The Australian Immunisation Handbook 10th Edition 2013

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Vaccine component* Vaccine brand † Antigen Polymyxin Fluvax Influenza Infanrix hexa Diphtheria-tetanus-acellular pertussishepatitis B-inactivated poliomyelitis- Haemophilus influenzae type b (DTPa-hepB- IPV-Hib) Infanrix IPV Diphtheria-tetanus-acellular pertussisinactivated poliomyelitis (DTPa-IPV) Quadracel Diphtheria-tetanus-acellular pertussisinactivated poliomyelitis (DTPa-IPV) Polysorbate or Agrippal Influenza sorbitol Boostrix Diphtheria-tetanus-acellular pertussis (dTpa) reduced antigen Fluarix Influenza Gardasil Human papillomavirus (HPV) Havrix Junior Hepatitis A (HAV) paediatric Infanrix hexa Diphtheria-tetanus-acellular pertussishepatitis B-inactivated poliomyelitis- Haemophilus influenzae type b (DTPa-hepB- IPV-Hib) Infanrix IPV Diphtheria-tetanus-acellular pertussisinactivated poliomyelitis (DTPa-IPV) Influvac Influenza Prevenar 13 13-valent pneumococcal conjugate (13vPCV) Priorix Measles-mumps-rubella (MMR) Priorix-tetra Measles, mumps, rubella and varicella (MMRV) ProQuad Measles-mumps-rubella-varicella (MMRV) Quadracel Diphtheria-tetanus-acellular pertussisinactivated poliomyelitis (DTPa-IPV) RotaTeq Rotavirus Yeast Engerix-B Hepatitis B (HBV) adult and paediatric Gardasil Human papillomavirus (HPV) H-B-Vax II Hepatitis B (HBV) adult and paediatric Infanrix hexa Diphtheria-tetanus-acellular pertussishepatitis B-inactivated poliomyelitis- Haemophilus influenzae type b (DTPa-hepB- IPV-Hib) * If the person to be vaccinated has had an anaphylactic reaction to any of the vaccine components, administration of that vaccine may be contraindicated. Specialist advice should be sought to identify the component and to review if the person can be vaccinated in future. † Please also refer to Appendix 4 Commonly asked questions about vaccination for more specific information about these various constituents. 472 The Australian Immunisation Handbook 10th edition
APPENDIX 4: COMMONLY ASKED QUESTIONS ABOUT VACCINATION This appendix contains information for providers to refer to when responding to questions and concerns about immunisation. It covers general questions on adult and childhood vaccination, including contraindications and precautions. In addition, a discussion on some of the more recent concerns about vaccination is included, covering issues relating to vaccine safety, vaccine content, immunisation as a possible cause of some illnesses of uncertain origin, and the need for vaccination. This appendix is divided into six sections: • General questions • Questions about contraindication and precautions • Questions about vaccine safety • Questions about vaccine content • Questions about the need for immunisation • Further information about vaccination A.4.1 General questions How does vaccination work? When a healthy person becomes infected with a virus or bacteria (also known as a pathogen), for example, the measles virus, the body recognises the virus as an invader, produces antibodies that eventually destroy the virus, and recovery occurs. If contact with the measles virus occurs again in the future, the body’s immune system ‘remembers’ the measles virus and produces an increase in antibodies to destroy this pathogen. Vaccination is the process that is used to stimulate the body’s immune system in the same way as the real pathogen or disease would, but without causing the symptoms of the disease. Most vaccines provide the body with ‘memory’ so that an individual does not get the disease if exposed to it (see 1.5 Fundamentals of immunisation). Vaccination conveys immunity to diseases by a process called active immunity, which can be achieved by administration of either inactivated (i.e. not live) or live attenuated pathogens or their products. Live vaccines are attenuated, or weakened, by growing the organism through serial culturing (or passaging) steps in various tissue culture media. Inactivation is usually done using heat or formalin (sometimes both). Inactivated vaccines may include the whole pathogen (such as oral cholera vaccine), the toxin produced by the pathogen (such as tetanus and diphtheria vaccines), or specific antigens (such as Haemophilus influenzae type b [Hib], meningococcal and pneumococcal APPENDIX 4 473 APPENDIX 4
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The Australian Immunisation Handboo
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FOREWORD Since 1932, when Governmen
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TABLE OF CONTENTS PART 1 INTRODUCTI
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LIST OF TABLES Table 2.1.1: Pre-vac
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List 4.13.1: Conditions associated
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PREFACE The 10th edition of The Aus
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Secretariat support, Australian Tec
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PART 1 INTRODUCTION TO THE AUSTRALI
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1.2 DEVELOPMENT OF THE 10TH EDITION
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1.3 HOW TO USE THE 10TH EDITION HAN
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1.4 WHAT’S NEW All chapters have
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2.2 Administration of vaccines •
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• The section on vaccination of p
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4.6 Human papillomavirus • HPV va
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• For Aboriginal and Torres Strai
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Part 5 Passive immunisation • Inf
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without the harmful consequences of
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(vaccine failure). Often such infec
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will occur following receipt of a s
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cases, both the doctor issuing the
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Should a child or adolescent refuse
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• check that the correct time int
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Note: Please discuss this informati
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Condition or circumstance of person
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Condition or circumstance of person
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Table 2.1.3: Live attenuated parent
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An online ‘catch-up calculator’
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Use of serological testing to guide
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• For some vaccines, catch-up vac
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Figure 2.1.1: Catch-up worksheet fo
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Vaccine Minimum age for 1st dose in
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Table 2.1.6: Number of vaccine dose
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Catch-up guidelines for individual
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If 13vPCV is not available, and 10v
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Previous vaccination history 2 prev
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PART 2 VACCINATION PROCEDURES 57 Ta
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PART 2 VACCINATION PROCEDURES 59 Ta
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Catch-up schedules for persons ≥1
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For additional details on these rec
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2.2 ADMINISTRATION OF VACCINES 2.2.
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• Never freeze a vaccine after it
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PART 2 VACCINATION PROCEDURES 69 In
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2.2.5 Vaccine injection techniques
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Interruption to a vaccination If th
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2.2.7 Positioning for vaccination I
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Children ≥12 months of age Cuddle
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2.2.8 Identifying the injection sit
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• Place the palm over the greater
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2.2.9 Administering multiple vaccin
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2.3 POST-VACCINATION 2.3.1 Immediat
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Management of an immediate adverse
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Management of anaphylaxis Rapid IM
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Autoinjectors are generally not app
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Australia. 16 This vaccine is no lo
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Any serious or unexpected adverse e
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Consumers and immunisation service
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When relevant, immunisation service
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National Human Papillomavirus Vacci
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Immunisation service providers enro
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PART 3 VACCINATION FOR SPECIAL RISK
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Thus, a vaccine to prevent Hib dise
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3.1.2 Adults Hepatitis B Indigenous
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een low in younger Indigenous adult
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3.2 VACCINATION FOR INTERNATIONAL T
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• vaccination history (including
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departure to allow for the period w
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Selected vaccines based on travel i
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Tick-borne encephalitis Tick-borne
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3.2.5 Vaccinating the traveller wit
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• Travel health and quarantine se
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whether the AEFI is likely to recur
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(see Appendix 1 Contact details for
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avoided, except in situations where
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3.3.3 Vaccination of immunocompromi
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Use of live viral or live bacterial
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Influenza vaccination is recommende
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Haematopoietic stem cell transplant
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Vaccine Months after HSCT Comments
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depending on the number of vaccines
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Persons with functional or anatomic
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Table 3.3.5: Recommendations for va
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Persons with autoimmune diseases an
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Table 3.3.6: Recommended intervals
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3.3.7 Vaccination of persons at occ
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Occupation Vaccine Providers of hom
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against certain vaccine-preventable
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3.3.11 Vaccination of persons who i
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waters. All cases of cholera report
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Children aged 2-6 years Three doses
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4.1.11 Adverse events The inactivat
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4.2.4 Vaccines Diphtheria toxoid is
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• Adacel - Sanofi Pasteur Pty Ltd
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antibodies at an age when waning of
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children aged
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4.3 HAEMOPHILUS INFLUENZAE TYPE B 4
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• Hiberix - GlaxoSmithKline (PRP-
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4.3.7 Recommendations Infants A Hib
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4.3.11 Public health management of
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In recent years, hepatitis A notifi
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Inactivated hepatitis A vaccines ar
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Co-administration with other vaccin
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Recommendations for the use of comb
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4.4.10 Adverse events The most comm
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4.5.3 Epidemiology The prevalence o
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4.5.4 Vaccines Monovalent hepatitis
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For older children and young adults
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Vaccine Age of vaccine recipient Do
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Combination hepatitis A/hepatitis B
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Management of infants born to mothe
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Household or other close (household
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with occult hepatitis B infection.
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immune memory persists and is thoug
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to suggest that a higher proportion
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Table 4.5.3: Post-exposure prophyla
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4.6 HUMAN PAPILLOMAVIRUS 4.6.1 Viro
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women. The prevalence of high-risk
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• Gardasil - CSL Limited/Merck &
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If scheduled doses have been missed
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However, some adult males may gain
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4.6.9 Contraindications The only ab
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4.7 INFLUENZA 4.7.1 Virology The in
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Figure 4.7.1: Influenza notificatio
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Always check annual seasonal influe
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7.5 µg of viral haemagglutinin (in
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Table 4.7.1: Recommended doses of i
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• Chronic respiratory conditions,
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Residents of residential aged care
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influenza vaccine prior to administ
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4.8 JAPANESE ENCEPHALITIS 4.8.1 Vir
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28 days following vaccination with
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When using JEspect in children aged
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4.8.8 Pregnancy and breastfeeding I
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4.9 MEASLES 4.9.1 Virology Measles
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4.9.4 Vaccines Monovalent measles v
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4.9.6 Dosage and administration The
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Table 4.9.1: Recommendations for me
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increase in adverse events from vac
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Immunoglobulin or blood product adm
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approximately 5%. 2,25 There is als
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Table 4.9.2: Post-exposure prophyla
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4.10 MENINGOCOCCAL DISEASE 4.10.1 B
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4.10.4 Vaccines There are different
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Polysaccharide vaccines Quadrivalen
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Interchangeability of meningococcal
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• Children (aged ≥9 months) and
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Appendix 1 Contact details for Aust
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4.11 MUMPS 4.11.1 Virology Mumps is
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Trivalent measles-mumps-rubella (MM
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4.11.7 Recommendations Infants aged
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Vaccination with other live attenua
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acquired from healthcare workers. 1
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demonstrated a more rapid decline,
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• Boostrix-IPV - GlaxoSmithKline
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in the previous 10 years. 19,45 Adu
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(see ‘Women who are planning preg
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an HHE. An HHE may last from a few
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The product information for Quadrac
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4.13 PNEUMOCOCCAL DISEASE 4.13.1 Ba
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non-Indigenous children (88%). 19,2
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10-valent pneumococcal conjugate va
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lesser antibody responses to 2nd or
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Table 4.13.1: Recommendations for p
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Category B: Conditions associated w
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Children aged >5 years to 15 years)
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Non-Indigenous adults A single dose
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Adults who have a condition listed
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4.13.11 Adverse events 10-valent pn
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5 years with a condition(s) associa
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virtually eradicated in India, but
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formaldehyde, glutaraldehyde, polys
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4.14.8 Pregnancy and breastfeeding
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4.15 Q FEVER 4.15.1 Bacteriology Q
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4.15.4 Vaccine • Q-Vax - CSL Limi
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individuals, which can be accessed
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Refer to 3.3 Groups with special va
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4.16 RABIES AND OTHER LYSSAVIRUSES
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4.16.4 Rabies vaccines • Mérieux
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of an even more accelerated schedul
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Pre-exposure prophylaxis for rabies
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The relevant state/territory health
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Although data are limited on the ef
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Table 4.16.2: Post-exposure prophyl
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Figure 4.16.2: Post-exposure prophy
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Figure 4.16.3: Booster algorithm fo
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allergic reaction occurs following
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age group11,12 and affecting 3.8% o
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of age, the risk of IS was increase
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Interchangeability of rotavirus vac
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gestational age; median 34 weeks) w
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Infants living in households with p
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4.17.12 Variations from product inf
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2003, rubella notifications in Aust
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zoster virus [Oka strain]). Lyophil
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children
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A number of commercial assays for t
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Germany indicates that no case of v
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case. Seronegative women of child-b
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4.19 TETANUS 4.19.1 Bacteriology Te
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Formulations for children aged
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4.19.5 Transport, storage and handl
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foreign bodies (especially wood spl
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studies indicate that the adverse r
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The product information for Adacel
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of MDR-TB cases identified has incr
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BCG vaccination procedures BCG vacc
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Occupational groups There is some e
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4.20.13 Variations from product inf
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In developed countries, typhoid fev
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A 4th capsule taken on day 7 has be
Page 435 and 436: 4.21.8 Pregnancy and breastfeeding
Page 437 and 438: 4.22 VARICELLA 4.22.1 Virology Vari
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Page 447 and 448: immunoglobulin and other blood prod
Page 449 and 450: eported in a 9-year follow-up of 70
Page 451 and 452: high-dose intravenous NHIG are like
Page 453 and 454: 4.23 YELLOW FEVER 4.23.1 Virology Y
Page 455 and 456: Co-administration with other vaccin
Page 457 and 458: 4.23.8 Pregnancy and breastfeeding
Page 459 and 460: Vaccine-associated neurotropic adve
Page 461 and 462: 1000 cases per 100 000 population i
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Page 465 and 466: diagnosis. In addition, the risk of
Page 467 and 468: Laboratory testing to check for an
Page 469 and 470: 4.24.12 Variations from product inf
Page 471 and 472: the immunoglobulin preparations con
Page 473 and 474: Prevention of measles Measles vacci
Page 475 and 476: who are being treated with immunosu
Page 477 and 478: limb with a separate syringe, and a
Page 479 and 480: APPENDIX 1: CONTACT DETAILS FOR AUS
Page 481 and 482: APPENDIX 2: LITERATURE SEARCH STRAT
Page 483 and 484: APPENDIX 3: COMPONENTS OF VACCINES
Page 485: Vaccine component* Vaccine brand
Page 489 and 490: When should preterm infants be vacc
Page 491 and 492: If a parent decides not to have a c
Page 493 and 494: Should vaccines be given to persons
Page 495 and 496: eason not to vaccinate. Asthma, ecz
Page 497 and 498: Does MMR vaccine cause inflammatory
Page 499 and 500: (either alone or in combination) fo
Page 501 and 502: A4.5 Questions about the need for i
Page 503 and 504: APPENDIX 5: GLOSSARY OF TECHNICAL T
Page 505 and 506: Enzootic enzootic infections are pr
Page 507 and 508: Rotavirus a virus that is a common
Page 509 and 510: APPENDIX 6: COMMONLY USED ABBREVIAT
Page 511 and 512: OPV oral poliomyelitis vaccine PCEC
Page 513 and 514: Year Vaccine 2003 Varicella 2003 Me
Page 515 and 516: identifying the injection site, 79-
Page 517 and 518: Australian Capital Territory advers
Page 519 and 520: and travellers, 119 vaccines, 177-1
Page 521 and 522: abies and other lyssaviruses (inclu
Page 523 and 524: HPV Vaccination Program, 234 human
Page 525 and 526: interferon-gamma release assays (IG
Page 527 and 528: mercury, in vaccines. see thiomersa
Page 529 and 530: Northern Territory ACIR reporting,
Page 531 and 532: and Haemophilus influenzae type b (
Page 533 and 534: espiratory syncytial virus monoclon
Page 535 and 536: Therapeutic Goods Administration (T
Page 537 and 538:
varicella-zoster immunoglobulin, 45
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INDEX 525 INDEX
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