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The Australian Immunisation Handbook 10th Edition 2013

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Persons with autoimmune diseases and other chronic conditions<br />

Persons with autoimmune conditions, such as systemic lupus erythematosus<br />

(SLE), rheumatoid arthritis (RA) and multiple sclerosis (MS), are at higher<br />

risk of infections, including vaccine-preventable diseases, with the associated<br />

potential morbidity and mortality from infection. <strong>The</strong>y are also at risk of<br />

infection due to treatment with immunosuppressive agents such as bDMARDs<br />

and targeted biological therapies. 148 Some diseases can be reactivated during<br />

therapy, so screening for infections such as hepatitis B and tuberculosis should be<br />

undertaken prior to vaccination. 149,150<br />

Overall, theoretical concerns that vaccines exacerbate or cause autoimmune<br />

diseases such as rheumatoid arthritis, type 1 diabetes and multiple sclerosis<br />

have not been substantiated, with sporadic case reports not verified by larger<br />

epidemiological studies. 151-154 However, persons with a history of Guillain-Barré<br />

syndrome (GBS) have an increased likelihood in general of developing GBS<br />

again, and the chance of them coincidentally developing the syndrome following<br />

influenza vaccination may be higher than in persons with no history of GBS.<br />

A small increased risk of GBS was associated historically with one influenza<br />

vaccine in the United States in 1976, but, since then, close surveillance has shown<br />

that GBS has occurred at a very low rate of up to 1 in 1 million doses of influenza<br />

vaccine, if at all. 155<br />

In persons with autoimmune diseases and other chronic conditions,<br />

there is potential for reduced immunogenicity of vaccines, due to both<br />

immunosuppressive therapies and the underlying disease. 156-158 <strong>The</strong> duration<br />

of immunocompromise may be prolonged and caution must be taken when<br />

considering live vaccines. Inactivated vaccines are recommended, to optimise<br />

protection despite the potential for reduced immunogenicity in some people.<br />

Clinical and laboratory measures of disease activity, and the choice, duration<br />

and dose of immunosuppressive therapies, do not always predict who will<br />

respond poorly to vaccination. 157,159,160 In some instances, due to ongoing risk<br />

of disease, additional vaccine doses may be required, such as pneumococcal<br />

vaccine. Inactivated vaccines such as HPV and dTpa can be administered to<br />

immunocompromised persons. Annual influenza vaccine is also important in<br />

this population and should be administered annually (2 doses in the first year,<br />

1 annually thereafter).<br />

Hypopituitarism is not a contraindication to vaccination if the person is only<br />

receiving physiological corticosteroid replacement, as this is not considered<br />

immunosuppressive. If the person has been unwell and is on high-dose<br />

corticosteroids for more than 1 week, the use of live attenuated vaccines should<br />

be delayed for a minimum of 1 month.<br />

Persons with metabolic diseases should be vaccinated using the routine schedule,<br />

as vaccinations are generally considered safe in these persons. 161 Influenza and<br />

pneumococcal vaccines are recommended for those with metabolic disease. Any<br />

individual concerns should be discussed with the treating metabolic physician.<br />

PART 3 VACCINATION FOR SPECIAL RISK GROUPS 165<br />

3.3 GROUPS WITH SPECIAL<br />

VACCINATION REQUIREMENTS

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