Impact of 13-Valent Pneumococcal Conjugate Vaccination on Streptococcus pneumoniae Carriage in Young Children in Massachusetts
Background In April 2010, a 13-valent pneumococcal conjugate vaccine (PCV13) replaced PCV7 for use in the United States. We evaluated rates of pneumococcal colonization, by serotype and antibiotic resistance, in Massachusetts communities where serial cross-sectional surveillance has been conducted f...
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Published in: | Journal of the Pediatric Infectious Diseases Society Vol. 3; no. 1; pp. 23 - 32 |
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England
Oxford University Press
01-03-2014
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Abstract | Background
In April 2010, a 13-valent pneumococcal conjugate vaccine (PCV13) replaced PCV7 for use in the United States. We evaluated rates of pneumococcal colonization, by serotype and antibiotic resistance, in Massachusetts communities where serial cross-sectional surveillance has been conducted for the past decade.
Methods
Nasopharyngeal swabs were obtained from children 0 to <7 years of age and seen by primary care providers for well child or acute illness visits in 2001, 2004, 2007, 2009, and 2011. Pneumococcal isolates were serotyped by Quellung reaction and classified as PCV7 serotypes (4, 6B, 9V, 14, 18C, 19F, 23F), additional PCV13 serotypes (1, 3, 5, 6A, 7F, 19A), or non-PCV13 serotypes. Changes in colonization and impact of PCV13 were assessed using generalized linear mixed models, adjusting for known risk factors and accounting for clustering by community.
Results
Introduction of PCV13 did not affect the rate of overall pneumococcal colonization (31% in 2011). Colonization with non-PCV13 serotypes increased between 2001 and 2011 for all children (odds ratio [OR] per year, 1.12; 95% confidence interval [CI], 1.10, 1.15; P < .0001). 19A remained the second most common serotype in 2011, although a decline from 2009 was observed. Penicillin (7%), erythromycin (28%), ceftriaxone (10%), and clindamycin (10%) nonsusceptibility were commonly identified, concentrated among a small number of serotypes (including 19A, 35B, 15B/C, and 15A). Among healthy children 6–23 months old, colonization with PCV13 serotypes was lower among recipients of PCV13 vaccine (adjusted OR, 0.30; 95% CI, 0.11, 0.78). This effect was not observed in 6- to 23-month-old children with a concomitant respiratory tract infection (adjusted OR 1.36; 95% CI, 0.66, 2.77) or children 2 to <7 years old (adjusted OR, 1.17; 95% CI, 0.58, 2.34).
Conclusions
13-Valent pneumococcal conjugate vaccine reduced the prevalence of colonization with PCV13 serotypes among children 6–23 months old, but its efficacy was not shown among older children. |
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AbstractList | In April 2010, a 13-valent pneumococcal conjugate vaccine (PCV13) replaced PCV7 for use in the United States. We evaluated rates of pneumococcal colonization, by serotype and antibiotic resistance, in Massachusetts communities where serial cross-sectional surveillance has been conducted for the past decade.
Nasopharyngeal swabs were obtained from children 0 to <7 years of age and seen by primary care providers for well child or acute illness visits in 2001, 2004, 2007, 2009, and 2011. Pneumococcal isolates were serotyped by Quellung reaction and classified as PCV7 serotypes (4, 6B, 9V, 14, 18C, 19F, 23F), additional PCV13 serotypes (1, 3, 5, 6A, 7F, 19A), or non-PCV13 serotypes. Changes in colonization and impact of PCV13 were assessed using generalized linear mixed models, adjusting for known risk factors and accounting for clustering by community.
Introduction of PCV13 did not affect the rate of overall pneumococcal colonization (31% in 2011). Colonization with non-PCV13 serotypes increased between 2001 and 2011 for all children (odds ratio [OR] per year, 1.12; 95% confidence interval [CI], 1.10, 1.15; P < .0001). 19A remained the second most common serotype in 2011, although a decline from 2009 was observed. Penicillin (7%), erythromycin (28%), ceftriaxone (10%), and clindamycin (10%) nonsusceptibility were commonly identified, concentrated among a small number of serotypes (including 19A, 35B, 15B/C, and 15A). Among healthy children 6-23 months old, colonization with PCV13 serotypes was lower among recipients of PCV13 vaccine (adjusted OR, 0.30; 95% CI, 0.11, 0.78). This effect was not observed in 6- to 23-month-old children with a concomitant respiratory tract infection (adjusted OR 1.36; 95% CI, 0.66, 2.77) or children 2 to <7 years old (adjusted OR, 1.17; 95% CI, 0.58, 2.34).
13-Valent pneumococcal conjugate vaccine reduced the prevalence of colonization with PCV13 serotypes among children 6-23 months old, but its efficacy was not shown among older children. Background In April 2010, a 13-valent pneumococcal conjugate vaccine (PCV13) replaced PCV7 for use in the United States. We evaluated rates of pneumococcal colonization, by serotype and antibiotic resistance, in Massachusetts communities where serial cross-sectional surveillance has been conducted for the past decade. Methods Nasopharyngeal swabs were obtained from children 0 to <7 years of age and seen by primary care providers for well child or acute illness visits in 2001, 2004, 2007, 2009, and 2011. Pneumococcal isolates were serotyped by Quellung reaction and classified as PCV7 serotypes (4, 6B, 9V, 14, 18C, 19F, 23F), additional PCV13 serotypes (1, 3, 5, 6A, 7F, 19A), or non-PCV13 serotypes. Changes in colonization and impact of PCV13 were assessed using generalized linear mixed models, adjusting for known risk factors and accounting for clustering by community. Results Introduction of PCV13 did not affect the rate of overall pneumococcal colonization (31% in 2011). Colonization with non-PCV13 serotypes increased between 2001 and 2011 for all children (odds ratio [OR] per year, 1.12; 95% confidence interval [CI], 1.10, 1.15; P < .0001). 19A remained the second most common serotype in 2011, although a decline from 2009 was observed. Penicillin (7%), erythromycin (28%), ceftriaxone (10%), and clindamycin (10%) nonsusceptibility were commonly identified, concentrated among a small number of serotypes (including 19A, 35B, 15B/C, and 15A). Among healthy children 6–23 months old, colonization with PCV13 serotypes was lower among recipients of PCV13 vaccine (adjusted OR, 0.30; 95% CI, 0.11, 0.78). This effect was not observed in 6- to 23-month-old children with a concomitant respiratory tract infection (adjusted OR 1.36; 95% CI, 0.66, 2.77) or children 2 to <7 years old (adjusted OR, 1.17; 95% CI, 0.58, 2.34). Conclusions 13-Valent pneumococcal conjugate vaccine reduced the prevalence of colonization with PCV13 serotypes among children 6–23 months old, but its efficacy was not shown among older children. BACKGROUNDIn April 2010, a 13-valent pneumococcal conjugate vaccine (PCV13) replaced PCV7 for use in the United States. We evaluated rates of pneumococcal colonization, by serotype and antibiotic resistance, in Massachusetts communities where serial cross-sectional surveillance has been conducted for the past decade. METHODSNasopharyngeal swabs were obtained from children 0 to <7 years of age and seen by primary care providers for well child or acute illness visits in 2001, 2004, 2007, 2009, and 2011. Pneumococcal isolates were serotyped by Quellung reaction and classified as PCV7 serotypes (4, 6B, 9V, 14, 18C, 19F, 23F), additional PCV13 serotypes (1, 3, 5, 6A, 7F, 19A), or non-PCV13 serotypes. Changes in colonization and impact of PCV13 were assessed using generalized linear mixed models, adjusting for known risk factors and accounting for clustering by community. RESULTSIntroduction of PCV13 did not affect the rate of overall pneumococcal colonization (31% in 2011). Colonization with non-PCV13 serotypes increased between 2001 and 2011 for all children (odds ratio [OR] per year, 1.12; 95% confidence interval [CI], 1.10, 1.15; P < .0001). 19A remained the second most common serotype in 2011, although a decline from 2009 was observed. Penicillin (7%), erythromycin (28%), ceftriaxone (10%), and clindamycin (10%) nonsusceptibility were commonly identified, concentrated among a small number of serotypes (including 19A, 35B, 15B/C, and 15A). Among healthy children 6-23 months old, colonization with PCV13 serotypes was lower among recipients of PCV13 vaccine (adjusted OR, 0.30; 95% CI, 0.11, 0.78). This effect was not observed in 6- to 23-month-old children with a concomitant respiratory tract infection (adjusted OR 1.36; 95% CI, 0.66, 2.77) or children 2 to <7 years old (adjusted OR, 1.17; 95% CI, 0.58, 2.34). CONCLUSIONS13-Valent pneumococcal conjugate vaccine reduced the prevalence of colonization with PCV13 serotypes among children 6-23 months old, but its efficacy was not shown among older children. |
Author | Stevenson, Abbie Pelton, Stephen I. Hanage, William Finkelstein, Jonathan A. Lakoma, Matthew Dutta-Linn, Maya Croucher, Nicholas J. Lee, Grace M. Kleinman, Ken Huang, Susan S. |
AuthorAffiliation | 1 Center for Child Health Care Studies, Department of Population Medicine, Harvard Pilgrim Health Care Institute and Harvard Medical School 5 Division of Infectious Diseases, University of California Irvine 3 Department of Pediatrics, Boston University School of Medicine 4 Department of Epidemiology, Harvard School of Public Health, Boston, Massachusetts 6 Department of Medicine, Boston Children's Hospital, Massachusetts 2 Division of Infectious Diseases and Department of Laboratory Medicine, Boston Children's Hospital |
AuthorAffiliation_xml | – name: 5 Division of Infectious Diseases, University of California Irvine – name: 3 Department of Pediatrics, Boston University School of Medicine – name: 2 Division of Infectious Diseases and Department of Laboratory Medicine, Boston Children's Hospital – name: 1 Center for Child Health Care Studies, Department of Population Medicine, Harvard Pilgrim Health Care Institute and Harvard Medical School – name: 6 Department of Medicine, Boston Children's Hospital, Massachusetts – name: 4 Department of Epidemiology, Harvard School of Public Health, Boston, Massachusetts |
Author_xml | – sequence: 1 givenname: Grace M. surname: Lee fullname: Lee, Grace M. email: grace.lee@childrens.harvard.edu organization: 1 Center for Child Health Care Studies, Department of Population Medicine, Harvard Pilgrim Health Care Institute and Harvard Medical School – sequence: 2 givenname: Ken surname: Kleinman fullname: Kleinman, Ken organization: 1 Center for Child Health Care Studies, Department of Population Medicine, Harvard Pilgrim Health Care Institute and Harvard Medical School – sequence: 3 givenname: Stephen I. surname: Pelton fullname: Pelton, Stephen I. organization: 3 Department of Pediatrics, Boston University School of Medicine – sequence: 4 givenname: William surname: Hanage fullname: Hanage, William organization: 4 Department of Epidemiology, Harvard School of Public Health, Boston, Massachusetts – sequence: 5 givenname: Susan S. surname: Huang fullname: Huang, Susan S. organization: 5 Division of Infectious Diseases, University of California Irvine – sequence: 6 givenname: Matthew surname: Lakoma fullname: Lakoma, Matthew organization: 1 Center for Child Health Care Studies, Department of Population Medicine, Harvard Pilgrim Health Care Institute and Harvard Medical School – sequence: 7 givenname: Maya surname: Dutta-Linn fullname: Dutta-Linn, Maya organization: 1 Center for Child Health Care Studies, Department of Population Medicine, Harvard Pilgrim Health Care Institute and Harvard Medical School – sequence: 8 givenname: Nicholas J. surname: Croucher fullname: Croucher, Nicholas J. organization: 4 Department of Epidemiology, Harvard School of Public Health, Boston, Massachusetts – sequence: 9 givenname: Abbie surname: Stevenson fullname: Stevenson, Abbie organization: 4 Department of Epidemiology, Harvard School of Public Health, Boston, Massachusetts – sequence: 10 givenname: Jonathan A. surname: Finkelstein fullname: Finkelstein, Jonathan A. organization: 1 Center for Child Health Care Studies, Department of Population Medicine, Harvard Pilgrim Health Care Institute and Harvard Medical School |
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Keywords | colonization pneumococcal conjugate vaccine Streptococcus pneumoniae |
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References_xml | – volume: 59 start-page: 253 issn: 0149-2195 issue: 9 year: 2010 ident: 1_36799940 publication-title: MMWR. Morbidity and mortality weekly report – volume: 193 start-page: 1487 issn: 0022-1899 issue: 11 year: 2006 ident: 24_38436257 publication-title: Journal of Infectious Diseases doi: 10.1086/503805 – volume: 112 start-page: 862 issn: 0031-4005 issue: 4 year: 2003 ident: 16_17840169 publication-title: Pediatrics doi: 10.1542/peds.112.4.862 contributor: fullname: Finkelstein – volume: 203 start-page: 1360 issn: 0022-1899 issue: 10 year: 2011 ident: 31_39410643 publication-title: Journal of Infectious Diseases doi: 10.1093/infdis/jir052 – volume: 29 start-page: 7207 issn: 0264-410X year: 2011 ident: 29_46256298 publication-title: Vaccine doi: 10.1016/j.vaccine.2011.06.056 – volume: 14411 start-page: 3049 issn: 1350-0872 year: 1998 ident: 18_46613957 publication-title: Microbiology – volume: 11 start-page: 760 issn: 1473-3099 issue: 10 year: 2011 ident: 26_40031295 publication-title: The Lancet infectious diseases doi: 10.1016/S1473-3099(11)70090-1 contributor: fullname: Miller – volume: 60 start-page: 1477 issn: 0149-2195 issue: 43 year: 2011 ident: 23_41154679 publication-title: MMWR. Morbidity and mortality weekly report – volume: 31 start-page: 249 issn: 0891-3668 issue: 3 year: 2012 ident: 10_41801767 publication-title: The Pediatric infectious disease journal doi: 10.1097/INF.0b013e31824214ac – volume: 126 start-page: 186 issn: 0031-4005 issue: 1 year: 2010 ident: 12_37323300 publication-title: Pediatrics doi: 10.1542/peds.2010-1280 – volume: 204 start-page: 1857 issn: 0022-1899 issue: 12 year: 2011 ident: 27_40785567 publication-title: Journal of Infectious Diseases doi: 10.1093/infdis/jir618 – volume: 137 start-page: 555 issn: 1469-4409 issue: 4 year: 2009 ident: 22_31633952 publication-title: Epidemiology and Infection (Print) doi: 10.1017/S0950268808001143 contributor: fullname: Pebody – volume: 196 start-page: 1211 issn: 0022-1899 issue: 8 year: 2007 ident: 2_38590108 publication-title: Journal of Infectious Diseases doi: 10.1086/521833 – volume: 31 start-page: 297 issn: 0891-3668 issue: 3 year: 2012 ident: 32_41966504 publication-title: The Pediatric infectious disease journal doi: 10.1097/INF.0b013e318247ef84 contributor: fullname: Cohen – volume: 50 start-page: 1238 issn: 1058-4838 issue: 9 year: 2010 ident: 5_38637474 publication-title: Clinical Infectious Diseases doi: 10.1086/651680 – volume: 187 start-page: 6223 issn: 0021-9193 issue: 17 year: 2005 ident: 17_19337895 publication-title: Journal of Bacteriology doi: 10.1128/JB.187.17.6223-6230.2005 contributor: fullname: Hanage – volume: 132 start-page: 62 issn: 0022-1899 issue: 1 year: 1975 ident: 28_38724504 publication-title: Journal of Infectious Diseases doi: 10.1093/infdis/132.1.62 – volume: 28 start-page: 7634 issn: 0264-410X year: 2010 ident: 13_46189496 publication-title: Vaccine doi: 10.1016/j.vaccine.2010.09.049 – volume: 54 start-page: 893 issn: 0149-2195 issue: 36 year: 2005 ident: 25_19407260 publication-title: MMWR. Morbidity and mortality weekly report – volume: 26 start-page: 468 issn: 0891-3668 issue: 6 year: 2007 ident: 14_28781434 publication-title: The Pediatric infectious disease journal doi: 10.1097/INF.0b013e31803df9ca – volume: 68 start-page: 439 issn: 0732-8893 issue: 4 year: 2010 ident: 30_38694311 publication-title: Diagnostic microbiology and infectious disease doi: 10.1016/j.diagmicrobio.2010.07.020 contributor: fullname: Ho – volume: 26 start-page: 468 issn: 0891-3668 issue: 6 year: 2007 ident: 3_28781434 publication-title: The Pediatric infectious disease journal doi: 10.1097/INF.0b013e31803df9ca contributor: fullname: Pelton – volume: 29 start-page: 8877 issn: 0264-410X year: 2011 ident: 15_46613956 publication-title: Vaccine doi: 10.1016/j.vaccine.2011.09.075 – volume: 31 start-page: 249 issn: 0891-3668 issue: 3 year: 2012 ident: 6_41801767 publication-title: The Pediatric infectious disease journal doi: 10.1097/INF.0b013e31824214ac contributor: fullname: Wroe |
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In April 2010, a 13-valent pneumococcal conjugate vaccine (PCV13) replaced PCV7 for use in the United States. We evaluated rates of pneumococcal... In April 2010, a 13-valent pneumococcal conjugate vaccine (PCV13) replaced PCV7 for use in the United States. We evaluated rates of pneumococcal colonization,... BACKGROUNDIn April 2010, a 13-valent pneumococcal conjugate vaccine (PCV13) replaced PCV7 for use in the United States. We evaluated rates of pneumococcal... |
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Title | Impact of 13-Valent Pneumococcal Conjugate Vaccination on Streptococcus pneumoniae Carriage in Young Children in Massachusetts |
URI | https://www.ncbi.nlm.nih.gov/pubmed/24567842 https://search.proquest.com/docview/1738818916 https://pubmed.ncbi.nlm.nih.gov/PMC3933044 |
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