Hepatitis B Vaccine

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Continuing Education Activity

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

Objectives:

  • Review the mechanism of action of the hepatitis B vaccine.
  • Describe the administration regimens of the hepatitis B vaccine.
  • Explain the monitoring for patients receiving the hepatitis B vaccine, including any toxicity.
  • Outline the importance of improving care coordination amongst the healthcare team to enhance care delivery 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] The 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 first hepatitis B vaccine received FDA approval for use in the United States in 1981, with a recombinant version coming to market in 1986 that replaced the original blood-derived vaccine.[3] 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 any of the following[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 non-infectious subunit of the virus, which leads to an active immunity. Antibodies produced by vaccination target 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.[4]

It is generally accepted that the hepatitis B vaccine confers lifelong protection; originally, it was thought to only last around eight years, but more recent research has confirmed ongoing immunity for at least 25 years in those individuals who demonstrated a good immune response from the vaccine series.[5][6] 

Patients who fail to develop a good response from the vaccine tend to be over 40 years of age, obese, have celiac disease, smoke tobacco, or misuse alcohol. This last group will especially be affected if they have progressed to liver disease.[7][8] 

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][4]

After completing the three vaccination series, patients may receive a blood test after one to four months to determine the immune response, which is defined as an anti-hepatitis B surface antigen (anti-Hbs) antibody level exceeding 100mIU/mL. An antibody response falling between 10 and 100 mIU/mL demonstrates an inadequate response; these patients should get a single booster shot, but do not require a retest. Responses below 10 mIU/mL require additional testing to check for prior hepatitis B infection, and these patients should receive another three-dose regimen with testing again at the one to four-month mark. Continued failed response warrants may require more aggressive interventions, including intradermal administration, high-dose vaccine, or double dosing of combination hepatitis A and hepatitis B vaccine. Should this fail, the patient will need hepatitis B immunoglobulin upon any exposure to the hepatitis B virus.[8][9][10]

Adverse Effects

Research has demonstrated the hepatitis B vaccine to be safe for all age groups.[11] 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%).[12] These effects occurred at similar rates with persons receiving a placebo.[12] 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.[12]

Contraindications

Hepatitis B vaccine is contraindicated in individuals with a history of hypersensitivity to any components of the vaccine or a yeast hypersensitivity.[12][11] Therefore, 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.[11]

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.[12][13] 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.[14][13] 

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.[14] All persons receiving the vaccine should remain under observation for at least 15 minutes following its administration for syncope or signs of anaphylaxis.[4][12][11]

Toxicity

The vaccine is not known to have any dose-dependent toxicity, especially with newer nanoparticle formulations.[7] 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 significant 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][12][15] 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 available for the team 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][15] The hesitant parent and patient who does not respond to this can pose a challenge in vaccination.[15] 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 (as well as other vaccines) 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][16][17] 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][16][17]


Details

Editor:

Rachana Marathi

Updated:

3/24/2023 2:27:31 PM

References


[1]

Hunter P,Fryhofer SA,Szilagyi PG, Vaccination of Adults in General Medical Practice. Mayo Clinic proceedings. 2020 Jan;     [PubMed PMID: 31902413]


[2]

Schillie S,Vellozzi C,Reingold A,Harris A,Haber P,Ward JW,Nelson NP, Prevention of Hepatitis B Virus Infection in the United States: Recommendations of the Advisory Committee on Immunization Practices. MMWR. Recommendations and reports : Morbidity and mortality weekly report. Recommendations and reports. 2018 Jan 12;     [PubMed PMID: 29939980]


[3]

Hepatitis B vaccines: WHO position paper – July 2017. Releve epidemiologique hebdomadaire. 2017 Jul 7     [PubMed PMID: 28685564]


[4]

Romanò L,Paladini S,Galli C,Raimondo G,Pollicino T,Zanetti AR, Hepatitis B vaccination. Human vaccines     [PubMed PMID: 25483515]


[5]

Petersen KM,Bulkow LR,McMahon BJ,Zanis C,Getty M,Peters H,Parkinson AJ, Duration of hepatitis B immunity in low risk children receiving hepatitis B vaccinations from birth. The Pediatric infectious disease journal. 2004 Jul     [PubMed PMID: 15247604]


[6]

Gabbuti A,Romanò L,Blanc P,Meacci F,Amendola A,Mele A,Mazzotta F,Zanetti AR, Long-term immunogenicity of hepatitis B vaccination in a cohort of Italian healthy adolescents. Vaccine. 2007 Apr 20     [PubMed PMID: 17291637]


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S KRN,Nishanth AN,R S AB,Nivedh K,Syed NH,R RS, Hepatitis B-surface antigen (HBsAg) vaccine fabricated chitosan-polyethylene glycol nanocomposite (HBsAg-CS-PEG- NC) preparation, immunogenicity, controlled release pattern, biocompatibility or non-target toxicity. International journal of biological macromolecules. 2020 Feb 1;     [PubMed PMID: 31669465]


[8]

Filippelli M,Lionetti E,Gennaro A,Lanzafame A,Arrigo T,Salpietro C,La Rosa M,Leonardi S, Hepatitis B vaccine by intradermal route in non responder patients: an update. World journal of gastroenterology. 2014 Aug 14;     [PubMed PMID: 25132754]


[9]

Cardell K,Akerlind B,Sällberg M,Frydén A, Excellent response rate to a double dose of the combined hepatitis A and B vaccine in previous nonresponders to hepatitis B vaccine. The Journal of infectious diseases. 2008 Aug 1     [PubMed PMID: 18544037]


[10]

Levitz RE,Cooper BW,Regan HC, Immunization with high-dose intradermal recombinant hepatitis B vaccine in healthcare workers who failed to respond to intramuscular vaccination. Infection control and hospital epidemiology. 1995 Feb     [PubMed PMID: 7759824]


[11]

O'Leary ST,Maldonado YA,Byington CL, Update From the Advisory Committee on Immunization Practices. Journal of the Pediatric Infectious Diseases Society. 2017 Sep 1;     [PubMed PMID: 28903515]


[12]

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[13]

O'leary ST, Maldonado YA, Kimberlin DW. Update From the Advisory Committee on Immunization Practices. Journal of the Pediatric Infectious Diseases Society. 2019 Dec 27:8(6):495-500. doi: 10.1093/jpids/piz058. Epub     [PubMed PMID: 31589289]


[14]

Schillie S,Murphy TV,Sawyer M,Ly K,Hughes E,Jiles R,de Perio MA,Reilly M,Byrd K,Ward JW, CDC guidance for evaluating health-care personnel for hepatitis B virus protection and for administering postexposure management. MMWR. Recommendations and reports : Morbidity and mortality weekly report. Recommendations and reports. 2013 Dec 20;     [PubMed PMID: 24352112]


[15]

Constable C,Caplan A, Comparison of the implementation of human papillomavirus and hepatitis B vaccination programs in the United States: Implications for future vaccines. Vaccine. 2019 Dec 13;     [PubMed PMID: 31843271]


[16]

Splawn LM,Bailey CA,Medina JP,Cho JC, Heplisav-B vaccination for the prevention of hepatitis B virus infection in adults in the United States. Drugs of today (Barcelona, Spain : 1998). 2018 Jul;     [PubMed PMID: 30090877]


[17]

Hyer R,McGuire DK,Xing B,Jackson S,Janssen R, Safety of a two-dose investigational hepatitis B vaccine, HBsAg-1018, using a toll-like receptor 9 agonist adjuvant in adults. Vaccine. 2018 May 3;     [PubMed PMID: 29628151]