Literature DB >> 12921484

The place of accelerated schedules for hepatitis A and B vaccinations.

Jane Zuckerman1.   

Abstract

The availability of accelerated schedules of vaccination, as well as the development of combination vaccines, has enhanced the methods of protection against infectious disease, in particular that of hepatitis A and B viruses. The benefits of using accelerated schedules include: (i) enhanced adherence to and subsequent completion of vaccine courses; (ii) convenience for the recipient of the vaccine; (iii) reduced administration costs of providing the vaccine; and, most importantly, (iv) the ability to provide protection against these serious infections to those who will be imminently exposed to the risk and so require protection as quickly as possible. Active immunisation against both hepatitis A and B viruses has only been recognised within the last 20 years. During this time clinical studies have demonstrated the safety and efficacy of administering the monovalent hepatitis B vaccine by way of accelerated schedules. There are now several accelerated schedules of administration of hepatitis B vaccine which can be tailored to the needs of the individual at risk of exposure to infection. One such schedule allows the primary course to be administered within a period of 1 month. This schedule of day 0, 7 and 21, with a booster at 12 months, is licensed for use with the recombinant hepatitis B vaccine Engerix B and results in a seroprotection rate of 65% at day 28 which increases to 99% at month 13. In more recent years, the development of a multivalent or combination vaccine against hepatitis A and B (Twinrix) has been a welcome advance in the protection against viral hepatitis, and has been of particular benefit to those who are at risk of infection with both viruses. The advantages of accelerated schedules have also been recognised with this combination vaccine. The primary course may be administered within a period of 1 month so providing protection for those at risk and, in particular, the last minute traveller.

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Year:  2003        PMID: 12921484     DOI: 10.2165/00003495-200363170-00001

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  25 in total

1.  A prospective, randomized, comparative US trial of a combination hepatitis A and B vaccine (Twinrix) with corresponding monovalent vaccines (Havrix and Engerix-B) in adults.

Authors:  R W Joines; M Blatter; B Abraham; F Xie; N De Clercq; Y Baine; K S Reisinger; A Kuhnen; D L Parenti
Journal:  Vaccine       Date:  2001-09-14       Impact factor: 3.641

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Journal:  Lancet       Date:  1998-05-30       Impact factor: 79.321

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Journal:  Lancet       Date:  2000-02-12       Impact factor: 79.321

4.  Comparative study of the immunogenicity and safety of two doses of recombinant hepatitis B vaccine in healthy adolescents.

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Journal:  J Adolesc Health       Date:  1995-01       Impact factor: 5.012

5.  Antibody responses to Hepatitis A vaccine in healthy adults.

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Journal:  Commun Dis Public Health       Date:  2001-06

6.  Comparative immunogenicity and safety of two dosing schedules of a combined hepatitis A and B vaccine in healthy adolescent volunteers: an open, randomised study.

Authors:  M A Burgess; A J Rodger; S A Waite; F Collard
Journal:  Vaccine       Date:  2001-09-14       Impact factor: 3.641

7.  Immunogenicity and reactogenicity of a combined high dose hepatitis A and hepatitis B vaccine, compared to that of Twinrix in healthy Indian children.

Authors:  Rajkumar C Guptan; Varsha Thakur; Assad Safary; Shiv K Sarin
Journal:  Vaccine       Date:  2002-05-15       Impact factor: 3.641

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Authors:  Jia-Horng Kao; Ding-Shinn Chen
Journal:  Lancet Infect Dis       Date:  2002-07       Impact factor: 25.071

9.  Clinical and immunological investigation of a new combined hepatitis A and hepatitis B vaccine.

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Journal:  Vaccine       Date:  1995       Impact factor: 3.641

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  4 in total

Review 1.  Schedules for hepatitis B vaccination of risk groups: balancing immunogenicity and compliance.

Authors:  K Van Herck; E Leuridan; P Van Damme
Journal:  Sex Transm Infect       Date:  2007-10       Impact factor: 3.519

Review 2.  Old and new adjuvants for hepatitis B vaccines.

Authors:  Geert Leroux-Roels
Journal:  Med Microbiol Immunol       Date:  2014-12-19       Impact factor: 3.402

Review 3.  Combined hepatitis A and B vaccines: a review of their immunogenicity and tolerability.

Authors:  David L Murdoch; Karen Goa; David P Figgitt
Journal:  Drugs       Date:  2003       Impact factor: 9.546

4.  Feasibility of completing an accelerated vaccine series for homeless adults.

Authors:  A M Nyamathi; K Sinha; S Saab; M Marfisee; B Greengold; B Leake; D Tyler
Journal:  J Viral Hepat       Date:  2009-02-24       Impact factor: 3.728

  4 in total

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