepatitis B vaccine administered intradermally and intramuscularly. Rev Infect Dis 1990;12:1035-43.

  40. Xu Z-Y, Margolis HS. Determinants of hepatitis B vaccine efficacy and implications for vaccination strategies. Monogr Virol 1991 (in press).

  41. Poovorawan Y, Sanpavat S, Pongpuniert W, Chumdermpadetsuk S, Sentrakul P, Safary A. Protective efficacy of a recombinant DNA hepatitis B vaccine in neonates of HBe antigen-positive mothers. JAMA 1989;261: 3278-81.

  42. Jilg W, Schmidt M, Dienhardt F. Vaccination against hepatitis B: comparison of three different vaccination schedules. J Infect Dis 1989;160:766-9.

  43. Hadler SC, Monzon MA, Lugo DR, Perez M. Effect of timing of hepatitis B vaccine dose on response to vaccine in Yucpa Indians. Vaccine 1989;7: 106-10.

  44. Coursaget P, Yvonnet B, Relyveld EH, Barres JL, Diop-Mar I, Chiron JP. Simultaneous administration of diphtheria-tetanus-pertussis-polio and hepatitis B vaccines in a simplified immunization program: Immune response to diphtheria toxoid, tetanus toxoid, pertussis and hepatitis B surface antigen. Infect Immun 1986;151:784-7.

  45. Stevens CE, Alter HJ, Taylor PE, et al. Hepatitis B vaccine in patients receiving hemodialysis: immunogenicity and efficacy. N Engl J Med 1984; 311:496-501.

  46. Jilg W, Schmidt M, Weinel B, et al. Immunogenicity of recombinant hepatitis B vaccine in dialysis patients. J Hepatol 1986;3:190-5.

  47. Collier AC, Corey L, Murphy VL, Handsfield HH. Antibody to human immunodeficiency virus (HIV) and suboptimal response to hepatitis B vaccination. Ann Intern Med 1988;109:101-5.

  48. Hadler SC, Francis DP, Maynard JE, et al. Long-term immunogenicity and efficacy of hepatitis B vaccine in homosexual men. N Engl J Med 1986; 315:209-14.

  49. Lee S-D, Lo K-J, Wu J-C, et al. Prevention of maternal-infant hepatitis B virus transmission by immunization: role of serum hepatitis B virus DNA. Hepatology 1986;6:369-73.

  50. Francis DP, Hadler SC, Thompson SE, et al. Prevention of hepatitis B with vaccine: report from the Centers for Disease Control multi-center efficacy trial among homosexual men. Ann Intern Med 1982;97:362-6.

  51. Wainwright RB, McMahon BJ, Bulkow LR, et al. Duration of immunogenicity and efficacy of hepatitis B vaccine in a Yupik Eskimo population. JAMA 1989;261:2362-6.

  52. Lo K-J, Lee S-D, Tsai Y-T, et al. Long-term immunogenicity and efficacy of hepatitis B vaccine in infants born to HBeAg-positive HBsAg-carrier mothers. Hepatology 1988;8:1647-50.

  53. Hwang L-Y, Lee C-Y, Beasley RP. Five year follow-up of HBV vaccination with plasma-derived vaccine in neonates. Evaluation of immunogenicity and efficacy against perinatal transmission. In: Hollinger FB, Lemon SM, Margolis HS, eds. Viral hepatitis and liver disease. Baltimore: Williams & Wilkins, 1991:759-61.

  54. Shaw FE Jr, Graham DJ, Guess HA, et al. Postmarketing surveillance for neurologic adverse events reported after hepatitis B vaccination: experience of the first three years. Am J Epidemiol 1988;127:337-52.

  55. Chen D-S. Control of hepatitis B in Asia: mass immunization program in Taiwan. In: Hollinger FB, Lemon SM, Margolis HS, eds. Viral hepatitis and liver disease. Baltimore: Williams & Wilkins, 1991:716-9.

  56. CDC. Public Health Service inter-agency guidelines for screening donors of blood, plasma, organs, tissues and semen for evidence of hepatitis B and hepatitis C. MMWR 1991;40:5-6.

  57. Beasley RP, Hwang L-Y, Stevens CE, et al. Efficacy of hepatitis B immune globulin for prevention of perinatal transmission of the hepatitis B virus carrier state: final report of a randomized double- blind, placebo-controlled trial. Hepatology 1983;3:135-41.

  58. CDC. Guidelines for prevention of transmission of human immunodefi- ciency virus and hepatitis B virus to health-care and public-safety workers. MMWR 1989;38(Suppl 6):5-15.

  59. Department of Labor. Occupational exposure to bloodborne pathogens: proposed rule and notice of hearing. Federal Register 1989;54: 23042-139.

  60. Breuer B, Friedman SM, Millner ES, Kane MA, Snyder RH, Maynard JE. Transmission of hepatitis B virus in classroom contacts of mentally retarded carriers. JAMA 1985;254:3190-5.

  61. Seaworth B, Drucker J, Starling J, Drucker R, Stevens C, Hamilton J. Hepatitis B vaccines in patients with chronic renal failure before dialysis. J Infect Dis 1988;157:332-7.

  62. Moyer LA, Alter MJ, Favero MS. Hemodialysis-associated hepatitis B: revised recommendations for serologic screening. Semin Dialysis 1990;3: 201-4.

  63. Hershow RC, Hadler SC, Kane MA. Adoption of children from countries with endemic hepatitis B: transmission risks and medical issues. Pediatr Infect Dis J 1987;6:431-7.

If a four-dose schedule is used (Table_1 and Table_3), the second and third doses should be administered at 1 and 2 months of age, respec- tively, and the fourth dose at 12-18 months of age.

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TABLE 1. Recommended doses of currently licensed hepatitis B vaccines
                                  Recombivax HB *          Engerix-B *
                                 ------------------     ------------------
Group                            Dose (ug)   (mL)       Dose (ug)   (mL)
Infants of HBsAg + -negative
mothers and children
<11 years                            2.5    (0.25)         10      (0.5)

Infants of HBsAg-positive
mothers; prevention of               5      (0.5)          10      (0.5)
perinatal infection

Children and adolescents
11-19 years                          5      (0.5)          20      (1.0)

Adults >=20 years                   10      (1.0)          20      (1.0)

Dialysis patients and
other immunocompromised
persons                             40      (1.0) &        40      (2.0) @
* Both vaccines are routinely administered in a three-dose series. Engerix-B has also been
  licensed for a four-dose series administered at 0, 1, 2, and 12 months.
+ HBsAg = Hepatitis B surface antigen.
& Special formulation.
@ Two 1.0-mL doses administered at one site, in a four-dose schedule at 0, 1, 2, and 6 months.

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TABLE 2. Guide to postexposure immunoprophylaxis for exposure to hepatitis B virus
Type of exposure                       Immunoprophylaxis              Reference
Perinatal                              Vaccination + HBIG *           p. 11-12

Sexual -- acute infection              HBIG +/- Vaccination           Appendix

Sexual -- chronic carrier              Vaccination                    p. 12, 15

Household contact --
  chronic carrier                      Vaccination                    p. 12, 15

Household contact --                   None unless
  acute case                           known exposure                 Appendix

Household contact -- acute
  case, known exposure                 HBIG +/- vaccination           Appendix

Infant (<12 months) --
  acute case in primary                HBIG + vaccination
  care-giver                                                          Appendix

Inadvertent -- percutaneous/
  permucosal                           Vaccination +/- HBIG           Appendix
* HBIG = Hepatitis B immune globulin.

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TABLE 3. Recommended schedule of hepatitis B immunoprophylaxis to prevent
perinatal transmission of hepatitis B virus infection
Infant born to mother known to be HBsAg * positive
  Vaccine dose +                                   Age of infant
    First                                            Birth (within 12 hours)
    HBIG &                                           Birth (within 12 hours)
    Second                                           1 month
    Third                                            6 months @

Infant born to mother not screened for HBsAg
  Vaccine dose **                                  Age of infant
    First                                            Birth (within 12 hours)
    HBIG &                                           If mother is found to be HBsAg
                                                       positive, administer dose to
                                                       infant as soon as possible, not
                                                       later than 1 week after birth
    Second                                           1-2 months ++
    Third                                            6 months @
 * HBsAg = Hepatitis B surface antigen.
 + See Table 1 for appropriate vaccine dose.
 & Hepatitis B immune globulin (HBIG) -- 0.5 mL administered intramuscularly at a site different
   from that used for vaccine.
 @ If four-dose schedule (Engerix-B) is used, the third dose is administered at 2 months of age and
   the fourth dose at 12-18 months.
** First dose = dose for infant of HBsAg-positive mother (see Table 1). If mother is found to be
   HBsAg positive, continue that dose; if mother is found to be HBsAg negative, use appropriate
   dose from Table 1.
++ Infants of women who are HBsAg negative can be vaccinated at 2 months of age.

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TABLE 4. Recommended schedules of hepatitis B vaccination for infants born to
HBsAg * -negative mothers
      Hepatitis B vaccine                       Age of infant
      Option 1
        Dose 1                                  Birth -- before hospital discharge
        Dose 2                                  1-2 months +
        Dose 3                                  6-18 months +

      Option 2
        Dose 1                                  1-2 months +
        Dose 2                                  4 months +
        Dose 3                                  6-18 months +
* HBsAg = Hepatitis B surface antigen.
+ Hepatitis B vaccine can be administered simultaneously with diphtheria-tetanus-pertussis,
  Haemophilus influenzae type b conjugate, measles-mumps-rubella, and oral polio vaccines at
  the same visit.

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