What are the rates of Meningococcal (Meningitis) B disease in Australia?

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Last updated: October 15, 2025View editorial policy

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Meningococcal B Disease Rates in Australia

In Australia, meningococcal serogroup B (MenB) disease has been the predominant cause of invasive meningococcal disease (IMD), accounting for 82% of cases in South Australia compared to the national average of 36% as of 2016. 1

Current Epidemiology

  • The incidence of meningococcal B disease in Australia has declined progressively from 1.52 cases per 100,000 population in 2001 to 0.47 per 100,000 in 2015 2
  • During 2006-2015, MenB accounted for 81% of IMD cases with a known serogroup in Australia 2
  • The highest incidence rates of MenB disease in Australia are found in:
    • Infants under 12 months of age: 11.1 per 100,000 population 2
    • Children aged 1-4 years: 2.82 per 100,000 population 2
    • Adolescents aged 15-19 years: 2.40 per 100,000 population 2
  • Among infants under 2 years with MenB disease, 43% were under 7 months and 69% under 12 months of age 2

Population Disparities

  • Indigenous Australians have significantly higher rates of MenB disease compared to non-Indigenous Australians during 2006-2015 (incidence rate ratio [IRR], 3.8; 95% CI, 3.3-4.5) 2
  • In South Australia specifically, the mean rate of MenB disease was 2.8 per 100,000 population during 2000-2017 1
  • Some regions, like South Western Sydney, have historically shown higher incidence than the national rate 3

Recent Vaccination Programs and Impact

  • South Australia implemented the first statewide MenB vaccine program for infants, children, and adolescents due to the high burden of MenB disease in that state 1
  • The South Australian program provides 4CMenB (Bexsero) to children aged six weeks to 12 months, and young people aged 15 to 17 years 4
  • A statewide cluster randomized trial in South Australia showed that vaccinating adolescents with 4CMenB was associated with a 71% reduction (95% CI, 15%-90%) in group B meningococcal disease 5
  • From 2017-2019, serogroup B IMD cases in 16-19 year-olds in South Australia reduced significantly below expected numbers following the vaccination program 5

Risk Groups

  • Based on disease incidence, priority at-risk groups for MenB vaccination in Australia include:
    • All children between 2 months and 5 years of age 2
    • Indigenous children under 10 years of age 2
    • All adolescents aged 15-19 years 2

Vaccine Availability and Safety

  • Bexsero (4CMenB) is licensed in Australia for protection against meningococcal serogroup B disease 6
  • Safety surveillance data from South Australia's program (2018-2022) showed a reporting rate of 69.9 adverse events following immunization per 100,000 doses, with most being known, common, non-serious events (85% of reports) 4
  • The most frequently reported non-serious adverse events were rash (14%), injection site reaction (14%), nausea/vomiting/diarrhea (11%), and fever (11%) 4

Historical Context

  • There has been a sustained increase in the incidence of meningococcal disease throughout Australia since 1987 3
  • In some regions like South Western Sydney, serogroup C was historically the predominant organism, which is unusual compared to the national pattern where serogroup B organisms predominated 3
  • The introduction of meningococcal C vaccine in 2003 led to significant reductions in MenC disease 2

Given the marked variation in meningococcal disease trends over time, continued surveillance of current epidemiologic data remains essential for guiding vaccination policies in Australia 2.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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