1470. Epidemiology of Invasive Pneumococcal Disease (IPD) Following 18 years of Pneumococcal Conjugate Vaccine (PCV) Use in the United States

Author:

Pilishvili Tamara1,Gierke Ryan2,Farley Monica M3,Schaffner William4,Thomas Ann5,Reingold Art6,Harrison Lee7,Holtzman Corinne8,Burzlaff Kari9,Petit Susan10,Herlihy Rachel11,Torres Salina12,Beall Bernard2

Affiliation:

1. Centers for Disease Control and Prevention, Atlanta, GA, USA, Atlanta, Georgia

2. Centers for Disease Control and Prevention, Atlanta, Georgia

3. Emory University, Atlanta, Georgia

4. Vanderbilt University Medical Center, Nashville, Tennessee

5. Oregon Public Health Division, Portland, Oregon

6. University of California, Berkeley, Berkeley, CA

7. University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania

8. Minnesota Department of Health, St. Paul, Minnesota

9. New York State Department of Health, Buffalo, New York

10. Connecticut Department of Public Health, Hartford, Connecticut

11. Colorado Department of Public Health and Environment, Denver, Colorado

12. New Mexico Department of Health, Santa Fe, New Mexico

Abstract

Abstract Background PCVs have been recommended for U.S. children since 2000. A 7-valent vaccine (PCV7) was introduced in 2000. This was replaced by a 13-valent vaccine (PCV13) in 2010. PCV13 was also recommended for adults aged ≥ 65 years in August 2014. We evaluated PCV impact on IPD. Methods IPD cases (isolation of pneumococcus from sterile sites) were identified through CDC’s Active Bacterial Core surveillance during 1998-2018. Isolates were serotyped by Quellung or whole genome sequencing and classified as PCV13-type and non-vaccine-type (NVT). Incidence rates (cases/100,000) were calculated using U.S. Census Bureau population denominators. Results From 1998 through 2018, overall IPD rates among children aged < 5 years decreased by 93% (from 95 to 7 cases/100,000). PCV13-type IPD decreased by 98% (from 88 to 2 cases/100,000). Among adults aged ≥ 65 years, overall IPD rates decreased by 60% (from 61 to 25 cases/100,000). PCV13-type IPD rates declined 86% (from 46 to 7 cases/100,000). Declines were most dramatic in the years following PCV7 introduction, with additional declines after PCV13 introduction in children (Figures 1 and 2). Serotypes 3, 19A, and 19F caused most of the remaining PCV13-type IPD. NVT IPD rates did not change significantly among children. Among adults aged 50-64 years, NVT IPD increased by 83% (from 6 to 12 cases/100,000) (p< 0.01). Among adults aged ≥ 65 years, NVT IPD increased by 22% (from 15 to 18 cases/100,000) (p< 0.01). The most common NVTs in 2018 were 22F (10% of all IPD), 9N (7%) and 15A (5%). Among children, the proportion of cases with meningitis increased from 5% to 14% (p< 0.01), and the proportion with pneumonia/empyema increased from 17% to 31% (p< 0.01). Among adults, the proportion of cases with meningitis did not change (3%), while the proportion with pneumonia/empyema increased from 72% to 76% (p=0.01). Figure 1: Incidence of invasive pneumococcal disease among children aged < 5 years, 1998-2018 Figure 2: Incidence of invasive pneumococcal disease among adults aged ≥ 65 years, 1998-2018 Conclusion Overall IPD incidence among children and adults decreased following PCV introduction for children, driven primarily by reductions in PCV-type IPD. NVT IPD increased in older adults, but these increases did not eliminate reductions from PCV13-type IPD. Disclosures Lee Harrison, MD, GSK (Consultant)Merck (Consultant)Pfizer (Consultant)Sanofi Pasteur (Consultant)

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

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