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. 2011;6(12):e28435.
doi: 10.1371/journal.pone.0028435. Epub 2011 Dec 2.

Using the indirect cohort design to estimate the effectiveness of the seven valent pneumococcal conjugate vaccine in England and Wales

Affiliations

Using the indirect cohort design to estimate the effectiveness of the seven valent pneumococcal conjugate vaccine in England and Wales

Nick Andrews et al. PLoS One. 2011.

Abstract

Background: The 7-valent pneumococcal conjugate vaccine (PCV-7) was introduced in the United Kingdom in 2006 with a 2, 3 and 13 month schedule, and has led to large decreases in invasive pneumococcal disease (IPD) caused by the vaccine serotypes in both vaccinated and unvaccinated cohorts. We estimated the effectiveness of PCV-7 against IPD.

Methods and findings: We used enhanced surveillance data, collated at the Health Protection Agency, on vaccine type (n = 153) and non vaccine type (n = 919) IPD cases eligible for PCV-7. The indirect cohort method, a case-control type design which uses non vaccine type cases as controls, was used to estimate effectiveness of various numbers of doses as well as for each vaccine serotype. Possible bias with this design, caused by differential serotype replacement in vaccinated and unvaccinated individuals, was estimated after deriving formulae to quantify the bias. The results showed good effectiveness, increasing from 56% (95% confidence interval (CI): -7-82) for a single dose given under one year of age to 93% (95% CI: 70-98) for two doses under one year of age plus a booster dose in the second year of life. Serotype specific estimates indicated higher effectiveness against serotypes 4, 14 and 18C and lower effectiveness against 6B. Under the assumption of complete serotype replacement by non vaccine serotypes in carriage, we estimated that effectiveness estimates may be overestimated by about 2 to 5%.

Conclusions: This study shows high effectiveness of PCV-7 under the reduced schedule used in the UK. This finding agrees with the large reductions seen in vaccine type IPD in recent years in England and Wales. The formulae derived to assess the bias of the indirect cohort method for PCV-7 can also be used when using the design for other vaccines that affect carriage such as the recently introduced 13 valent pneumococcal conjugate vaccine.

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Conflict of interest statement

Competing Interests: RB has performed contract research on behalf of the Health Protection Agency that was funded by Pfizer, GlaxoSmithKline, Sanofi Pasteur, and Merck. MS has received assistance to attend scientific meetings from Pfizer and GlaxoSmithKline and research funding from Pfizer and GlaxoSmithKline. RG has received support for conference attendance from Pfizer and GlaxoSmithKline, and his laboratory has received research funding from Pfizer and GlaxoSmithKline. SL has received assistance to attend scientific meetings from Pfizer and GlaxoSmithKline. This declaration does not alter the authors' adherence to all the PLoS ONE policies on sharing data and materials. None of the funding from Pfizer, GlaxoSmithKline, Sanofi Pasteur, or Merck was used specifically for this study.

Figures

Figure 1
Figure 1. Serotype distribution of IPD cases included in the study.
Enhanced surveillance serotyped IPD cases from England and Wales with known vaccination status from November 2006 to May 2010. Dark grey bars are PCV-7 serotypes and light grey bars non PCV-7 serotypes.
Figure 2
Figure 2. Assessment of bias when estimating VE with the indirect cohort design when there is complete serotype replacement.
VEBroome is observed vaccine effectiveness by the indirect cohort method, VEc is true vaccine effectiveness against carriage, VE is true vaccine effectiveness (combining effectiveness against carriage and IPD given carriage) and Pu is the proportion of carriage that is VT in the unvaccinated. The formula relating these quantities is VEBroome  =  1 – (1-VE)/ (1 + VEc Pu / (1-Pu)). Panel A) VE = 90%, panel B) VE = 70%.

References

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