Evidence map›Paper›PMID 31594801›Full record

Observational studyThorax2020

Pneumococcal serotype trends, surveillance and risk factors in UK adult pneumonia, 2013-18.

Harry Pick, Priya Daniel, Chamira Rodrigo, Thomas Bewick, Deborah Ashton, Hannah Lawrence, Vadsala Baskaran, Rochelle C Edwards-Pritchard, Carmen Sheppard, Seyi D Eletu and 8 more

Open access · bronzeAbstract readObservational Study
PubMed Publisher
In one paragraph

Observational study in Thorax, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 2 pooled it
9.1field-weighted citation impact, top 2% of its field
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

59 citing papers in PubMed, 2 syntheses or guidelines pooled it, 112 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Observational
  15. Article
  16. Non-invasiveEuro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin · 2024
    Article
  17. Article
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 5 institutions in 1 country.

Harry PickDepartment of Respiratory Medicine, Nottingham University Hospitals NHS Trust, Nottingham, UK harry.pick@nhs.net.ORCID 0000-0002-1595-7919
Priya DanielRespiratory Medicine, University Hospitals of Derby and Burton NHS Foundation Trust, Derby, UK.
Chamira RodrigoDepartment of Respiratory Medicine, Nottingham University Hospitals NHS Trust, Nottingham, UK.
Thomas BewickRespiratory Medicine, University Hospitals of Derby and Burton NHS Foundation Trust, Derby, UK.
Deborah AshtonDepartment of Respiratory Medicine, Nottingham University Hospitals NHS Trust, Nottingham, UK.
Hannah LawrenceRespiratory Medicine, Nottingham University Hospitals NHS Trust, Nottingham, UK.
Vadsala BaskaranDepartment of Respiratory Medicine, Nottingham University Hospitals NHS Trust, Nottingham, UK.
Rochelle C Edwards-PritchardDivision of Respiratory Medicine, University of Nottingham, Nottingham, UK.ORCID 0000-0002-9248-2865
Carmen SheppardRespiratory and Vaccine Preventable Bacteria Reference Unit, Public Health England Colindale, London, UK.
Seyi D EletuRespiratory and Vaccine Preventable Bacteria Reference Unit, Public Health England Colindale, London, UK.
Samuel RoseRespiratory and Vaccine Preventable Bacteria Reference Unit, Public Health England Colindale, London, UK.ORCID 0000-0003-3848-6790
David LittRespiratory and Vaccine Preventable Bacteria Reference Unit, Public Health England Colindale, London, UK.
Norman K FryImmunisation and Countermeasures Division, Public Health England Colindale, London, UK.
Shamez LadhaniImmunisation and Countermeasures Division, Public Health England Colindale, London, UK.
Meera ChandTuberculosis, Acute Respiratory, Gastrointestinal, Emerging/Zoonotic Infections, Travel and Migrant Health Service (TARGET), Public Health England Colindale, London, UK.
Caroline TrotterDisease Dynamic Unit, Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.
Tricia M McKeeverDivision of Epidemiology and Public Health, University of Nottingham, Nottingham, UK.
Wei Shen LimDepartment of Respiratory Medicine, Nottingham University Hospitals NHS Trust, Nottingham, UK.
Public Health England · GBNottingham University Hospitals NHS Trust · GBUniversity Hospitals of Derby and Burton NHS Foundation Trust · GBUniversity of Nottingham · GBUniversity of Cambridge · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChanges over the last 5 years (2013-18) in the serotypes implicated in adult pneumococcal pneumonia and the patient groups associated with vaccine-type disease are largely unknown.

methodsWe conducted a population-based prospective cohort study of adults admitted to two large university hospitals with community-acquired pneumonia (CAP) between September 2013 and August 2018. Pneumococcal serotypes were identified using a novel 24-valent urinary monoclonal antibody assay and from blood cultures. Trends in incidence rates were compared against national invasive pneumococcal disease (IPD) data. Persons at risk of vaccine-type pneumonia (pneumococcal conjugate vaccine (PCV)13 and pneumococcal polysaccharide vaccine (PPV)23) were determined from multivariate analyses.

findingsOf 2934 adults hospitalised with CAP, 1075 (36.6%) had pneumococcal pneumonia. The annual incidence of pneumococcal pneumonia increased from 32.2 to 48.2 per 100 000 population (2013-18), predominantly due to increases in PCV13non7-serotype and non-vaccine type (NVT)-serotype pneumonia (annual incidence rate ratio 1.12, 95% CI 1.04 to 1.21 and 1.19, 95% CI 1.10 to 1.28, respectively). Incidence trends were broadly similar to IPD data. PCV13non7 (56.9% serotype 3) and PPV23non13 (44.1% serotype 8) serotypes were identified in 349 (32.5%) and 431 (40.1%) patients with pneumococcal pneumonia, respectively. PCV13-serotype pneumonia (dominated by serotype 3) was more likely in patients in the UK pneumococcal vaccination clinical risk group (adjusted OR (aOR) 1.73, 95% CI 1.31 to 2.28) while PPV23-serotype pneumonia was more likely in patients outside the clinical risk group (aOR 1.54, 95% CI 1.13 to 2.10).

interpretationThe incidence of pneumococcal CAP is increasing, predominantly due to NVT serotypes and serotype 3. PPV23-serotype pneumonia is more likely in adults outside currently identified clinical risk groups.

Indexed as

AdolescentAdultAgedAged, 80 and overCommunity-Acquired InfectionsFemaleHumansIncidenceMaleMiddle AgedPneumococcal VaccinesPneumonia, PneumococcalPopulation SurveillanceProspective StudiesRisk FactorsSerotypingPneumococcal VaccinesVaccines, Conjugatecommunity acquired pneumonianon-invasive pneumococcal diseasepneumococcal conjugate vaccinepneumococcal pneumoniapneumococcal polysaccharide vaccinereplacement serotypesrisk groupsStreptococcus pneumoniae

Identifiers

PMID31594801
OpenAlexW2979452343

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.