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Meningococcal meningitis is an acute bacterial disease characterised by sudden onset of fever, intense headache, vomiting and a stiff neck. A skin rash appears in the later stages of the disease and signifies severe illness. Although the disease is treatable with antibiotics, sufferers may become very sick or even die within hours of onset if not diagnosed promptly and correctly. The disease is transmitted from person-to-person by respiratory droplets i.e. coughing, sneezing etc. Extensive travel in crowded conditions or extended contact with the local population in crowded places are among the main risk factors.
Meningococcal Meningitis occurs in all countries. In sub-Saharan Africa, epidemics of serogroup A meningococcal disease occur frequently during the dry season (December through June) particularly in the savannah areas extending from Mali eastward to Ethiopia, a region known as the ‘meningitis belt’. Epidemics due to serogroups A and/or C have also occurred in areas further south in Africa (Tanzania, Burundi, Angola) as well as in parts of Asia, in particular northern India, Nepal and Mongolia, again during the dry season (November to May). A complex range of risk factors cause epidemics.
The risk to travellers is generally low. Vaccination is recommended for travel to the ‘meningitis belt’ during the dry season, for travel to areas with an active epidemic, or for prolonged travel when extensive contact with the local population in endemic areas is expected.
NOTE - Meningococcal meningitis vaccination is mandatory for all travellers over three months of age making the pilgrimage to Saudi Arabia for the Hajj.
Usually infrequent and mild:
As with all vaccines, there is a small risk of allergic reaction.
In Australia and other developed nations meningitis is mainly found in the form of Neisseria meningitidis serogroup C.
The Conjugate C vaccine provides long-term immunity against this form of the disease; it provides active immunisation of children from the age of 6 weeks, and in adolescents and adults.
Infants - Data indicates that immunity was achieved in 91% of infants after 1 dose and 98-100% of infants one month after the third dose. There are currently no recommendations for boosting.
Adults - 99-100% of adults had an adequate response after a single dose of vaccine.