 |
 |

Serogroup Y Meningococcal Disease in Chicago, 1991-1997
Judith A. Racoosin, MD, MPH;
Cynthia G. Whitney, MD, MPH;
Craig S. Conover, MD, MPH;
Pamela S. Diaz, MD
JAMA. 1998;280:2094-2098.
Context. In 1994, surveillance by the Chicago Department of Public Health detected a growing trend in the proportion of invasive meningococcal infections caused by serogroup Y.
Objective. To examine the emergence of serogroup Y meningococcal disease and compare its clinical characteristics with those of other meningococcal serogroups.
Design. Population-based retrospective review of surveillance records; medical record review and cohort analysis of serogroup Y vs nonserogroup Y case patients.
Setting. Chicago, Ill.
Participants. City residents with Neisseria meningitidis isolated from a normally sterile site from January 1, 1991, through December 31, 1997; cohort analysis included those identified through March 31, 1996.
Main Outcome Measures. Serogroup-specific incidence, demographics, and clinical outcomes.
Results. We identified 214 case patients; 53 (25%) had serogroup Y. The attack rate of serogroup Y meningococcal disease increased from 0.04 cases per 100,000 in 1991 to a peak of 0.82 cases per 100,000 in 1995 and subsequently decreased to 0.26 cases per 100,000 and 0.34 cases per 100,000 in 1996 and 1997, respectively. Compared with patients infected by other serogroups, patients with serogroup Y were older (median age, 16 years vs 1 year; P = .001) and more likely to have a chronic underlying illness (prevalence ratio, 2.3; 95% confidence interval, 1.2-4.4). Outcome did not differ significantly between the 2 groups. Multilocus enzyme electrophoresis typing of isolates from 19 case patients identified 5 different types. We found no clustering among the enzyme types by age, race/ethnicity, community area, or time.
Conclusions. Serogroup Y emerged as the most frequent cause of meningococcal disease in Chicago in 1995 and accounted for a substantial proportion of cases in 1996 and 1997. Current data suggest that the magnitude of serogroup Y meningococcal disease is sufficient for vaccine developers to incorporate serogroup Y into new vaccines.
From the Chicago Department of Public Health, Chicago, Ill (Drs Racoosin, Whitney, Conover, and Diaz); Centers for Disease Control and Prevention, Atlanta, Ga (Drs Whitney and Conover); and University of Illinois at Chicago, School of Public Health (Dr Racoosin).
RELATED ARTICLE
December 23/30, 1998
JAMA. 1998;280(24):2185-2186.
EXTRACT
| FULL TEXT
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES
 |
Genetic and Antigenic Analysis of Invasive Serogroup Y Neisseria meningitidis Isolates Collected from 1999 to 2003 in Canada
Tsang et al.
J. Clin. Microbiol. 2007;45:1753-1758.
ABSTRACT
| FULL TEXT
Pneumonia and Empyema Caused by Penicillin-Resistant Neisseria meningitidis: A Case Report and Literature Review
Glikman et al.
Pediatrics 2006;117:e1061-e1066.
ABSTRACT
| FULL TEXT
Prospects for Vaccine Prevention of Meningococcal Infection
Harrison
Clin. Microbiol. Rev. 2006;19:142-164.
ABSTRACT
| FULL TEXT
Genetic Basis for Biosynthesis of the ({alpha}1->4)-Linked N-Acetyl-D-Glucosamine 1-Phosphate Capsule of Neisseria meningitidis Serogroup X
Tzeng et al.
Infect. Immun. 2003;71:6712-6720.
ABSTRACT
| FULL TEXT
Fatal Acute Cellulitis Due to Neisseria meningitidis
Cartolano et al.
J. Clin. Microbiol. 2003;41:3996-3997.
ABSTRACT
| FULL TEXT
Meningococcal Disease
Rosenstein et al.
NEJM 2001;344:1378-1388.
FULL TEXT
Functional Opsonic Activity of Human Serum Antibodies to Inner Core Lipopolysaccharide (galE) of Serogroup B Meningococci Measured by Flow Cytometry
Plested et al.
Infect. Immun. 2001;69:3203-3213.
ABSTRACT
| FULL TEXT
Update on Meningococcal Disease with Emphasis on Pathogenesis and Clinical Management
van Deuren et al.
Clin. Microbiol. Rev. 2000;13:144-166.
ABSTRACT
| FULL TEXT
Epidemic Serogroup B Meningococcal Disease in Oregon: The Evolving Epidemiology of the ET-5 Strain
Diermayer et al.
JAMA 1999;281:1493-1497.
ABSTRACT
| FULL TEXT
Serogroup Y Meningococcal Disease on the Rise
JWatch Infect. Diseases 1999;1999:6-6.
FULL TEXT
|