The effect of underlying clinical conditions on the risk of developing invasive pneumococcal disease in England

Albert Jan van Hoek*, Nick Andrews, Pauline A. Waight, Julia Stowe, Peter Gates, Robert George, Elizabeth Miller

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

208 Citations (Scopus)

Abstract

Objective: To inform national policy making on the use of the 13-valent pneumococcal vaccine among risk groups we estimated the increased risk of invasive pneumococcal disease (IPD) outcomes among clinical risk groups. Three years of post 7-valent pneumococcal conjugate vaccine (PCV7) data was included to investigate the herd protection effects. Methods: Over 22,000 IPD patients in England (March 2002-March 2009 - aged 2 and over) were linked to their hospitalisation records. The prevalence of risk factors in these patients was compared to the prevalence of risk factors in the general population. Results: There was an increased odds ratio (OR) for hospitalisation (OR 11.7 2-15 years; 7.6 16-64; 2.7 65+) and death (OR 2.4 2-15 years, 3.9 16-64, 1.2 65+) from IPD among risk group. The most important risk factors that predict IPD are chronic liver disease, immunosuppression, and chronic respiratory diseases. Herd protection effects due to introduction of the 7-valent vaccine were identical in both patient groups as shown by the similar decline in the proportion of IPD caused by PCV7 serotypes in risk and non-risk groups. Conclusions: There is a marked increased risk of IPD among those with certain clinical conditions, suggesting potential benefit from a targeted vaccination approach. However, the indirect protection from conjugate vaccination of children suggests PCV vaccination of high-risk groups may not provide substantial additional benefit once herd immunity takes effect.

Original languageEnglish
Pages (from-to)17-24
Number of pages8
JournalJournal of Infection
Volume65
Issue number1
DOIs
Publication statusPublished - Jul 2012

Bibliographical note

Funding Information:
This work was supported by the UK Department of Health Policy Research Programme , grant number: 039/0031 to AJvH and JS. The views expressed in the publication are those of the authors and not necessarily those of the Department of Health.

Funding Information:
AJvH, no conflict; NA, no conflict; PAW, no conflict; JS, no conflict; PG, no conflict; RG, has received assistance to attend scientific meetings from Wyeth (Pfizer) and GlaxoSmithKline, and his laboratory has received research funding from Wyeth (Pfizer) and GlaxoSmithKline; EM, no conflict.

Keywords

  • Hospitalisation
  • Invasive pneumococcal disease
  • Linkage
  • Mortality
  • Risk
  • Risk groups
  • Vaccination

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