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The Australian Immunisation Handbook 10th Edition 2013

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Pre-exposure prophylaxis for rabies virus and other lyssaviruses (including ABLV)<br />

PreP with rabies vaccine is recommended for:<br />

• persons liable to receive bites or scratches from bats (this includes bat<br />

handlers, veterinarians, wildlife officers and others who come into direct<br />

contact with bats) in any country, including Australia<br />

• travellers and expatriates who will be spending time in rabies-enzootic areas;<br />

PreP should occur following a risk assessment that takes into consideration<br />

the likelihood of interaction with animals and access to emergency medical<br />

attention<br />

• persons working with terrestrial animals in rabies-enzootic areas<br />

• research laboratory personnel working with any live lyssaviruses.<br />

Parents travelling with children to rabies-enzootic areas should consider PreP for<br />

younger children, as many children, if bitten by dogs, are often bitten on the face<br />

and hands because they are at an optimal height for such contact.<br />

Serological testing to confirm seroconversion is only necessary in certain<br />

circumstances (see ‘Serological testing following rabies vaccination’ below). 22<br />

PreP simplifies the management of a subsequent exposure because fewer doses<br />

of vaccine are needed and because rabies immunoglobulin (RIG) is not required<br />

(see ‘Post-exposure prophylaxis for rabies virus and other lyssavirus (including<br />

ABLV) exposures’ below). This is particularly important as RIG (human or<br />

equine) is often difficult to obtain in many developing countries and its safety<br />

may not be guaranteed.<br />

Pre-exposure prophylaxis administered via the intradermal route<br />

Intradermal PreP is not recommended because, although initial antibody titres<br />

may be higher, titres at 14 days are lower and wane more rapidly after ID<br />

administration of rabies vaccine than after either IM or SC administration. <strong>The</strong>re<br />

may also be a slow initial immune response following exposure to rabies virus<br />

in those given ID rabies vaccine. 42-44 For these reasons, it is strongly recommended<br />

that the IM route (IM or SC if HDCV is used) be used for pre-exposure prophylaxis. (See<br />

also 4.16.7 Dosage and administration above.)<br />

However, if ID rabies PreP is considered (using a dose of 0.1 mL on days 0, 7 and<br />

28) it is essential that:<br />

• it is given by vaccine providers with not only expertise in, but also regular<br />

practice of, the ID technique<br />

• it is not administered to anyone who is immunocompromised<br />

• it is not administered to persons taking either chloroquine or other<br />

antimalarials structurally related to chloroquine (e.g. mefloquine), at either<br />

the time of, or within a month following, vaccination45 • any remaining vaccine is discarded at the end of the session during which the<br />

vial is opened (8 hours)<br />

PART 4 VACCINE-PREVENTABLE DISEASES 359<br />

4.16 RABIES AND OTHER<br />

LYSSAVIRUSES (INCLUDING<br />

AUSTRALIAN BAT LYSSAVIRUS)

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