Evidence map›Paper›PMID 25569650›Full record

Observational studyMedicine2015

A cross-sectional observational study of pneumococcal carriage in children, their parents, and older adults following the introduction of the 7-valent pneumococcal conjugate vaccine.

Mainga Hamaluba, Rama Kandasamy, Susan Ndimah, Richard Morton, Marisa Caccamo, Hannah Robinson, Sarah Kelly, Aimee Field, Lily Norman, Emma Plested and 13 more

Abstract readObservational Study
In one paragraph

Observational study in Medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

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

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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

23 authors.

Mainga HamalubaFrom the Oxford Vaccine Group (MH, RK, SN, MC, HR, SK, AF, LN, EP, SAK, RL, TJ, MDS, AJP), Department of Paediatrics, University of Oxford, and the NIHR Oxford Biomedical Research Centre, Oxford; Guy's and St Thomas' National Health Service Foundation Trust (RM), London; Department of Primary Healthcare Sciences (BAVT), University of Oxford, Oxford; Northamptonshire Teaching Primary Care Trust (AZ), National Health Service, Northamptonshire; Centre for Statistics in Medicine (JH), University of Oxford, Oxford; Health Protection Services (PW), Public Health England; Division of Clinical Sciences (SNF, KAG, JH), St. George's University of London, London; and Nuffield Department of Clinical Medicine (DC), University of Oxford, Oxford, UK.
Rama Kandasamy
Susan Ndimah
Richard Morton
Marisa Caccamo
Hannah Robinson
Sarah Kelly
Aimee Field
Lily Norman
Emma Plested
Ben A V Thompson
Azhar Zafar
Simon A Kerridge
Rajeka Lazarus
Tessa John
Jane Holmes
Shannon N Fenlon
Katherine A Gould
Pauline Waight
Jason Hinds
Derrick Crook
Matthew D Snape
Andrew J Pollard

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Using nasopharyngeal carriage as a marker of vaccine impact, pneumococcal colonization and its relation to invasive disease were examined in children, their parents, and older adults in the United Kingdom following introduction of 7-valent pneumococcal conjugate vaccine (PCV7) and prior to 13-valent pneumococcal conjugate vaccine (PCV13).A cross-sectional observational study was conducted, collecting nasopharyngeal swabs from children aged 25 to 55 months who had previously received 3 doses of PCV7, their parents, and adults aged ≥65 years. Pneumococcal serotyping was conducted according to World Health Organization guidelines with nontypeable isolates further analyzed by molecular serotyping. A national invasive disease surveillance program was conducted throughout the corresponding period.Pneumococcus was isolated from 47% of children, 9% of parents, and 2.2% of older adults. For these groups, the percentage of serotypes covered by PCV7 were 1.5%, 0.0%, and 15.4%, with a further 20.1%, 44.4%, and 7.7% coverage added by those in PCV13. In each group, the percentage of disease due to serotypes covered by PCV7 were 1.0%, 7.4% and 5.1% with a further 65.3%, 42.1%, and 61.4% attributed to those in PCV13.The prevalence of carriage is the highest in children, with direct vaccine impact exemplified by low carriage and disease prevalence of PCV7 serotypes in vaccinated children, whereas the indirect effects of herd protection are implied by similar observations in unvaccinated parents and older adults.

Indexed as

AdultAgedChild, PreschoolCross-Sectional StudiesFemaleHumansMaleNasopharynxPneumococcal InfectionsSerogroupStreptococcus pneumoniaeVaccines, ConjugateVaccines, Conjugate

Identifiers

PMID25569650
PMCPMC4602851

What OpenQuestion holds

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LicenceCC BY-NC-SA
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Registered trials

None linked

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.