Evidence map›Paper›PMID 41888721›Full record

ArticleBMC infectious diseases2026

Trends in invasive and non-invasive Streptococcus pneumoniae disease in adults hospitalised in Bristol and Bath: a retrospective cohort study, 2006-2022.

Robert Challen, Catherine Hyams, David Hettle, Zahin Amin-Chowdhury, Charli Grimes, Gabriella Ruffino, Rauri Conway, Robyn Heath, Paul North, Adam Malin and 6 more

Abstract read
In one paragraph

Article in BMC infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

16 authors.

Robert Challen *Engineering Mathematics, University of Bristol, Bristol, UK. rob.challen@bristol.ac.uk.
Catherine Hyams *Bristol Vaccine Centre, Schools of Cellular and Molecular Medicine and of Population Health Sciences, University of Bristol, Bristol, UK.
David HettleDepartment of Microbiology, Bristol Royal Infirmary, Upper Maudlin Street, Bristol, UK.
Zahin Amin-ChowdhuryImmunisation Department, UK Health Security Agency (UKHSA), London, UK.
Charli GrimesDepartment of Microbiology, Bristol Royal Infirmary, Upper Maudlin Street, Bristol, UK.
Gabriella RuffinoAcademic Respiratory Unit, Learning and Research Building, Southmead Hospital, Bristol, UK.
Rauri ConwayAcademic Respiratory Unit, Learning and Research Building, Southmead Hospital, Bristol, UK.
Robyn HeathBristol Vaccine Centre, Schools of Cellular and Molecular Medicine and of Population Health Sciences, University of Bristol, Bristol, UK.
Paul NorthDepartment of Microbiology, Bristol Royal Infirmary, Upper Maudlin Street, Bristol, UK.
Adam MalinDepartment of Respiratory Medicine, The Royal United Hospital, Bath, UK.
Nick A MaskellAcademic Respiratory Unit, Learning and Research Building, Southmead Hospital, Bristol, UK.
Philip WilliamsDepartment of Microbiology, Bristol Royal Infirmary, Upper Maudlin Street, Bristol, UK.
O Martin WilliamsDepartment of Microbiology, Bristol Royal Infirmary, Upper Maudlin Street, Bristol, UK.
Shamez N LadhaniImmunisation Department, UK Health Security Agency (UKHSA), London, UK.
Leon DanonEngineering Mathematics, University of Bristol, Bristol, UK.
Adam FinnBristol Vaccine Centre, Schools of Cellular and Molecular Medicine and of Population Health Sciences, University of Bristol, Bristol, UK.

Funding

AI programme of the Engineering and Physical Sciences Research Council EP/Y028392/1National Institute for Health Research ACF-2015-25-002
6 · The paper itself

Abstract

backgroundPneumococcal surveillance typically focuses on cases identified by positive microbiology and collects limited clinical data. The majority of pneumococcal studies in the literature focus on invasive respiratory disease. This study includes a cohort of all cause pneumococcal disease, including non-invasive disease and non-respiratory invasive disease with detailed clinical outcomes, allowing a more complete view of pneumococcal disease burden, and particularly meningitis cases.

methodsA longitudinal adult cohort of invasive and non-invasive pneumococcal disease inpatients in three hospitals between 2006 and 2022, was retrospectively collected. The demographics and outcomes of invasive and non-invasive hospitalised cases were compared. Features of invasive disease in different clinical presentations, particularly meningitis, were compared to invasive respiratory disease. Serotype distributions of different presentations in invasive disease were compared using bootstrap resampling.

resultsOut of a total 3719 all cause pneumococcal disease, 1419 cases (38.2%) were invasive respiratory disease. Non-invasive disease was seen in 2033 cases (54.7%). Non-invasive disease had a lower (but clinically substantial) 30 day case-fatality rate than invasive disease (11.7% versus 14.8%; P = 0.005), and similar lengths of stay in hospital. Among the 1686 invasive cases, 258 (15.3%) were outside the respiratory tract. The 172 cases presenting with meningitis were younger (54.9y vs. 66.8y; P < 0.001) than those with lower respiratory tract infection; and had high rates of intensive care admission (63.4% vs. LRTI 10.2%; P < 0.001). We found no evidence of a different serotype distribution between different clinical presentations.

conclusionsThere is a substantial burden of pneumococcal disease that is not represented by studies that focus on invasive respiratory disease, or by surveillance that focus only on culture positive disease alone. Outcomes are particularly poor in the case of meningitis, but non-invasive disease also has a high case fatality rate. Given the same serotypes are found in meningitis as invasive respiratory disease, we anticipate that the same vaccines that target respiratory disease should be relevant to the prevention of meningitis.

Indexed as

Pneumococcal InfectionsStreptococcus pneumoniaeAdultAgedAged, 80 and overFemaleHospitalizationHumansLongitudinal StudiesMaleMiddle AgedRetrospective StudiesSerogroupBacterial infectionSerotypesStreptococcus pneumoniae

Identifiers

PMID41888721
PMCPMC13141338

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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.