Risk Factors for Invasive Pneumococcal Disease in Children in the Era of Conjugate Vaccine Use

Author:

Pilishvili Tamar1,Zell Elizabeth R.1,Farley Monica M.2,Schaffner William3,Lynfield Ruth4,Nyquist Ann-Christine5,Vazquez Marietta6,Bennett Nancy M.7,Reingold Arthur8,Thomas Ann9,Jackson Delois1,Schuchat Anne1,Whitney Cynthia G.1

Affiliation:

1. Division of Bacterial Diseases, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia;

2. Department of Medicine, Emory University, Veterans Affairs Medical Center, Atlanta, Georgia;

3. Department of Preventive Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee;

4. Minnesota Department of Health, St Paul, Minnesota;

5. Children's Hospital, Aurora, Colorado;

6. Department of Pediatrics, Yale University, New Haven, Connecticut;

7. Department of Medicine, University of Rochester, Rochester, New York;

8. School of Public Health, University of California, Berkeley, California; and

9. Department of Human Services, Office of Disease Prevention and Epidemiology, Portland, Oregon

Abstract

OBJECTIVE: We conducted a case-control study to evaluate risk factors for invasive pneumococcal disease (IPD) among children who were aged 3 to 59 months in the era of pneumococcal conjugate vaccine (PCV7). METHODS: IPD cases were identified through routine surveillance during 2001–2004. We matched a median of 3 control subjects to each case patient by age and zip code. We calculated odds ratios for potential risk factors for vaccine-type and non–vaccine-type IPD by using multivariable conditional logistic regression. RESULTS: We enrolled 782 case patients (45% vaccine-type IPD) and 2512 matched control subjects. Among children who received any PCV7, children were at increased risk for vaccine-type IPD when they had underlying illnesses, were male, or had no health care coverage. Vaccination with PCV7 did not influence the risk for non–vaccine-type IPD. Presence of underlying illnesses increased the risk for non–vaccine-type IPD, particularly among children who were not exposed to household smoking. Non–vaccine-type case patients were more likely than control subjects to attend group child care, be male, live in low-income households, or have asthma; case patients were less likely than control subjects to live in households with other children. CONCLUSIONS: Vaccination with PCV7 has reduced the risk for vaccine-type IPD that is associated with race and group child care attendance. Because these factors are still associated with non–vaccine-type IPD risk, additional reductions in disparities should be expected with new, higher valency conjugate vaccines.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology and Child Health

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