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Article: Increase in incidence of invasive pneumococcal disease caused by serotype 3 in children eight years after the introduction of the pneumococcal conjugate vaccine in Hong Kong

TitleIncrease in incidence of invasive pneumococcal disease caused by serotype 3 in children eight years after the introduction of the pneumococcal conjugate vaccine in Hong Kong
Authors
Keywordsepidemiology
incidence
invasive pneumococcal disease
macrolide resistance
pneumococcal conjugate vaccine
Issue Date2019
PublisherTaylor & Francis Inc. The Journal's web site is located at http://www.tandfonline.com/khvi
Citation
Human Vaccines & Immunotherapeutics, 2019, v. 15 n. 2, p. 455-458 How to Cite?
AbstractThis study used several datasets of reported and serotyped invasive pneumococcal disease (IPD) cases to estimate vaccine and non-vaccine type incidence in Hong Kong children. Incidence was analyzed by four time periods to indicate pre-PCV (period 1, 1995–2004), private market only (period 2, 2006–2009), and following early (period 3, 2010–2014, mixed use of 7-, 10- and 13-valent vaccines) and more than five years (period 4, 2015–2017, 13-valent vaccine only) of routine implementation (since September 2009). IPD incidence decreased by 85% and 35% in aged < 2 years and aged 2 to < 5 years, respectively, from period 1 to period 4. This was due to a 97% reduction in the serotypes covered by 7-valent vaccine. In period 4, 59% of the disease was caused by serotype 3 and was largely attributed to an ermB positive, novel ST6011 clone. The finding corroborates an increasing body of evidence that the efficacy of the 13-valent vaccine against infection by this serotype is low.
Persistent Identifierhttp://hdl.handle.net/10722/264237
ISSN
2021 Impact Factor: 4.526
2020 SCImago Journal Rankings: 1.043
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorHo, PL-
dc.contributor.authorLaw, PYT-
dc.contributor.authorChiu, SSS-
dc.date.accessioned2018-10-22T07:51:44Z-
dc.date.available2018-10-22T07:51:44Z-
dc.date.issued2019-
dc.identifier.citationHuman Vaccines & Immunotherapeutics, 2019, v. 15 n. 2, p. 455-458-
dc.identifier.issn2164-5515-
dc.identifier.urihttp://hdl.handle.net/10722/264237-
dc.description.abstractThis study used several datasets of reported and serotyped invasive pneumococcal disease (IPD) cases to estimate vaccine and non-vaccine type incidence in Hong Kong children. Incidence was analyzed by four time periods to indicate pre-PCV (period 1, 1995–2004), private market only (period 2, 2006–2009), and following early (period 3, 2010–2014, mixed use of 7-, 10- and 13-valent vaccines) and more than five years (period 4, 2015–2017, 13-valent vaccine only) of routine implementation (since September 2009). IPD incidence decreased by 85% and 35% in aged < 2 years and aged 2 to < 5 years, respectively, from period 1 to period 4. This was due to a 97% reduction in the serotypes covered by 7-valent vaccine. In period 4, 59% of the disease was caused by serotype 3 and was largely attributed to an ermB positive, novel ST6011 clone. The finding corroborates an increasing body of evidence that the efficacy of the 13-valent vaccine against infection by this serotype is low.-
dc.languageeng-
dc.publisherTaylor & Francis Inc. The Journal's web site is located at http://www.tandfonline.com/khvi-
dc.relation.ispartofHuman Vaccines & Immunotherapeutics-
dc.rightsThis is an Accepted Manuscript of an article published by Taylor & Francis in Human Vaccines & Immunotherapeutics on 05 Oct 2018, available online: http://www.tandfonline.com/10.1080/21645515.2018.1526555-
dc.subjectepidemiology-
dc.subjectincidence-
dc.subjectinvasive pneumococcal disease-
dc.subjectmacrolide resistance-
dc.subjectpneumococcal conjugate vaccine-
dc.titleIncrease in incidence of invasive pneumococcal disease caused by serotype 3 in children eight years after the introduction of the pneumococcal conjugate vaccine in Hong Kong-
dc.typeArticle-
dc.identifier.emailHo, PL: plho@hku.hk-
dc.identifier.emailChiu, SSS: ssschiu@hku.hk-
dc.identifier.authorityHo, PL=rp00406-
dc.identifier.authorityChiu, SSS=rp00421-
dc.description.naturepostprint-
dc.identifier.doi10.1080/21645515.2018.1526555-
dc.identifier.scopuseid_2-s2.0-85054508144-
dc.identifier.hkuros295253-
dc.identifier.volume15-
dc.identifier.issue2-
dc.identifier.spage455-
dc.identifier.epage458-
dc.identifier.isiWOS:000461231000026-
dc.publisher.placeUnited States-
dc.identifier.issnl2164-5515-

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