Continuing Education Activity

The hepatitis B vaccine is a medication used in the prevention of hepatitis B infection, which can lead to chronic liver failure and hepatocellular carcinoma. It is in the vaccine class of drugs. This activity reviews the indications, action, and contraindications for the hepatitis B vaccine as a valuable agent in the prevention of hepatitis B infection. This activity will highlight the mechanism of action, adverse event profile, and other vital factors pertinent for members of the healthcare team in reducing the burden of hepatitis B on their patients and community.

Objectives:

• Review the mechanism of action and administration of the hepatitis B vaccine.
• Describe the adverse effects and contraindications of the hepatitis B vaccine.
• Explain the monitoring for patients receiving the hepatitis B vaccine and any toxicity.
• Outline the importance of improving care coordination amongst the healthcare team to enhance the delivery of care for patients receiving the hepatitis B vaccine.

Indications

Public health officials have ranked the reduction in vaccine-preventable diseases as one of the top 10 public health achievements in the 21 century.[1] Hepatitis B vaccine is an integral part of this achievement, and its role continues to evolve this century. Hepatitis B vaccination is indicated to prevent active infection with the hepatitis B virus, which can lead to chronic liver failure and hepatocellular carcinoma. The virus is highly infectious and can transmit through percutaneous or mucosal exposure to blood and body fluids. The virus even remains viable on environmental surfaces for more than seven days.[2]

The immunization program for hepatitis B changed significantly in 1991 in the United States with a big push to eradicate the infection and substantially reduce its resultant morbidity and mortality. In 1991, the United States started a strategy to achieve universal vaccination of infants beginning at birth for hepatitis B.[2] The vaccine has numerous other indications. In addition to all infants and any yet unvaccinated children, the Advisory Committee on Immunization Practices recommends primarily vaccinating any adults who may have a higher risk for contracting or complication from hepatitis B including[2]:

• Persons at risk for sexually transmitted disease
• Incarcerated persons
• Persons whose sex partner is hepatitis B surface antigen (HBsAg) positive
• HBsAg positive household contacts
• Men who have sex with men
• Intravenous drug users
• Healthcare workers, dialysis patients
• Persons with diabetes aged 19 to 59 years old
• Persons with hepatitis C
• Travelers to countries endemic for hepatitis B
• Persons with HIV
• Persons with chronic liver disease
• All persons seeking protection from hepatitis B

This strategy has been largely effective. The vaccination itself benefits not just the vaccinated but the entire community. The increasing immunization rate has shown to reduce morbidity and mortality from the virus.[1] From 2000 to 2014, the rate of acute hepatitis B infection in adults dropped by 50%.[1] This effect was mainly attributed to the herd immunity effect.[1]

Mechanism of Action

The vaccine is a noninfectious subunit of the virus, which leads to an active immunity.  Antibodies produced by vaccination target towards the outer protein coat or surface antigen. This leads to protection against all genotypes (A through H) of the virus and gives a broad immunity.[3]

Administration

Intramuscular injection is the preferred administration method. The intradermal route is not recommended. The preferred site of injection is the deltoid muscle. A regimen of three doses of the recombinant vaccine over six months is the current preferred method. A new vaccine has received approval for adults in the United States, which requires just two doses in one month.[1][3]

Adverse Effects

Research has demonstrated the hepatitis B vaccine to be safe for all age groups.[4] From 1982 to 2004, over 70 million persons received at least one dose of the vaccine in the United States, with the most reported side effects being: injection site pain (3 to 29%) and temperature greater than 99.9°F (1 to 6%).[5] These effects occurred at similar rates with persons receiving a placebo.[5] However, the Institute of Medicine in 2011 did conclude that evidence supports a causal relationship between the vaccine and anaphylaxis in persons with hypersensitivity to yeast.[5]

Contraindications

Hepatitis B vaccine is contraindicated in individuals with a history of hypersensitivity to any components of the vaccine or a yeast hypersensitivity.[5][4] Additionally, persons with a history of serious adverse events, such as anaphylaxis, after a previous hepatitis B vaccination (including combination vaccines) should not receive any further doses. Of note, the vaccine is not contraindicated in persons with a history of Guillain-Barre syndrome, autoimmune disease, current pregnancy, or lactation. The vaccine contains a noninfectious surface antigen, which poses no risk of transmission to the fetus.[4]

Monitoring

Hepatitis B surface antibody titers increase quickly following vaccination and then decrease over time.[1] More than 90% of immunized children develop protective antibody levels after the first dose.[5][6] An immunocompetent person receiving the complete series is generally protected indefinitely. The Advisory Committee on Immunization Practices (ACIP) does not generally recommend titers after vaccination, except for some health care workers and immunocompromised persons.[1] In health care workers at risk for occupational exposure, serologic testing is recommended 1 to 2 months after the last vaccine dose, and revaccination with ≥one dose is the recommendation for non-responders.[7][6] Health care workers who completed the vaccine series and had a subsequent positive titer (≥10 mIU/mL anti-HBs) are considered hepatitis B immune and do not need any further routine testing for protection so long as they remain immune-competent.[7] All persons receiving the vaccine should remain under observation for at least 15 minutes following its administration for syncope or signs of anaphylaxis.[3][5][4]

Toxicity

The vaccine is not known to have any dose-dependent toxicity. There is no antidote indicated for its management. 

Enhancing Healthcare Team Outcomes

The interprofessional health care team faces many challenges when vaccinating patients for hepatitis B. While few medical interventions have as great an impact on health as vaccinations, and the hepatitis B vaccination is generally safe, lack of knowledge about the vaccine by healthcare team members and patient concern about adverse events can decrease coverage. Challenges on knowledge of the vaccine for healthcare team members include staying current on evolving recommendations for whom the vaccine is indicated.[1][5][8] All team members can increase the vaccination rate of their patients by encouraging all staff to become trained in the assessment of vaccination histories and any pertinent staff in the administration of the vaccine. Protecting the time of staff to do this is an essential component of this strategy. All patients should receive education on the benefits of vaccination, including its herd immunity effect, the generally safe side effect profile, and the relatively few contraindications. A presumption of acceptance may be effective with most patients.[1][8] The hesitant parent and patient who does not respond to this can pose a challenge in vaccination.[8] Motivational interviewing techniques have shown to be effective with these hesitant patients.[1]

Nurses should always verify the patient's vaccination status regarding hepatitis B and report their findings to the clinician. Many states in the USA allow pharmacists to administer the vaccine, and pharmacists should reinforce the counsel from the provider and nursing staff, and update the patient's record with each dose. In this manner, the entire interprofessional team can operate from the same data regarding vaccination status, leading to better patient outcomes. [Level 5]

Of note, there is a new adjuvanted vaccination in development, now approved for adults in the United States for adults, which would reduce the time for series completion from a six month 3-dose series to a one month 2-dose series.[1][9][10] This development would carry the promise to reduce some of the burdens on patients, physician offices, and pharmacies of administering the vaccine series as well as increase vaccination rates.[1][9][10]