Pneumococcal 02 Gierke 508

CDC ACIP — Vaccine Advisory Committee

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National Center for Immunization & Respiratory Diseases       
     
  
    
    Current Epidemiology of Pediatric Pneumococcal 
Disease, United States 
Ryan Gierke, MPH 
Advisory Committee on Immunization Practices 
Feb 22, 2023 
1 
     
        
 
 Pneumococcal carriage is precursor to pneumococcal disease 
Noninvasive Disease 
Invasive Disease More frequent 
Less frequent 
Bogaert, Lancet Infect Dis 2004;4:144-54 2 
    
        
  
        
       
    
  
  
  
      
  Outline 
 Invasive Pneumococcal Disease (IPD) in children 
• Impact of Pneumococcal Conjugate Vaccines (PCVs) on IPD incidence and 
serotype distribution 
• IPD incidence caused by serotypes in PCV15 and PCV20 
• Changes in IPD incidence and serotype distribution post-COVID19 
 Acute Otitis Media (AOM) 
• Impact of PCV13 
• Incidence Estimates 
 Pneumonia in children • Impact of PCV13 on all-cause and pneumococcal pneumonia 
• Incidence Estimates 
3 

       
      
   Impact of PCVs on Invasive Pneumococcal Disease 
(IPD) Incidence and Serotype Distribution among 
Children in the U.S. 
4 
     
    
  
  
           
       
         
         Methods 
 Active Bacterial Core surveillance (ABCs): 
 Active laboratory and population-based 
surveillance, 10 sites 
 Pneumococcus isolation from sterile site 
 Isolates serotyped by whole genome sequencing, Quellung, or PCR at reference labs and grouped for analysis by vaccine type 
 US Census Bureau race-bridged post-census population estimates used as denominators 
 Overall and serotype-specific IPD incidence rates (cases per 100,000 people) 
5 
               
  
  
  
 Incidence rates of invasive pneumococcal disease (IPD) among children < 5 
years old, 1998–2019 
0 10 20 30 40 50 60 70 80 90 100 Cases per 100,000 persons All IPD PCV13+6C Non-PCV13 PCV7 introduction 
PCV13 introduction 
children * 
1998 1999 2000 2001 2002 2003 2004 2005 2006 2007 2008 2009 2010 2011 2012 2013 2014 2015 2016 2017 2018 2019 
Year 
                *Serotype 6C was grouped with PCV13 serotypes due to cross protection from 6A antigen in the vaccine 6 
   
             
   
 Incidence rates of invasive pneumococcal disease (IPD) among children < 5 
years old, 2007 – 2021 
25 
20 15 
10 
5 
0 
2007 2008 2009 2010 2011 2012 2013 2014 
Year 2015 2016 2017 2018 2019 2020 2021 Cases per 100,000 ALL IPD 
PCV13 + 6C 
Non-PCV13 PCV13: children 
COVID-19 * 
                7 
*Serotype 6C was grouped with PCV13 serotypes due to cross protection from 6A antigen in the vaccine 
Incidence rates of IPD among children < 5 years old, 2011 – 2021, 
by PCV13+6C*serotypes 
2011 2012 2013 2014 2015 2016 2017 2018 2019 2020 2021 
Year 0.0 0.5 1.0 1.5 2.0 2.5 3.0 3.5 4.0 4.5 5.0 Cases per 100,000 population 001 005 
PCV7 (except 19F) 19F 
06C 003 
07F 19A % of PCV13+6C serotypes 
2018-2019 2020-2021 
003 46% 18% 
19F 32% 60% 
19A 14% 18% 
06C 4% 0% 
COVID-19                     
   
                *Serotype 6C was grouped with PCV13 serotypes due to cross protection from 6A antigen in the vaccine 8 
       
    Current Pediatric Pneumococcal Disease Incidence Caused by 
Serotypes in PCV15 and PCV20 
9 
       
  
         
    
      
         
        Serotypes contained in current and new pneumococcal 
vaccines 
1 3 4 5 6A 6B 7 F 9V 14 18 
C 19 
A 19 F 23 F 22 F 33 F 8 10 A 11 A 12 F 15 B 2 9N 17 
F 20 
PCV13 
PCV15 PCV20 PPSV23 
For analysis purposes: 
• PCV13+6C : includes serotype 6C with PCV13 types due to cross 
protection from 6A antigen 
• PCV15 non-PCV13 : includes serotypes 22F and 33F 
• PCV20 non-PCV15 : includes serotypes 8, 10A, 11A, 12F, and 15B 
• PPSV23 non-PCV20 : includes serotypes 2, 9N, 17F, and 20 
10 
Incidence rates of IPD among children <5 years old, 
2011 – 2021, by vaccine type 
14 
12 10 
8 6 4 2 
0 
2011 2012 2013 2014 2015 2016 2017 2018 2019 2020 2021 PCV13+6C PCV15/ non-PCV13 PCV20/ non-PCV15 
PPSV23/ non-PCV20 Non-Vaccine Type 
COVID-19 Proportion of IPD 
2018-2019 2020-2021 
Non-Vaccine Type 46% 52% 
PPSV23/ non-PCV20 1% 4% 
PCV20/ non-PCV15 15% 13% 
PCV15/ non-PCV13 17% 15% 
PCV13+6C 21% 16%        
         
    
 
 
 
 
Year Cases per 100,000 population 
    
       
       PCV15 non-PCV13 serotypes: 22F, 33F P
CV20 non-PCV15 serotypes: 8, 10A, 11A, 12F, 15B 
PPSV23 non-PCV20 serotype: 2, 9N, 17F ,20 11 
     
    
 
 
 
           
    Incidence rates of IPD among children 5 -18 years old, 
2011 – 2021, by vaccine type Cases per 100,000 population 
0.0 0.5 1.0 1.5 2.0 2.5 
2011 2012 2013 2014 2015 2016 2017 2018 2019 2020 2021 PCV13+6C PCV15/ non-PCV13 PCV20/ non-PCV15 
PPSV23/ non-PCV20 Non-Vaccine Type % of IPD 
2018-2019 2020-2021 
Non-Vaccine Type 32% 36% 
PPSV23/ non-PCV20 5% 5% 
PCV20/ non-PCV15 13% 16% 
PCV15/ non-PCV13 16% 9% 
PCV13+6C 34% 34% 
COVID-19 
    
       
       Year 
PCV15 non-PCV13 serotypes: 22F, 33F PCV20 non-PCV15 serotypes: 8, 10A, 11A, 12F, 15B PPSV23 non-PCV20 serotype: 2, 9N, 17F ,20 12 
                       
 
                         
 
      
  
     
 
 
 IPD incidence among children with 
immunocompromising conditions, 2015-2019* 
Children < 5 years Children 5-17 years 
10000 10000 Rate Ratio=231 
Rate Ratio=29 
1 Cases Per 100,000 persons 
(Log scale) 1000 
Cases Per 100,000 persons 
(Log scale) 1000 
Rate Ratio=71 
100 100 
10 
Sickle Cell Diseaseˆ 10 
1 
Hematologic Malignancy Sickle Cell Diseaseˆ 
Condition No condition Condition No condition 
                  
               CDC 
unpublished data, IPD cases identified from ABCs 
*Hematologic Malignancy Data only available from 2015-2018 for children age <5 years 
ˆ IPD rates for those with and without sickle cell disease are among African American children 13 
Acute  Otitis  Media  (AOM) i n Children 
14 
       
       
      
      
     
        
    
    
     
   PCV13 impact on acute otitis media in children 
 AOM is a major cause of childhood morbidity1,2,3 
• Pneuococcus is a common bacterial cause of AOM 
• S. pneumoniae accounted for an estimated 24%4 
 AOM incidence decreased after PCV13 introduction 
• 11%-14% decrease, depending on age group and study years1,2 
1 Tong et al. BMC 2018 
2 King et al. ASHE 2021 
3Casey et al Clin Pediatr 2014; 
4Kaur et al. EJCMID 2022 15 

     
 
 
 
       
   
    Incidence of acute otitis media among children 
AOM visits per 100,000 Person Years 
20141 2014-20182 2016-20183 
<1 43,180 -- --
1 year 47,860 -- --
<2 years -- 76,880 49,050 
2-4 years 29,980 41,030 31,970 
5-17 years 9,060 9,180 5,680 
AOM incidence highest 
among children age <5 years 
1  Ton  g et  al.  BMC 2018 
2  Hu  et  al.  BMC 2022 
3Unpublishe  d analysi  s courtesy  o f Laura  King,  U C Berkeley 16 

  Pneumonia in Children 
17 
       
          
   
    
           
         
   
   
   Evidence of PCV13 impact on pneumonia in children 
 Reduction in incidence of all-cause and pneumococcal pneumonia among in 
children following PCV13 introduction1,2,3 
• 17-35% reduction in all cause-pneumonia1 
• 40% and 51% reduction in inpatient pneumococcal pneumonia among ages <1 
and 5-17 years, respectively; no reductions in ages 2-4 years2 
1Tong et al. BMC 2018 
2 Simonsen et al. Lancet 2014 
18 3King et al. ASHE 2021 

  
     
        
       
    
 Pneumonia incidence among children 
Age (years) All-cause pneumonia (frequency per 
100,000 person years)1 , 2014 All-cause inpatient pneumonia (cases 
per 100,000 population)2 , 2018–19 
< 1 2,250 680 
1 3,990 480 
2–4 3,390 290 
5–17 1,280 87 
1 Tong et al. BMC 2018 
2 National Inpatient Sample, 2018-2019 
18 

           
   
          
   
          
    
    Conclusions 
• Use of PCVs (PCV7, PCV13) significantly decreased the incidence of pneumococcal 
disease in U.S. children 
• Risk of disease remains higher in children with immunocompromising conditions compared to children without 
• In 2018–2019, the proportion of IPD caused by vaccine serotypes was: 
• PCV20, non-PCV13: ~30% of IPD 
• PCV15, non-PCV13: ~15% of IPD 
20 

    
 
      
                  
         Questions 
For more information, contact CDC 
1-800-CDC-INFO (232-4636) TTY: 1-888-232-6348 www.cdc.gov 
The findings and conclusions in this report are those of the authors and do not necessarily represent the official position of the Centers for Disease Control and Prevention.