22.07.2013 Views

The Australian Immunisation Handbook 10th Edition 2013

The Australian Immunisation Handbook 10th Edition 2013

The Australian Immunisation Handbook 10th Edition 2013

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

3.3.4 Vaccination of recent recipients of normal human<br />

immunoglobulin and other blood products<br />

<strong>The</strong> immune response to live parenteral viral vaccines (with the exception<br />

of yellow fever and zoster vaccine) may be inhibited by normal human<br />

immunoglobulin (NHIG). <strong>The</strong> interval recommended is dependent on the type<br />

and half-life of the immunoglobulin administered (see Table 3.3.6 Recommended<br />

intervals between either immunoglobulins or blood products and MMR, MMRV or<br />

varicella vaccination).<br />

Rotavirus vaccine may be administered at any time before or after, or<br />

concurrently with, any blood product, including antibody-containing products,<br />

following the routinely recommended schedule for rotavirus vaccine among<br />

infants who are eligible for vaccination (see 4.17 Rotavirus). Minimal data are<br />

available on the impact of blood products on the immune response to the vaccine<br />

in these infants. Completing the full rotavirus vaccine series will optimise<br />

protection. 162<br />

Zoster vaccine can be given at any time before or after administration of<br />

immunoglobulin, or any antibody-containing blood product, because those<br />

for whom it is registered (persons ≥50 years of age) are assumed to have had<br />

a previous VZV infection and, therefore, already have serum antibody levels<br />

comparable to those found in blood products (see 4.24 Zoster).<br />

In persons with agammaglobulinaemia who are receiving monthly NHIG,<br />

the use of live vaccines is not recommended as the immune response may be<br />

inhibited. In addition, these people will have sufficient circulating antibody<br />

(e.g. measles, varicella) from the NHIG to protect them in the case of exposure.<br />

Inactivated vaccines are recommended as per the routine schedule; the response<br />

may be suboptimal, but these vaccines are safe to administer.<br />

Persons, who have received a blood transfusion, including mass blood<br />

transfusions, do not require any past vaccinations to be repeated. However,<br />

following the receipt of any blood product, including plasma or platelets, an<br />

interval of 3 to 11 months should elapse, dependent on the blood product<br />

transfused, before vaccination with an MMR, MMRV or varicella vaccine (see<br />

Table 3.3.6 Recommended intervals between either immunoglobulins or blood products<br />

and MMR, MMRV or varicella vaccination). An interval is suggested because there<br />

may be low levels of antibodies present in the blood product that may impair the<br />

immune response to the live vaccine.<br />

166 <strong>The</strong> <strong>Australian</strong> <strong>Immunisation</strong> <strong>Handbook</strong> <strong>10th</strong> edition

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!