Evidence map›Paper›PMID 38842487›Full record

ArticleThe Journal of antimicrobial chemotherapy2024

The cost-effectiveness of procalcitonin for guiding antibiotic prescribing in individuals hospitalized with COVID-19: part of the PEACH study.

Edward J D Webb, Daniel Howdon, Rebecca Bestwick, Natalie King, Jonathan A T Sandoe, Joanne Euden, Detelina Grozeva, Robert West, Philip Howard, Neil Powell and 18 more

Abstract read
In one paragraph

Article in The Journal of antimicrobial chemotherapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Observational
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

28 authors.

Edward J D WebbLeeds Institute for Health Sciences, University of Leeds, Leeds, UK.ORCID 0000-0001-7918-839X
Daniel HowdonLeeds Institute for Health Sciences, University of Leeds, Leeds, UK.
Rebecca BestwickLeeds Institute for Health Sciences, University of Leeds, Leeds, UK.
Natalie KingLeeds Institute for Health Sciences, University of Leeds, Leeds, UK.
Jonathan A T SandoeHealthcare Associated Infection Group, Leeds Institute of Medical Research, University of Leeds, Leeds, UK.ORCID 0000-0003-0193-8677
Joanne EudenCentre for Trials Research, College of Biomedical and Life Sciences, Cardiff University, Cardiff, UK.ORCID 0000-0002-2844-6878
Detelina GrozevaCentre for Trials Research, College of Biomedical and Life Sciences, Cardiff University, Cardiff, UK.ORCID 0000-0003-3239-8415
Robert WestLeeds Institute for Health Sciences, University of Leeds, Leeds, UK.
Philip HowardHealthcare Associated Infection Group, Leeds Institute of Medical Research, University of Leeds, Leeds, UK.ORCID 0000-0002-5096-0240
Neil PowellPharmacy Department, Royal Cornwall Hospital, Royal Cornwall Hospitals NHS Foundation Trust, Truro TR1 3LJ, UK.ORCID 0000-0002-6113-9810
Mahableshwar AlburSevern Infectious Sciences, Southmead Hospital, North Bristol NHS Trust, Bristol BS10 5NB, UK.
Stuart BondMedicines Optimisation and Pharmacy Services, Pinderfields Hospital, Mid Yorkshire Teaching NHS Trust, Wakefield WF1 4DG, UK.ORCID 0000-0001-9640-2474
Lucy Brookes-HowellCentre for Trials Research, College of Biomedical and Life Sciences, Cardiff University, Cardiff, UK.
Paul DarkDivision of Immunology, Faculty of Biology, Medicine and Health, Immunity to Infection and Respiratory Medicine, School of Biological Sciences, University of Manchester, Manchester M13 9PL, UK.ORCID 0000-0003-3309-0164
Thomas HellyerPerioperative and Critical Care Department, Institute of Transplantation, Freeman Hospital, Newcastle upon Tyne Hospital NHS Foundation Trust, Newcastle upon Tyne NE7 7DN, UK.
Martin LlewelynGlobal Health and Infection, Brighton and Sussex Medical School, University of Sussex, Brighton BN1 9PS, UK.
Iain J McCullaghPerioperative and Critical Care Department, Institute of Transplantation, Freeman Hospital, Newcastle upon Tyne Hospital NHS Foundation Trust, Newcastle upon Tyne NE7 7DN, UK.
Margaret OgdenPublic and Patient Involvement Representative, NIHR, London SW1A 2NS, UK.
Philip PallmannCentre for Trials Research, College of Biomedical and Life Sciences, Cardiff University, Cardiff, UK.
Helena ParsonsDepartment of Microbiology, Laboratory Medicine, Northern General Hospital, Sheffield Teaching Hospital NHS Foundation Trust, Sheffield S5 7AU, UK.
David PartridgeDepartment of Microbiology, Laboratory Medicine, Northern General Hospital, Sheffield Teaching Hospital NHS Foundation Trust, Sheffield S5 7AU, UK.ORCID 0000-0002-0417-2016
Dominick ShawDepartment of Respiratory Sciences, University of Leicester, Leicester, UK.
Tamas SzakmanyRoyal Gwent Hospital, Aneurin Bevan University Health Board, Newport, UK.
Stacy ToddTropical and Infectious Disease Unit, The Royal Liverpool and Broadgreen University Hospitals NHS Trust, Liverpool, UK.
Emma Thomas-JonesCentre for Trials Research, College of Biomedical and Life Sciences, Cardiff University, Cardiff, UK.
Enitan D CarrolDepartment of Clinical Infection, Microbiology and Immunology, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK.
Bethany ShinkinsLeeds Institute for Health Sciences, University of Leeds, Leeds, UK.
PEACH Study Group

Funding

HCRW_National Institute for Health NIHR132254
6 · The paper itself

Abstract

backgroundMany hospitals introduced procalcitonin (PCT) testing to help diagnose bacterial coinfection in individuals with COVID-19, and guide antibiotic decision-making during the COVID-19 pandemic in the UK.

objectivesEvaluating cost-effectiveness of using PCT to guide antibiotic decisions in individuals hospitalized with COVID-19, as part of a wider research programme.

methodsRetrospective individual-level data on patients hospitalized with COVID-19 were collected from 11 NHS acute hospital Trusts and Health Boards from England and Wales, which varied in their use of baseline PCT testing during the first COVID-19 pandemic wave. A matched analysis (part of a wider analysis reported elsewhere) created groups of patients whose PCT was/was not tested at baseline. A model was created with combined decision tree/Markov phases, parameterized with quality-of-life/unit cost estimates from the literature, and used to estimate costs and quality-adjusted life years (QALYs). Cost-effectiveness was judged at a £20 000/QALY threshold. Uncertainty was characterized using bootstrapping.

resultsPeople who had baseline PCT testing had shorter general ward/ICU stays and spent less time on antibiotics, though with overlap between the groups' 95% CIs. Those with baseline PCT testing accrued more QALYs (8.76 versus 8.62) and lower costs (£9830 versus £10 700). The point estimate was baseline PCT testing being dominant over no baseline testing, though with uncertainty: the probability of cost-effectiveness was 0.579 with a 1 year horizon and 0.872 with a lifetime horizon.

conclusionsUsing PCT to guide antibiotic therapy in individuals hospitalized with COVID-19 is more likely to be cost-effective than not, albeit with uncertainty.

Indexed as

Anti-Bacterial AgentsCost-Benefit AnalysisCOVID-19ProcalcitoninAdultAgedBacterial InfectionsCOVID-19 Drug TreatmentFemaleHospitalizationHumansMaleMiddle AgedQuality-Adjusted Life YearsRetrospective StudiesSARS-CoV-2Anti-Bacterial AgentsProcalcitonin

Identifiers

PMID38842487
PMCPMC11290882

What OpenQuestion holds

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LicenceCC BY
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.