Evidence map›Paper›PMID 39497193›Full record

ArticlePneumonia (Nathan Qld.)2024

Streptococcus pneumoniae serotype distribution in Bangladeshi under-fives with community-acquired pneumonia pre-10-valent pneumococcal conjugate vaccination.

Stefan M T Vestjens, Suzan P van Mens, Bob Meek, Tariq A Lalmahomed, Ben de Jong, Doli Goswami, Bart J M Vlaminckx, Dilruba Ahmed, Bartelt M de Jongh, Hubert P Endtz and 2 more

Abstract read
In one paragraph

Article in Pneumonia (Nathan Qld.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Stefan M T VestjensDepartment of Medical Microbiology & Immunology, St. Antonius Hospital, Nieuwegein, The Netherlands. smt.vest@gmail.com.
Suzan P van MensDepartment of Medical Microbiology & Immunology, St. Antonius Hospital, Nieuwegein, The Netherlands.
Bob MeekDepartment of Medical Microbiology & Immunology, St. Antonius Hospital, Nieuwegein, The Netherlands.
Tariq A LalmahomedScience Department, University College Roosevelt, Middelburg, Nieuwegein, The Netherlands.
Ben de JongDepartment of Medical Microbiology & Immunology, St. Antonius Hospital, Nieuwegein, The Netherlands.
Doli GoswamiInternational Center for Diarrhoeal Disease Research (icddr,b), Dhaka and Matlab, Bangladesh.
Bart J M VlaminckxDepartment of Medical Microbiology & Immunology, St. Antonius Hospital, Nieuwegein, The Netherlands.
Dilruba AhmedInternational Center for Diarrhoeal Disease Research (icddr,b), Dhaka and Matlab, Bangladesh.
Bartelt M de JonghDepartment of Medical Microbiology & Immunology, St. Antonius Hospital, Nieuwegein, The Netherlands.
Hubert P EndtzInternational Center for Diarrhoeal Disease Research (icddr,b), Dhaka and Matlab, Bangladesh.
W Abdullah BrooksInternational Center for Diarrhoeal Disease Research (icddr,b), Dhaka and Matlab, Bangladesh.
Ger T RijkersDepartment of Medical Microbiology & Immunology, St. Antonius Hospital, Nieuwegein, The Netherlands.

Funding

Sanofi Pasteur WHO Universal Trial Number U1111-1117-7316
6 · The paper itself

Abstract

backgroundStreptococcus pneumoniae is the most frequent causative pathogen of bacterial pneumonia in children worldwide. Bangladesh introduced the 10-valent pneumococcal conjugate vaccine (PCV10) in their national immunization program for infants in 2015. We assessed its potential coverage in under-fives with community-acquired pneumonia (CAP) in the years before PCV10 was introduced.

methodsA total of 1502 childhood pneumonia cases (< 5 year olds living in the urban section Kamalapur, Dhaka) were enrolled between 2011 and 2013. Acute phase and late (convalescent) serum samples were collected from 1380 cases. Serotype-specific pneumococcal antibody concentrations were measured using a 25-plex immunoassay panel. Pneumococcal CAP was diagnosed based on a serotype-specific pneumococcal antibody response.

resultsS. pneumoniae was serologically identified as causative pathogen in 406/1380 (29%) cases. The five most prevalent serotypes were (in descending order) 11A, 22F, 3, 2 and 19F. Based on the percentage of pneumonia cases associated with PCV10 vaccine types, the potential PCV10 coverage was 29% (116/406).

conclusionsIn almost a third of the studied cases S. pneumoniae was identified as a causative pathogen. Because of the characteristics of the immunoassay, this might well be a gross underestimation. Nevertheless, the potential PCV10-coverage was low. Given the high serotype diversity, the region might benefit greatly from a higher-coverage PCV or recombinant protein vaccine.

Indexed as

BangladeshChildrenPneumococcalPneumoniaSerotypes

Identifiers

PMID39497193
PMCPMC11536696

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.