Is It Time To Review The Vaccination Strategy To Protect Adults Against Invasive Pneumococcal Disease?


Journal

Irish medical journal
ISSN: 0332-3102
Titre abrégé: Ir Med J
Pays: Ireland
ID NLM: 0430275

Informations de publication

Date de publication:
14 03 2019
Historique:
entrez: 11 4 2019
pubmed: 11 4 2019
medline: 18 1 2020
Statut: epublish

Résumé

Pneumococcal conjugate vaccines (PCVs) have reduced the predominant serotypes causing invasive pneumococcal disease (IPD). We assessed the impact of the paediatric 7- and 13-valent pneumococcal conjugate vaccines (PCV7 and PCV13) among older adults. We compared serotype-specific incidence rates from 2007/08 to 2016/17, expressed as incidence rate ratios (IRR). Introducing PCV7 and PCV13 into the childhood immunisation programme resulted in a decline in these serotypes in adults ≥65 years of age, with PCV7 serotypes decreasing by 85% (IRR=0.11, 95%CI: 0.05-0.22, p<0.0001) and PCV13 serotypes not included in PCV7 (PCV13-7), decreasing by 9% (IRR=0.68, 95%CI: 0.40-1.16, p=0.134). However, there was a significant increase in serotypes only found in the 23-valent polysaccharide vaccine, PPV23-PCV13: IRR=2.57, 95%CI: 1.68-4.03, p<0.0001, and non-vaccine types (NVTs), IRR=3.33, 95%CI: 1.75-6.84, p=0.0001. The decline of IPD associated with PCV7/13 serotypes and the increase in PPV23-PCV13 serotypes indicates clear serotype replacement. Increasing PPV23 uptake could still reduce the burden of disease for this population.

Identifiants

pubmed: 30968681

Substances chimiques

Pneumococcal Vaccines 0
Vaccines, Conjugate 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

894

Commentaires et corrections

Type : CommentIn

Déclaration de conflit d'intérêts

HH has recently received research funds from Astellas and Pfizer, and has received lecture and other fees from Cepheid and Astellas. MCo and MMcE have received funding support from Pfizer. Additional funding has been provided through an unrestricted research grant from Pfizer (Ireland). The funders had no role in the collection, analysis, interpretation of data or in the writing of and decision to submit the article for publication.

Auteurs

M Corcoran (M)

The Irish Pneumococcal Reference Laboratory, Irish Meningitis and Sepsis Reference Laboratory, Temple Street Children’s University Hospital, Temple Street, Dublin 1, Ireland.

J Mereckiene (J)

Health Protection Surveillance Centre, Dublin, Gardiner Street, Dublin 1, Ireland.

S Murchan (S)

Health Protection Surveillance Centre, Dublin, Gardiner Street, Dublin 1, Ireland.

M McElligott (M)

The Irish Pneumococcal Reference Laboratory, Irish Meningitis and Sepsis Reference Laboratory, Temple Street Children’s University Hospital, Temple Street, Dublin 1, Ireland.
Department of Clinical Microbiology, the Royal College of Surgeons in Ireland, RCSI Education & Research Centre, Beaumont Hospital, Beaumont, Dublin 9, Ireland.

D ’Flanagan (D)

Health Protection Surveillance Centre, Dublin, Gardiner Street, Dublin 1, Ireland.

S Cotter (S)

Health Protection Surveillance Centre, Dublin, Gardiner Street, Dublin 1, Ireland.

R Cunney (R)

The Irish Pneumococcal Reference Laboratory, Irish Meningitis and Sepsis Reference Laboratory, Temple Street Children’s University Hospital, Temple Street, Dublin 1, Ireland.
Health Protection Surveillance Centre, Dublin, Gardiner Street, Dublin 1, Ireland.
Department of Microbiology, Temple Street Children’s University Hospital, Dublin 1, Ireland.

H Humphreys (H)

The Irish Pneumococcal Reference Laboratory, Irish Meningitis and Sepsis Reference Laboratory, Temple Street Children’s University Hospital, Temple Street, Dublin 1, Ireland.
Department of Clinical Microbiology, the Royal College of Surgeons in Ireland, RCSI Education & Research Centre, Beaumont Hospital, Beaumont, Dublin 9, Ireland.
Department of Microbiology, Beaumont Hospital, Beaumont, Dublin 9, Ireland.

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Classifications MeSH