Streptococcus pneumoniae serotype 3 is masking PCV13-mediated herd immunity in Canadian adults hospitalized with community acquired pneumonia: A study from the Serious Outcomes Surveillance (SOS) Network of the Canadian immunization research Network (CIRN)

•The proportion of CAP attributed to S. pneumoniae declined from 2010 to 2014, but increased in 2015.•PCV13 serotypes in bacteremic and non-bacteremic pneumococcal CAP mirrored trends seen for S. pneumoniae positivity.•Herd immunity afforded by serotypes 7F and 19A was partly masked by a concomitant...

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Veröffentlicht in:Vaccine 2019-08, Vol.37 (36), p.5466-5473
Hauptverfasser: LeBlanc, Jason J., ElSherif, May, Ye, Lingyun, MacKinnon-Cameron, Donna, Ambrose, Ardith, Hatchette, Todd F., Lang, Amanda L.S., Gillis, Hayley D., Martin, Irene, Demczuk, Walter, Andrew, Melissa K., Boivin, Guy, Bowie, William, Green, Karen, Johnstone, Jennie, Loeb, Mark, McCarthy, Anne E., McGeer, Allison, Semret, Makeda, Trottier, Sylvie, Valiquette, Louis, Webster, Duncan, McNeil, Shelly A.
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container_end_page 5473
container_issue 36
container_start_page 5466
container_title Vaccine
container_volume 37
creator LeBlanc, Jason J.
ElSherif, May
Ye, Lingyun
MacKinnon-Cameron, Donna
Ambrose, Ardith
Hatchette, Todd F.
Lang, Amanda L.S.
Gillis, Hayley D.
Martin, Irene
Demczuk, Walter
Andrew, Melissa K.
Boivin, Guy
Bowie, William
Green, Karen
Johnstone, Jennie
Loeb, Mark
McCarthy, Anne E.
McGeer, Allison
Semret, Makeda
Trottier, Sylvie
Valiquette, Louis
Webster, Duncan
McNeil, Shelly A.
description •The proportion of CAP attributed to S. pneumoniae declined from 2010 to 2014, but increased in 2015.•PCV13 serotypes in bacteremic and non-bacteremic pneumococcal CAP mirrored trends seen for S. pneumoniae positivity.•Herd immunity afforded by serotypes 7F and 19A was partly masked by a concomitant increase in the proportion of serotype 3.•The shift in serotype distribution over time was not accompanied by changes in patient demographics or serious outcomes.•Despite herd immunity, pneumococcal CAP and IPD remain substantial cause of morbidity and mortality in hospitalized adults. The 13-valent pneumococcal conjugate vaccine (PCV13) was recently shown to be effective against PCV13-type invasive pneumococcal disease (IPD) and pneumococcal community acquired pneumonia (CAPSpn) in healthy adults aged ≥65 years, prompting many countries to re-assess adult immunization. In Canada, the potential benefits of adult PCV13 immunization were unclear given anticipated herd immunity from PCV13 childhood immunization introduced since 2010. This study describes the serotype distribution and clinical outcomes of Canadian adults aged ≥16 years, who were hospitalized with CAPSpn and IPD from 2010 to 2015. Active surveillance for CAP and IPD was performed in adult hospitals across five Canadian provinces. IPD was identified when Streptococcus pneumoniae was isolated from sterile sites. Bacteremic and non-bacteremic CAPSpn were identified using blood culture, and sputum culture or PCV13-specific urine antigen detection (UADPCV13), respectively. Serotype was assigned using Quellung reaction, PCR, or UADPCV13. Of 6687 CAP cases where a test was performed, S. pneumoniae positivity decreased from 15.9% in 2011 to 8.8% in 2014, but increased to 12.9% in 2015. CAPSpn attributed to PCV13 serotypes followed a similar trend, dropping from 8.3% in 2010 to 4.6% in 2014, but increasing to 6.3% in 2015. The decline was primarily attributed to serotypes 7F and 19A, and the proportional increase to serotype 3. Similar trends were noted for bacteremic and non-bacteremic CAPSpn. Serious outcomes such as 30-day mortality, intensive care unit admission, and requirement for mechanical ventilation were prominent in CAPSpn and IPD cases, but remained unchanged over the study years. Herd immunity afforded primarily by serotypes 7F and 19A appears to be partly masked by a concomitant proportional increase of serotype 3. Despite evidence of herd immunity, these PCV13 serotypes remain persistent in Ca
doi_str_mv 10.1016/j.vaccine.2019.05.003
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The 13-valent pneumococcal conjugate vaccine (PCV13) was recently shown to be effective against PCV13-type invasive pneumococcal disease (IPD) and pneumococcal community acquired pneumonia (CAPSpn) in healthy adults aged ≥65 years, prompting many countries to re-assess adult immunization. In Canada, the potential benefits of adult PCV13 immunization were unclear given anticipated herd immunity from PCV13 childhood immunization introduced since 2010. This study describes the serotype distribution and clinical outcomes of Canadian adults aged ≥16 years, who were hospitalized with CAPSpn and IPD from 2010 to 2015. Active surveillance for CAP and IPD was performed in adult hospitals across five Canadian provinces. IPD was identified when Streptococcus pneumoniae was isolated from sterile sites. Bacteremic and non-bacteremic CAPSpn were identified using blood culture, and sputum culture or PCV13-specific urine antigen detection (UADPCV13), respectively. Serotype was assigned using Quellung reaction, PCR, or UADPCV13. Of 6687 CAP cases where a test was performed, S. pneumoniae positivity decreased from 15.9% in 2011 to 8.8% in 2014, but increased to 12.9% in 2015. CAPSpn attributed to PCV13 serotypes followed a similar trend, dropping from 8.3% in 2010 to 4.6% in 2014, but increasing to 6.3% in 2015. The decline was primarily attributed to serotypes 7F and 19A, and the proportional increase to serotype 3. Similar trends were noted for bacteremic and non-bacteremic CAPSpn. Serious outcomes such as 30-day mortality, intensive care unit admission, and requirement for mechanical ventilation were prominent in CAPSpn and IPD cases, but remained unchanged over the study years. Herd immunity afforded primarily by serotypes 7F and 19A appears to be partly masked by a concomitant proportional increase of serotype 3. Despite evidence of herd immunity, these PCV13 serotypes remain persistent in Canadian adults hospitalized with CAPSpn, and represent between 5 and 10% of all CAP in this patient population.</description><identifier>ISSN: 0264-410X</identifier><identifier>EISSN: 1873-2518</identifier><identifier>DOI: 10.1016/j.vaccine.2019.05.003</identifier><identifier>PMID: 31345638</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Adult ; Adults ; Age ; Antibiotics ; Antigens ; Blood culture ; Burden ; Children ; Clinical outcomes ; Communities ; Community-acquired pneumonia (CAP) ; Culture ; Disease ; Disease prevention ; Herd immunity ; Hospitalization ; Immunity ; Immunization ; Influenza ; Laboratories ; Masking ; Mechanical ventilation ; Mortality ; PCV13 ; Pneumococcal vaccine ; Pneumonia ; Serotype ; Serotypes ; Sputum ; Streptococcus infections ; Streptococcus pneumoniae ; Surveillance ; Urine ; Vaccines ; Ventilation</subject><ispartof>Vaccine, 2019-08, Vol.37 (36), p.5466-5473</ispartof><rights>2019 The Authors</rights><rights>Copyright © 2019 The Authors. 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Serotype was assigned using Quellung reaction, PCR, or UADPCV13. Of 6687 CAP cases where a test was performed, S. pneumoniae positivity decreased from 15.9% in 2011 to 8.8% in 2014, but increased to 12.9% in 2015. CAPSpn attributed to PCV13 serotypes followed a similar trend, dropping from 8.3% in 2010 to 4.6% in 2014, but increasing to 6.3% in 2015. The decline was primarily attributed to serotypes 7F and 19A, and the proportional increase to serotype 3. Similar trends were noted for bacteremic and non-bacteremic CAPSpn. Serious outcomes such as 30-day mortality, intensive care unit admission, and requirement for mechanical ventilation were prominent in CAPSpn and IPD cases, but remained unchanged over the study years. Herd immunity afforded primarily by serotypes 7F and 19A appears to be partly masked by a concomitant proportional increase of serotype 3. Despite evidence of herd immunity, these PCV13 serotypes remain persistent in Canadian adults hospitalized with CAPSpn, and represent between 5 and 10% of all CAP in this patient population.</description><subject>Adult</subject><subject>Adults</subject><subject>Age</subject><subject>Antibiotics</subject><subject>Antigens</subject><subject>Blood culture</subject><subject>Burden</subject><subject>Children</subject><subject>Clinical outcomes</subject><subject>Communities</subject><subject>Community-acquired pneumonia (CAP)</subject><subject>Culture</subject><subject>Disease</subject><subject>Disease prevention</subject><subject>Herd immunity</subject><subject>Hospitalization</subject><subject>Immunity</subject><subject>Immunization</subject><subject>Influenza</subject><subject>Laboratories</subject><subject>Masking</subject><subject>Mechanical ventilation</subject><subject>Mortality</subject><subject>PCV13</subject><subject>Pneumococcal vaccine</subject><subject>Pneumonia</subject><subject>Serotype</subject><subject>Serotypes</subject><subject>Sputum</subject><subject>Streptococcus infections</subject><subject>Streptococcus pneumoniae</subject><subject>Surveillance</subject><subject>Urine</subject><subject>Vaccines</subject><subject>Ventilation</subject><issn>0264-410X</issn><issn>1873-2518</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFkk9vEzEQxRcEoqHwEUAjcUkPG_xnd-PtBVURlEpVgwggbpbXO0ucZtdb25sq_fR1SJoDF06W7N8bv5l5SfKOkgkltPi4mmyU1qbDCSO0nJB8Qgh_noyomPKU5VS8SEaEFVmaUfL7JHnt_YoQknNavkpOOOVZXnAxepYsgsM-WG21Hjz0HQ6t7YxC8Ohs2PYIHIyHVvlb0_2Bb7NflKct1kYFrGGJrgbTtkNnwhZMBzPVqfjWgaqHdfCwtL43Qa3NQ6TvTViCtk-40neDcfH--Os5XIAPQ72FxtkWwhJhgc7Y6Gw-hKhED4vBbdCs16rTCOPFfHEGNxjurbsF2_yVHD3sjT2oYGwHDj0qp5dHejy7-n5z9iZ52ai1x7eH8zT5-eXzj9nX9Hp-eTW7uE51lpGQMtqUhHJWVIKKDCsu8lIwnCpaiKrhZVWhxmzKm6IkU0oyZJkSKArNRVVUuuCnyXhft3f2bkAfZGu8xl0fGPuTjBX5tGAkKyP64R90ZQfXRXc7qiwZzxiNVL6ntLPeO2xk70yr3FZSIncRkSt5iIjcRUSSXMaIRN37Q_Whins8qp4yEYFPewDjODYGnfTaYJx2HZelg6yt-c8XjxEr02o</recordid><startdate>20190823</startdate><enddate>20190823</enddate><creator>LeBlanc, Jason J.</creator><creator>ElSherif, May</creator><creator>Ye, Lingyun</creator><creator>MacKinnon-Cameron, Donna</creator><creator>Ambrose, Ardith</creator><creator>Hatchette, Todd F.</creator><creator>Lang, Amanda L.S.</creator><creator>Gillis, Hayley D.</creator><creator>Martin, Irene</creator><creator>Demczuk, Walter</creator><creator>Andrew, Melissa K.</creator><creator>Boivin, Guy</creator><creator>Bowie, William</creator><creator>Green, Karen</creator><creator>Johnstone, Jennie</creator><creator>Loeb, Mark</creator><creator>McCarthy, Anne E.</creator><creator>McGeer, Allison</creator><creator>Semret, Makeda</creator><creator>Trottier, Sylvie</creator><creator>Valiquette, Louis</creator><creator>Webster, Duncan</creator><creator>McNeil, Shelly A.</creator><general>Elsevier Ltd</general><general>Elsevier Limited</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7RV</scope><scope>7T2</scope><scope>7T5</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88C</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0R</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>M2O</scope><scope>M7N</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0593-0357</orcidid><orcidid>https://orcid.org/0000-0003-2315-5390</orcidid></search><sort><creationdate>20190823</creationdate><title>Streptococcus pneumoniae serotype 3 is masking PCV13-mediated herd immunity in Canadian adults hospitalized with community acquired pneumonia: A study from the Serious Outcomes Surveillance (SOS) Network of the Canadian immunization research Network (CIRN)</title><author>LeBlanc, Jason J. ; ElSherif, May ; Ye, Lingyun ; MacKinnon-Cameron, Donna ; Ambrose, Ardith ; Hatchette, Todd F. ; Lang, Amanda L.S. ; Gillis, Hayley D. ; Martin, Irene ; Demczuk, Walter ; Andrew, Melissa K. ; Boivin, Guy ; Bowie, William ; Green, Karen ; Johnstone, Jennie ; Loeb, Mark ; McCarthy, Anne E. ; McGeer, Allison ; Semret, Makeda ; Trottier, Sylvie ; Valiquette, Louis ; Webster, Duncan ; McNeil, Shelly A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c440t-21f901326b8184eb385982e7a168bf39bbece473f6907104e24a8e86c38b6bc63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adult</topic><topic>Adults</topic><topic>Age</topic><topic>Antibiotics</topic><topic>Antigens</topic><topic>Blood culture</topic><topic>Burden</topic><topic>Children</topic><topic>Clinical outcomes</topic><topic>Communities</topic><topic>Community-acquired pneumonia (CAP)</topic><topic>Culture</topic><topic>Disease</topic><topic>Disease prevention</topic><topic>Herd immunity</topic><topic>Hospitalization</topic><topic>Immunity</topic><topic>Immunization</topic><topic>Influenza</topic><topic>Laboratories</topic><topic>Masking</topic><topic>Mechanical ventilation</topic><topic>Mortality</topic><topic>PCV13</topic><topic>Pneumococcal vaccine</topic><topic>Pneumonia</topic><topic>Serotype</topic><topic>Serotypes</topic><topic>Sputum</topic><topic>Streptococcus infections</topic><topic>Streptococcus pneumoniae</topic><topic>Surveillance</topic><topic>Urine</topic><topic>Vaccines</topic><topic>Ventilation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>LeBlanc, Jason J.</creatorcontrib><creatorcontrib>ElSherif, May</creatorcontrib><creatorcontrib>Ye, Lingyun</creatorcontrib><creatorcontrib>MacKinnon-Cameron, Donna</creatorcontrib><creatorcontrib>Ambrose, Ardith</creatorcontrib><creatorcontrib>Hatchette, Todd F.</creatorcontrib><creatorcontrib>Lang, Amanda L.S.</creatorcontrib><creatorcontrib>Gillis, Hayley D.</creatorcontrib><creatorcontrib>Martin, Irene</creatorcontrib><creatorcontrib>Demczuk, Walter</creatorcontrib><creatorcontrib>Andrew, Melissa K.</creatorcontrib><creatorcontrib>Boivin, Guy</creatorcontrib><creatorcontrib>Bowie, William</creatorcontrib><creatorcontrib>Green, Karen</creatorcontrib><creatorcontrib>Johnstone, Jennie</creatorcontrib><creatorcontrib>Loeb, Mark</creatorcontrib><creatorcontrib>McCarthy, Anne E.</creatorcontrib><creatorcontrib>McGeer, Allison</creatorcontrib><creatorcontrib>Semret, Makeda</creatorcontrib><creatorcontrib>Trottier, Sylvie</creatorcontrib><creatorcontrib>Valiquette, Louis</creatorcontrib><creatorcontrib>Webster, Duncan</creatorcontrib><creatorcontrib>McNeil, Shelly A.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Nursing &amp; 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Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Consumer Health Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Vaccine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>LeBlanc, Jason J.</au><au>ElSherif, May</au><au>Ye, Lingyun</au><au>MacKinnon-Cameron, Donna</au><au>Ambrose, Ardith</au><au>Hatchette, Todd F.</au><au>Lang, Amanda L.S.</au><au>Gillis, Hayley D.</au><au>Martin, Irene</au><au>Demczuk, Walter</au><au>Andrew, Melissa K.</au><au>Boivin, Guy</au><au>Bowie, William</au><au>Green, Karen</au><au>Johnstone, Jennie</au><au>Loeb, Mark</au><au>McCarthy, Anne E.</au><au>McGeer, Allison</au><au>Semret, Makeda</au><au>Trottier, Sylvie</au><au>Valiquette, Louis</au><au>Webster, Duncan</au><au>McNeil, Shelly A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Streptococcus pneumoniae serotype 3 is masking PCV13-mediated herd immunity in Canadian adults hospitalized with community acquired pneumonia: A study from the Serious Outcomes Surveillance (SOS) Network of the Canadian immunization research Network (CIRN)</atitle><jtitle>Vaccine</jtitle><addtitle>Vaccine</addtitle><date>2019-08-23</date><risdate>2019</risdate><volume>37</volume><issue>36</issue><spage>5466</spage><epage>5473</epage><pages>5466-5473</pages><issn>0264-410X</issn><eissn>1873-2518</eissn><abstract>•The proportion of CAP attributed to S. pneumoniae declined from 2010 to 2014, but increased in 2015.•PCV13 serotypes in bacteremic and non-bacteremic pneumococcal CAP mirrored trends seen for S. pneumoniae positivity.•Herd immunity afforded by serotypes 7F and 19A was partly masked by a concomitant increase in the proportion of serotype 3.•The shift in serotype distribution over time was not accompanied by changes in patient demographics or serious outcomes.•Despite herd immunity, pneumococcal CAP and IPD remain substantial cause of morbidity and mortality in hospitalized adults. The 13-valent pneumococcal conjugate vaccine (PCV13) was recently shown to be effective against PCV13-type invasive pneumococcal disease (IPD) and pneumococcal community acquired pneumonia (CAPSpn) in healthy adults aged ≥65 years, prompting many countries to re-assess adult immunization. In Canada, the potential benefits of adult PCV13 immunization were unclear given anticipated herd immunity from PCV13 childhood immunization introduced since 2010. This study describes the serotype distribution and clinical outcomes of Canadian adults aged ≥16 years, who were hospitalized with CAPSpn and IPD from 2010 to 2015. Active surveillance for CAP and IPD was performed in adult hospitals across five Canadian provinces. IPD was identified when Streptococcus pneumoniae was isolated from sterile sites. Bacteremic and non-bacteremic CAPSpn were identified using blood culture, and sputum culture or PCV13-specific urine antigen detection (UADPCV13), respectively. Serotype was assigned using Quellung reaction, PCR, or UADPCV13. Of 6687 CAP cases where a test was performed, S. pneumoniae positivity decreased from 15.9% in 2011 to 8.8% in 2014, but increased to 12.9% in 2015. CAPSpn attributed to PCV13 serotypes followed a similar trend, dropping from 8.3% in 2010 to 4.6% in 2014, but increasing to 6.3% in 2015. The decline was primarily attributed to serotypes 7F and 19A, and the proportional increase to serotype 3. Similar trends were noted for bacteremic and non-bacteremic CAPSpn. Serious outcomes such as 30-day mortality, intensive care unit admission, and requirement for mechanical ventilation were prominent in CAPSpn and IPD cases, but remained unchanged over the study years. Herd immunity afforded primarily by serotypes 7F and 19A appears to be partly masked by a concomitant proportional increase of serotype 3. Despite evidence of herd immunity, these PCV13 serotypes remain persistent in Canadian adults hospitalized with CAPSpn, and represent between 5 and 10% of all CAP in this patient population.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>31345638</pmid><doi>10.1016/j.vaccine.2019.05.003</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-0593-0357</orcidid><orcidid>https://orcid.org/0000-0003-2315-5390</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 0264-410X
ispartof Vaccine, 2019-08, Vol.37 (36), p.5466-5473
issn 0264-410X
1873-2518
language eng
recordid cdi_proquest_miscellaneous_2265762049
source Elsevier ScienceDirect Journals
subjects Adult
Adults
Age
Antibiotics
Antigens
Blood culture
Burden
Children
Clinical outcomes
Communities
Community-acquired pneumonia (CAP)
Culture
Disease
Disease prevention
Herd immunity
Hospitalization
Immunity
Immunization
Influenza
Laboratories
Masking
Mechanical ventilation
Mortality
PCV13
Pneumococcal vaccine
Pneumonia
Serotype
Serotypes
Sputum
Streptococcus infections
Streptococcus pneumoniae
Surveillance
Urine
Vaccines
Ventilation
title Streptococcus pneumoniae serotype 3 is masking PCV13-mediated herd immunity in Canadian adults hospitalized with community acquired pneumonia: A study from the Serious Outcomes Surveillance (SOS) Network of the Canadian immunization research Network (CIRN)
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