Evidence map›Paper›PMID 31801542›Full record

ArticleBMC medicine2019

Determinants of high residual post-PCV13 pneumococcal vaccine-type carriage in Blantyre, Malawi: a modelling study.

J Lourenço, U Obolski, T D Swarthout, A Gori, N Bar-Zeev, D Everett, A W Kamng'ona, T S Mwalukomo, A A Mataya, C Mwansambo and 4 more

Abstract read
In one paragraph

Article in BMC medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
–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

35 citing papers in PubMed.

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  15. Streptococcus pneumoniae and other bacterial nasopharyngeal colonization seven years post-introduction of 13-valent pneumococcal conjugate vaccine in South African children.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2023
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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

14 authors.

J LourençoDepartment of Zoology, University of Oxford, Oxford, UK. jose.lourenco@zoo.ox.ac.uk.
U ObolskiSchool of Public Health, Tel Aviv University, Tel Aviv, Israel.
T D SwarthoutMalawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi.
A GoriNIHR Mucosal Pathogens Research Unit, Division of Infection & Immunity, University College London, London, UK.
N Bar-ZeevMalawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi.
D EverettMalawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi.
A W Kamng'onaDepartment of Biomedical Sciences, College of Medicine, University of Malawi, Blantyre, Malawi.
T S MwalukomoDepartment of Medicine, College of Medicine, University of Malawi, Blantyre, Malawi.
A A MatayaMalawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi.
C MwansamboMinistry of Health, Lilongwe, Malawi.
M BandaMinistry of Education, Blantyre, Malawi.
S GuptaDepartment of Zoology, University of Oxford, Oxford, UK.
N FrenchMalawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi.
R S HeydermanMalawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi.

Funding

Medical Research Council MR/N023129/1Wellcome Trust 106846/Z/15/Z
6 · The paper itself

Abstract

backgroundIn November 2011, Malawi introduced the 13-valent pneumococcal conjugate vaccine (PCV13) into the routine infant schedule. Four to 7 years after introduction (2015-2018), rolling prospective nasopharyngeal carriage surveys were performed in the city of Blantyre. Carriage of Streptococcus pneumoniae vaccine serotypes (VT) remained higher than reported in high-income countries, and impact was asymmetric across age groups.

methodsA dynamic transmission model was fit to survey data using a Bayesian Markov-chain Monte Carlo approach, to obtain insights into the determinants of post-PCV13 age-specific VT carriage.

resultsAccumulation of naturally acquired immunity with age and age-specific transmission potential were both key to reproducing the observed data. VT carriage reduction peaked sequentially over time, earlier in younger and later in older age groups. Estimated vaccine efficacy (protection against carriage) was 66.87% (95% CI 50.49-82.26%), similar to previous estimates. Ten-year projected vaccine impact (VT carriage reduction) among 0-9 years old was lower than observed in other settings, at 76.23% (CI 95% 68.02-81.96%), with sensitivity analyses demonstrating this to be mainly driven by a high local force of infection.

conclusionsThere are both vaccine-related and host-related determinants of post-PCV13 pneumococcal VT transmission in Blantyre with vaccine impact determined by an age-specific, local force of infection. These findings are likely to be generalisable to other Sub-Saharan African countries in which PCV impact on carriage (and therefore herd protection) has been lower than desired, and have implications for the interpretation of post-PCV carriage studies and future vaccination programs.

Indexed as

AgedChildChild, PreschoolCross-Sectional StudiesFemaleHumansInfantInfant, NewbornMalawiMaleModels, TheoreticalPneumococcal InfectionsPneumococcal VaccinesProspective StudiesStreptococcus pneumoniae13-valent pneumococcal vaccinePneumococcal VaccinesInterventionMalawiModellingpcv13Pneumococcus

Identifiers

PMID31801542
PMCPMC6894346

What OpenQuestion holds

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LicenceCC BY
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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.