Abstract

Introduction:Neisseria meningitidis serogroup B is an important infectious agent in developed countries, including Canada. Infants are particularly susceptible to infection with serogroup B because of immature immune systems, pathogen virulence factors and changing serogroup dynamics in the post-vaccination era. Currently, the Ontario provincial government does not include serogroup B in its routine publicly funded meningococcal vaccination program.Case Presentation:A formerly well 14-month-old male presented to a tertiary hospital emergency department with fever, minor respiratory problems, diffuse purpuric rash, distended abdomen, tachycardia, and history of one episode of vomiting and melena each. Meningococcaemia was immediately suspected, and he was treated with ceftriaxone, cefotaxime and vancomycin before transfer to a different acute care facility within 12 h. N. meningitidis serogroup B, sensitive to ceftriaxone and penicillin, was identified in his blood. The patient developed gangrene of the lower legs and underwent bilateral below-knee amputation 8 days post-admission.Conclusion:This instance of meningococcaemia with extensive sequelae is an example of the various serious outcomes of meningococcal infection. It provides persuasive reason for routine publicly funded vaccination against N. meningitidis serogroup B in Ontario.

Highlights

  • Neisseria meningitidis serogroup B is an important infectious agent in developed countries, including Canada

  • N. meningitidis is a global causative agent of paediatric meningitis and septicaemia, and there are *200 cases of invasive meningococcal disease reported per year in Canada (Andrews & Pollard, 2014; Public Health Agency of Canada, 2014)

  • As noted by Dang et al (2012), serogroup B currently causes most cases of invasive meningococcal disease in Ontario, Canada, and infants are at highest risk

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Summary

Introduction

Neisseria meningitidis is a Gram-negative diplococcus and obligate human pathogen of which there are 12 serogroups, but only six (A, B, C, W-135, X and Y) produce high morbidity and mortality (Pace & Pollard, 2012; Stephens & Greenwood, 2007). Since the overall number of cases of invasive meningococcal disease has decreased with the widespread administering of serogroup A, C, Y and W-135 vaccines as of 2009, the proportion attributable to serogroup B has increased in Canada to *70 % in children younger than 5 years old (Salvadori & Bortolussi, 2011). This is part of a global trend currently observed in developed nations with publicly funded immunization programs (Gounder et al, 2015; Khatami & Pollard, 2010).

Conclusion
Eton and others
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