The impact of 10-valent pneumococcal conjugate vaccine on the incidence of admissions to hospital with hypoxaemic and non-hypoxaemic pneumonia in Kenyan children.

Observational evidence suggests that pneumococcal conjugate vaccines (PCVs) are more effective at reducing the incidence of hypoxaemic pneumonia compared to non-hypoxaemic pneumonia. We examined the impact of 10-valent PCV (PCV10, Synflorix) on hypoxaemic pneumonia hospital admissions using data fro...

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Main Authors: Ilsa L Haeusler, E Wangeci Kagucia, Christian Bottomley, Mark Otiende, Joyce Nyiro, J Anthony G Scott
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2025-01-01
Series:PLOS Global Public Health
Online Access:https://doi.org/10.1371/journal.pgph.0004888
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author Ilsa L Haeusler
E Wangeci Kagucia
Christian Bottomley
Mark Otiende
Joyce Nyiro
J Anthony G Scott
author_facet Ilsa L Haeusler
E Wangeci Kagucia
Christian Bottomley
Mark Otiende
Joyce Nyiro
J Anthony G Scott
author_sort Ilsa L Haeusler
collection DOAJ
description Observational evidence suggests that pneumococcal conjugate vaccines (PCVs) are more effective at reducing the incidence of hypoxaemic pneumonia compared to non-hypoxaemic pneumonia. We examined the impact of 10-valent PCV (PCV10, Synflorix) on hypoxaemic pneumonia hospital admissions using data from an existing PCV impact study of clinical and radiographic pneumonia. PCV10 was introduced, with catch-up among children under 5 years, in the Kilifi Health and Demographic Surveillance System (KHDSS) in January 2011. We undertook an interrupted time-series (ITS) analysis using seasonally-adjusted segmented Poisson regression of hypoxaemic and non-hypoxaemic pneumonia, accounting for secular trends, from January 2007 to December 2019 among KHDSS residents aged 2-59 months. The median monthly crude incidence of hypoxaemic pneumonia per 100,000 person-years was 95 (IQR 80-139) in the pre-PCV10 period. Time-series regression estimated PCV10 introduction was associated with an increase in the incidence of hypoxaemic pneumonia in children aged 2-59 months (IRR 1.63, 95% CI 1.10-2.41), whereas it was associated with a decrease in the incidence of non-hypoxaemic pneumonia (IRR 0.61, 95% CI 0.48-0.77). Despite the consistent pneumonia surveillance and robust ITS analysis which accounted for pre-PCV10 secular trend and seasonality, the apparent association with hypoxaemic pneumonia is likely due to unmeasured time-varying confounders around the time of vaccine introduction, such as the epidemiology of other respiratory pathogens. This study highlights limitations in the analysis and interpretation of observational data in vaccine impact studies against pneumonia.
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spelling doaj-art-f6cb2d035cc64ad8a8a687e876564b682025-08-20T04:00:34ZengPublic Library of Science (PLoS)PLOS Global Public Health2767-33752025-01-0157e000488810.1371/journal.pgph.0004888The impact of 10-valent pneumococcal conjugate vaccine on the incidence of admissions to hospital with hypoxaemic and non-hypoxaemic pneumonia in Kenyan children.Ilsa L HaeuslerE Wangeci KaguciaChristian BottomleyMark OtiendeJoyce NyiroJ Anthony G ScottObservational evidence suggests that pneumococcal conjugate vaccines (PCVs) are more effective at reducing the incidence of hypoxaemic pneumonia compared to non-hypoxaemic pneumonia. We examined the impact of 10-valent PCV (PCV10, Synflorix) on hypoxaemic pneumonia hospital admissions using data from an existing PCV impact study of clinical and radiographic pneumonia. PCV10 was introduced, with catch-up among children under 5 years, in the Kilifi Health and Demographic Surveillance System (KHDSS) in January 2011. We undertook an interrupted time-series (ITS) analysis using seasonally-adjusted segmented Poisson regression of hypoxaemic and non-hypoxaemic pneumonia, accounting for secular trends, from January 2007 to December 2019 among KHDSS residents aged 2-59 months. The median monthly crude incidence of hypoxaemic pneumonia per 100,000 person-years was 95 (IQR 80-139) in the pre-PCV10 period. Time-series regression estimated PCV10 introduction was associated with an increase in the incidence of hypoxaemic pneumonia in children aged 2-59 months (IRR 1.63, 95% CI 1.10-2.41), whereas it was associated with a decrease in the incidence of non-hypoxaemic pneumonia (IRR 0.61, 95% CI 0.48-0.77). Despite the consistent pneumonia surveillance and robust ITS analysis which accounted for pre-PCV10 secular trend and seasonality, the apparent association with hypoxaemic pneumonia is likely due to unmeasured time-varying confounders around the time of vaccine introduction, such as the epidemiology of other respiratory pathogens. This study highlights limitations in the analysis and interpretation of observational data in vaccine impact studies against pneumonia.https://doi.org/10.1371/journal.pgph.0004888
spellingShingle Ilsa L Haeusler
E Wangeci Kagucia
Christian Bottomley
Mark Otiende
Joyce Nyiro
J Anthony G Scott
The impact of 10-valent pneumococcal conjugate vaccine on the incidence of admissions to hospital with hypoxaemic and non-hypoxaemic pneumonia in Kenyan children.
PLOS Global Public Health
title The impact of 10-valent pneumococcal conjugate vaccine on the incidence of admissions to hospital with hypoxaemic and non-hypoxaemic pneumonia in Kenyan children.
title_full The impact of 10-valent pneumococcal conjugate vaccine on the incidence of admissions to hospital with hypoxaemic and non-hypoxaemic pneumonia in Kenyan children.
title_fullStr The impact of 10-valent pneumococcal conjugate vaccine on the incidence of admissions to hospital with hypoxaemic and non-hypoxaemic pneumonia in Kenyan children.
title_full_unstemmed The impact of 10-valent pneumococcal conjugate vaccine on the incidence of admissions to hospital with hypoxaemic and non-hypoxaemic pneumonia in Kenyan children.
title_short The impact of 10-valent pneumococcal conjugate vaccine on the incidence of admissions to hospital with hypoxaemic and non-hypoxaemic pneumonia in Kenyan children.
title_sort impact of 10 valent pneumococcal conjugate vaccine on the incidence of admissions to hospital with hypoxaemic and non hypoxaemic pneumonia in kenyan children
url https://doi.org/10.1371/journal.pgph.0004888
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