Evidence map›Paper›PMID 39973904›Full record

ArticleJAC-antimicrobial resistance2025

Host-response testing with MeMed BV in community-acquired pneumonia: an economic evaluation from the UK NHS perspective.

Emily Gregg, Sara Graziadio, William Green, Daniela Afonso, Monica Garrett, Karina Watts, Deborah Watkins, Enitan D Carrol, Jonathan Cooke, Tim Felton

Abstract read
In one paragraph

Article in JAC-antimicrobial resistance, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
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

10 authors.

Emily GreggYork Health Economics Consortium (YHEC), University of York, York, UK.ORCID https://orcid.org/0009-0003-2969-793X
Sara GraziadioYork Health Economics Consortium (YHEC), University of York, York, UK.
William GreenYork Health Economics Consortium (YHEC), University of York, York, UK.
Daniela AfonsoYork Health Economics Consortium (YHEC), University of York, York, UK.ORCID https://orcid.org/0000-0002-0389-7912
Monica GarrettYork Health Economics Consortium (YHEC), University of York, York, UK.ORCID https://orcid.org/0000-0002-5802-3198
Karina WattsYork Health Economics Consortium (YHEC), University of York, York, UK.
Deborah WatkinsYork Health Economics Consortium (YHEC), University of York, York, UK.
Enitan D CarrolDepartment of Clinical Infection, Microbiology and Immunology, University of Liverpool Institute of Infection, Veterinary and Ecological Sciences, Liverpool, UK.
Jonathan CookeNIHR London In Vitro Diagnostics Co-operative, Division of Surgery, Department of Surgery and Cancer, Faculty of Medicine, Imperial College, London, UK.
Tim FeltonDivision of Immunology, Immunity to Infection and Respiratory Medicine, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Community-acquired pneumonia (CAP) remains a leading cause of hospital admissions and mortality. A novel host-response test, MeMed BV (MMBV), has been developed for discriminating between bacterial and viral infection that could improve the clinical management of CAP. Objectives: To evaluate the cost-effectiveness of using MMBV to guide antibiotic decisions in the clinical management of CAP in the UK. Methods: An economic model was developed to understand the incremental cost per person associated with the implementation of MMBV from the UK NHS perspective. A qualitative care pathway analysis was performed to inform the standard of care (SOC) and SOC plus MMBV (SOC + MMBV) clinical pathways captured in the model. Results: In the base case analysis, the SOC + MMBV strategy for a hypothetical cohort of 1000 patients (adults and children modelled independently) presenting to the emergency department with suspected CAP was estimated to provide total cost savings of £134 018 and £105 750 for adults and children, respectively. Cost savings were associated with reductions in total antibiotic treatment, the number of patients receiving additional diagnostic tests, and hospital admissions. Deterministic sensitivity analysis revealed that the specificity of SOC + MMBV and sensitivity of the SOC were primary drivers of the cost model for adults, whereas the specificity of SOC and SOC + MMBV were primary drivers for paediatrics. Conclusions: Overall, the model predicts that the introduction of SOC + MMBV has the potential to be cost-saving and promote antimicrobial stewardship for both adult and paediatric CAP patients.

Identifiers

PMID39973904
PMCPMC11836884

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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.