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Olarte et al

The Pediatric Infectious Disease Journal • 

Volume 33, Number 10, October 2014

| 

www.pidj.com

© 2014 Lippincott Williams &Wilkins

We did not identify an association with a particular pneumococ-

cal serotype and

S. pneumoniae

-only infections. Moreover, we did

not observe a higher rate of recurrence or complications in patients

with

S. pneumoniae

-only infections.

H. influenzae

(52%) was over-

all the most common organism co-isolated with

S. pneumoniae

.

The proportion of sinus cultures positive for

S. pneumonia

e and

H.

influenzae

remained unchanged in the post-PCV13 era. However,

we found an increase of

Prevotella

spp. (+11%;

P

= 0.02) after the

introduction of PCV13. The importance of anaerobes in chronic

sinusitis has been previously described

2,3,5

and their role in pediatric

sinusitis seems to be controversial.

4

A recent study from Nether-

lands

22

reported that vaccination with PCV7 resulted in a shift in

bacterial composition of the nasopharyngeal microbiota of vacci-

nated healthy children, with an increase in abundance of anaerobic

bacteria, especially

Prevotella

spp. The change in the isolation rate

of

Prevotella

spp. that we observed could be related to variations

in the nasopharyngeal microbiota as a result of the introduction of

PCVs or secondary to sampling techniques and improved isolation

of anaerobic organisms.

Some limitations of our study should be recognized. First,

we only studied children with chronic sinusitis, mainly because

pediatric patients with acute sinusitis do not usually undergo a

sinus tap or endoscopic sinus procedure unless their presentation is

complicated with an orbital abscess or an intracranial process that

requires surgical drainage. Therefore, we cannot extrapolate these

results to patients with acute sinusitis. Second, 3 patients had recur-

rence of pneumococcal sinusitis during the study period, but their

isolates were not available. Thus, it is possible that we missed some

cases of chronic sinusitis positive for

S. pneumoniae

, underestimat-

ing the prevalence of pneumococcal chronic sinusitis. Third, it is

possible that cultures positive for

S. pneumoniae

reflect inadvertent

contamination of sinus specimen with nasopharyngeal flora and not

a true pathogen.

In conclusion, our study provides evidence of important

epidemiologic changes of pneumococcal chronic sinusitis among

children after the introduction of PCV13. We reported a significant

decline of

S. pneumoniae

isolation rate in children with chronic

sinusitis at TCH. This decrease of pneumococcal chronic sinusitis

cases was driven by a substantial reduction of PCV13 serotypes,

predominantly serotype 19A.

S. pneumoniae

continues to represent

an important pathogen in chronic sinusitis especially in children <5

years of age; however, additional studies are needed to fully under-

stand the microbiology of chronic sinusitis in children, particularly

in the PCV13 era.

ACKNOWLEDGMENTS

The authors thank Wendy Hammerman and Andrea Forbes

for their assistance obtaining the pneumococcal isolates and

immunization records.

REFERENCES

1. Wald ER, Applegate KE, Bordley C, et al.; American Academy of

Pediatrics. Clinical practice guideline for the diagnosis and management of

acute bacterial sinusitis in children aged 1 to 18 years.

Pediatrics

. 2013;132:

e262–e280.

2. Brook I. Bacteriology of chronic sinusitis and acute exacerbation of chronic

sinusitis.

Arch Otolaryngol Head Neck Surg

. 2006;132:1099–1101.

3. Puglisi S, Privitera S, Maiolino L, et al. Bacteriological findings and anti-

microbial resistance in odontogenic and non-odontogenic chronic maxillary

sinusitis.

J Med Microbiol

. 2011;60(pt 9):1353–1359.

4. Tinkelman DG, Silk HJ. Clinical and bacteriologic features of chronic sinus-

itis in children.

Am J Dis Child

. 1989;143:938–941.

5. Brook I. Bacteriologic features of chronic sinusitis in children.

JAMA

.

1981;246:967–969.

6. Kaplan SL, Mason EO Jr, Wald ER, et al. Decrease of invasive pneumococ-

cal infections in children among 8 children’s hospitals in the United States

after the introduction of the 7-valent pneumococcal conjugate vaccine.

Pediatrics

. 2004;113(3 pt 1):443–449.

7. Pilishvili T, Lexau C, Farley MM, et al.; Active Bacterial Core Surveillance/

Emerging Infections Program Network. Sustained reductions in inva-

sive pneumococcal disease in the era of conjugate vaccine.

J Infect Dis

.

2010;201:32–41.

8. Casey JR, Pichichero ME. Changes in frequency and pathogens causing

acute otitis media in 1995-2003.

Pediatr Infect Dis J

. 2004;23:824–828.

9. Block SL, Hedrick J, Harrison CJ, et al. Community-wide vaccination with

the heptavalent pneumococcal conjugate significantly alters the microbiol-

ogy of acute otitis media.

Pediatr Infect Dis J

. 2004;23:829–833.

10. Brook I, Gober AE. Frequency of recovery of pathogens from the nasophar-

ynx of children with acute maxillary sinusitis before and after the introduc-

tion of vaccination with the 7-valent pneumococcal vaccine.

Int J Pediatr

Otorhinolaryngol

. 2007;71:575–579.

11. Brook I, Foote PA, Hausfeld JN. Frequency of recovery of pathogens caus-

ing acute maxillary sinusitis in adults before and after introduction of

vaccination of children with the 7-valent pneumococcal vaccine.

J Med

Microbiol

. 2006;55(pt 7):943–946.

12. McNeil JC, Hulten KG, Mason EO Jr, et al. Serotype 19A is the most com-

mon

Streptococcus pneumoniae

isolate in children with chronic sinusitis.

Pediatr Infect Dis J

. 2009;28:766–768.

13. Kaplan SL, Barson WJ, Lin PL, et al. Serotype 19A Is the most common

serotype causing invasive pneumococcal infections in children.

Pediatrics

.

2010;125:429–436.

14. Kaplan SL, Barson WJ, Lin PL, et al. Early trends for invasive pneumococ-

cal infections in children after the introduction of the 13-valent pneumococ-

cal conjugate vaccine.

Pediatr Infect Dis J

. 2013;32:203–207.

15. Clinical and Laboratory Standards Institute.

Performance Standards for

Antimicrobial Testing; Twenty-second Informational Supplement, CLSI docu-

ment M100-S22

. Wayne, PA: Clinical and Laboratory Standards Institute; 2012.

16. Merino LA, Ronconi MC, Hreñuk GE, et al. Bacteriologic findings in

patients with chronic sinusitis.

Ear Nose Throat J

. 2003;82:798–800, 803–

794, 806.

17. Center for Disease Control and Prevention. Update on effectiveness and

impact of PCV13 use among U.S. children. Available at:

www.cdc.gov/vac- cines/acip/meetings/downloads//slides-oct-2013/02-Pneumococcal-Moore. pdf

. Accessed April 1, 2014.

18. LoughlinAM, Hsu K, SilverioAL, et al. Direct and Indirect Effects of PCV13

on Nasopharyngeal Carriage of PCV13 Unique Pneumococcal Serotypes in

Massachusetts’ Children.

Pediatr Infect Dis J

. 2014;33:504–510.

19. Lee GM, Kleinman K, Pelton SI, et al. Impact of 13-valent pneumococcal

conjugate vaccination on

Streptococcus pneumoniae

carriage in young chil-

dren in Massachusetts.

J Pediatric Infect Dis Soc

. 2014;3:23–32.

20. Dagan R, Leibovitz E, Greenberg D, et al. Mixed pneumococcal-nontype-

able

Haemophilus influenzae

otitis media is a distinct clinical entity with

unique epidemiologic characteristics and pneumococcal serotype distribu-

tion.

J Infect Dis

. 2013;208:1152–1160.

21. Xu Q, Casey JR, Chang A, et al. When co-colonizing the nasopharynx

Haemophilus influenzae

predominates over

Streptococcus pneumoniae

except serotype 19A strains to cause acute otitis media.

Pediatr Infect Dis J

.

2012;31:638–640.

22. Biesbroek G, Wang X, Keijser BJ, et al. Seven-valent pneumococcal con-

jugate vaccine and nasopharyngeal microbiota in healthy children.

Emerg

Infect Dis

. 2014;20:201–210.

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