Evidence map›Paper›PMID 39367515›Full record

ArticlePneumonia (Nathan Qld.)2024

Radiographically confirmed pneumonia in Malawian children and associated pneumococcal carriage after introduction of the 13-valent pneumococcal conjugate vaccine.

Grace Mzumara, James Chirombo, Todd D Swarthout, Naor Bar-Zeev, Philliness Prisca Harawa, Mohamed Sanusi Jalloh, Amir Kirolos, Victoria Mukhula, Laura Newberry, Olawale Ogunlade and 4 more

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Article in Pneumonia (Nathan Qld.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.

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

What it found

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Grace MzumaraMalawi-Liverpool Wellcome Programme, Blantyre, Malawi. gmzumara@mlw.mw.
James ChiromboMalawi-Liverpool Wellcome Programme, Blantyre, Malawi.
Todd D SwarthoutDepartment of Infection, Division of Infection and Immunity, University College London, London, UK.
Naor Bar-ZeevMalawi-Liverpool Wellcome Programme, Blantyre, Malawi.
Philliness Prisca HarawaMalawi-Liverpool Wellcome Programme, Blantyre, Malawi.
Mohamed Sanusi JallohLiverpool School of Tropical Medicine, Liverpool, UK.
Amir KirolosUniversity of Liverpool, Liverpool, UK.
Victoria MukhulaMalawi-Liverpool Wellcome Programme, Blantyre, Malawi.
Laura NewberryMalawi-Liverpool Wellcome Programme, Blantyre, Malawi.
Olawale OgunladeLiverpool School of Tropical Medicine, Liverpool, UK.
Richard WachepaMalawi-Liverpool Wellcome Programme, Blantyre, Malawi.
Neil FrenchUniversity of Liverpool, Liverpool, UK.
Robert S HeydermanDepartment of Infection, Division of Infection and Immunity, University College London, London, UK.
Pui-Ying Iroh TamMalawi-Liverpool Wellcome Programme, Blantyre, Malawi.

Funding

Bill and Melinda Gates Foundation OPP1117653National Institute for Health and Care Research 16/136/46Wellcome TrustWellcome Trust WT091909/B/10/ZWorld Health Organization 001
6 · The paper itself

Abstract

backgroundThe 13-valent pneumococcal conjugate vaccine (PCV-13) was introduced in Malawi in 2011 with an expected impact of reducing pneumococcal pneumonia in children. We aimed to describe clinical characteristics and nasopharyngeal (NP) carriage of pneumococcus by serotype in children hospitalized with primary end-point pneumonia (PEP) between 2013 and 19 after the introduction of PCV-13.

methodsWe conducted a secondary analysis of children aged under-5-years hospitalized with acute respiratory illness (ARI) in Malawi. Chest radiographs conducted at admission were read by two independent clinicians according to WHO criteria for PEP, and a third reviewer resolved discordant diagnoses. NP swab specimens were processed and Streptococcus pneumoniae growth was serotyped. Multivariable regression analysis was conducted to assess the association between clinical characteristics, NP serotypes, and PEP.

resultsWe had complete radiographic and NP serotype data for 500 children, of which 54 isolates were vaccine-type (VT) (10.8%), 165 were non-VT (NVT; 33.0%), and 281 had no pneumococcal growth (56.2%). Among these, 176 (35.2%) had PEP on chest x-ray. Among those with PEP, pneumococcal carriage was documented in 43.8% of cases, and VT serotypes accounted for 10.8%. For children with PEP, we found no association between clinical characteristics and carrying either VT, NVT, or no pneumococcus.

conclusionCarriage of S. pneumoniae remains high among children hospitalized with ARI in Malawi, but children with VT carriage were no more likely to have PEP than children carrying no pneumococcus or those with NVT carriage. There were no differences in clinical characteristics between those carrying VT, NVT, or no pneumococcus.

Indexed as

ChildPneumococcal conjugate vaccineRadiographic pneumoniaRespiratory illnessSerotypesSub-Saharan Africa

Identifiers

PMID39367515
PMCPMC11452976

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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.