期刊论文详细信息
BMC Infectious Diseases
Epidemiology of serogroup B invasive meningococcal disease in Ontario, Canada, 2000 to 2010
Shelley L Deeks2  Raymond S W Tsang3  Karen Johnson1  Natasha S Crowcroft4  Prasad Rawte1  Sarah Wilson2  Frances B Jamieson4  Vica Dang2 
[1]Public Health Ontario, Toronto, ON, Canada
[2]Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canada
[3]National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, MB, Canada
[4]Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada
关键词: Canada;    Ontario;    Surveillance;    Epidemiology;    Serogroup B;    Neisseria meningitidis;    Invasive meningococcal disease;   
Others  :  1159706
DOI  :  10.1186/1471-2334-12-202
 received in 2012-02-14, accepted in 2012-08-02,  发布年份 2012
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【 摘 要 】

Background

Invasive meningococcal disease (IMD) caused by serogroup B is the last major serogroup in Canada to become vaccine-preventable. The anticipated availability of vaccines targeting this serogroup prompted an assessment of the epidemiology of serogroup B disease in Ontario, Canada.

Methods

We retrieved information on confirmed IMD cases reported to Ontario’s reportable disease database between January 1, 2000 and December 31, 2010 and probabilistically-linked these cases to Public Health Ontario Laboratory records. Rates were calculated with denominator data obtained from Statistics Canada. We calculated a crude number needed to vaccinate using the inverse of the infant (<1 year) age-specific incidence multiplied by expected vaccine efficacies between 70% and 80%, and assuming only direct protection (no herd effects).

Results

A total of 259 serogroup B IMD cases were identified in Ontario over the 11-year period. Serogroup B was the most common cause of IMD. Incidence ranged from 0.11 to 0.27/100,000/year, and fluctuated over time. Cases ranged in age from 13 days to 101 years; 21.4% occurred in infants, of which 72.7% were <6 months. Infants had the highest incidence (3.70/100,000). Case-fatality ratio was 10.7% overall. If we assume that all infant cases would be preventable by vaccination, we would need to vaccinate between 33,784 and 38,610 infants to prevent one case of disease.

Conclusions

Although rare, the proportion of IMD caused by serogroup B has increased and currently causes most IMD in Ontario, with infants having the highest risk of disease. Although serogroup B meningococcal vaccines are highly anticipated, our findings suggest that decisions regarding publicly funding serogroup B meningococcal vaccines will be difficult and may not be based on disease burden alone.

【 授权许可】

   
2012 Dang et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Brown EM, Fisman DN, Drews S, Doman S, Rawte P, Brown S, Jamieson F: Epidemiology of invasive meningococcal disease with decreased susceptibility to penicillin in Ontario, Canada, 2000 to 2006. Antimicrob Agents Chemother 2010, 54(3):1016-21.
  • [2]Tsang RSW, Squires SG, Tam TWS: Characterization of Neisseria meningitidis strains isolated from invasive meningococcal disease cases in Canada in 2001. Can J Microbiol 2003, 49:633-8.
  • [3]Rosenstein NE, Perkins BA, Stephens DS, Popovic T, Hughes JM: Meningococcal disease. N Engl J Med 2001, 344:1378-88.
  • [4]Navarro C, Deeks SL, Medaglia A, Tsang RSW: Enhanced surveillance of invasive meningococcal disease in Canada: 1 January, 2004, through 31 Dec, 2005. Can Commun Dis Rep 2007, 33(10):1-15.
  • [5]Public Health Agency of Canada: Guidelines for the Prevention and Control of Meningococcal Disease. Can Commun Dis Rep 2005, 31(S1):1-20.
  • [6]Vedros NA: Development of meningococcal serogroups. In Evolution of Meningococcal Disease. Volume 2. Boca Raton, Florida: CRC Press; 1987:33-7.
  • [7]Law DKS, Lorange M, Ringuette L, Dion R, Giguere M, Henderson AM, Stoltz J, Zollinger WD, De Wals P, Tsang RSW: Invasive meningococcal disease in Québec, Canada, due to an emerging clone of ST-269 serogroup B meningococci with serotype antigen 17 and serosubtype antigen P1.19 (B:17:P1.19). J Clin Microbiol 2006, 44(8):2743-9.
  • [8]National Advisory Committee on Immunization (NACI): An update on the invasive meningococcal disease and meningococcal vaccine conjugate recommendations. An Advisory Committee Statement (ACS). Can Commun Dis Rep 2009, 35(ACS-3):1-40.
  • [9]Perrett KR, Pollard AJ: Towards an improved serogroup B Neisseria meningitidis vaccine. Expert Opin Biol Ther 2005, 5(12):1611-25.
  • [10]Wenger JD, Serogroup B: meningococcal disease: new outbreaks, new strategies. JAMA 1999, 281(16):1541-3.
  • [11]Association of Public Health Epidemiologists in Ontario: 10 Integrated Public Health Information System (iPHIS). [http://www.apheo.ca/index.php?pid=187 webcite]
  • [12]Ministry of Health & Long-Term Care: Appendix B: Provincial Case Definitions for Reportable Disease: Meningococcal disease, invasive. Ontario Public Health Standards: Infectious Diseases Protocol; 2009. [http://www.health.gov.on.ca/english/providers/program/pubhealth/oph_standards/ophs/infdispro.html webcite]
  • [13]Ontario Ministry of Health & Long-Term Care: Appendix 2: iPHIS Manual. Toronto: Public Health Division; 2005.
  • [14]Laupacis A, Sackett DL, Roberts RS: An assessment of clinically useful measures of the consequences of treatment. N Engl J Med 1988, 318:1728-33.
  • [15]Gossger N, Snape MD, Yu LM, Finn A, Bona G, Esposito S, Principi N, Diez-Diez-Domingo J, Sokal E, Becker B, Kieninger D, Prymula R, Dull P, Ypma E, Toneatto D, Kimura A, Pollard AJ: Immunogenicity and tolerability of recombinant serogroup B meningococcal vaccine administered with or without routine infant vaccinations according to different immunization schedules. JAMA 2012, 306(6):573-82.
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