Evidence map›Paper›PMID 41567260›Full record

ArticleOpen forum infectious diseases2026

Supervised Machine Learning to Identify Hospital Inpatients Needing a Change of Antibiotic Therapy in Real Time: Preclinical Diagnostic Evaluation and Feasibility Study.

P F Dutey-Magni, M Brown, S Harris, C Curtis, R Dobson, H Chowdhury, A Cawthorn, S De, N Stone, J Cooper and 1 more

Abstract read
In one paragraph

Article in Open forum infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

11 authors.

P F Dutey-MagniInstitute of Clinical Trials and Methodology, University College London, London, United Kingdom.ORCID https://orcid.org/0000-0002-8942-9836
M BrownInfection Department, University College London Hospitals NHS Foundation Trust, London, United Kingdom.ORCID https://orcid.org/0000-0001-7205-8947
S HarrisBiomedical Research Centre, University College London Hospitals NHS Foundation Trust, London, United Kingdom.ORCID https://orcid.org/0000-0002-4982-1374
C CurtisDepartment of Infection Sciences, King's College London NHS Foundation Trust, London, United Kingdom.
R DobsonInstitute of Health Informatics, University College London, London, United Kingdom.
H ChowdhuryInfection Department, University College London Hospitals NHS Foundation Trust, London, United Kingdom.
A CawthornAdvanced Research Computing Centre, University College London, London, United Kingdom.
S DeDepartment of Microbiology, Virology and Infection Control, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.
N StoneInfection Department, University College London Hospitals NHS Foundation Trust, London, United Kingdom.ORCID https://orcid.org/0000-0002-6887-7947
J CooperAdvanced Research Computing Centre, University College London, London, United Kingdom.ORCID https://orcid.org/0000-0001-6009-3542
L ShallcrossInstitute of Health Informatics, University College London, London, United Kingdom.ORCID https://orcid.org/0000-0003-1713-2555

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Postprescription review (PPR) by clinical microbiology/infectious diseases specialists is a proven intervention for optimizing antibiotic management in hospitals. However, hospitals lack sufficient staff to conduct PPR at scale. This study investigated the feasibility and diagnostic performance of supervised machine learning to monitor electronic medical records and prioritize PPR in real time. Methods: Over 2 years, infection specialists categorized PPR recommendations as recommendations to "stop," "change," or "continue" therapy at an acute hospital in London, United Kingdom. These labels (n = 2625) were linked to features generated from electronic patient records. Random forest, XGBoost, and C5 classifiers were trained before undergoing prospective evaluation in an unseen representative validation dataset (446 PPR decisions). The prespecified minimum predictive performance target was an area under the curve (AUC) of 0.75, with statistical power to detect an AUC <0.68 or >0.82. We then aggregated the validation dataset at the patient level (n = 358) and compared the clinical utility of targeted PPR using the classifier against unprioritized (random) PPR. Results: In the prospective validation set, 145 of 358 patients (41%) were recommended to change or stop treatment. The best-fitting classifier (random forest, cross-validation AUC, 0.74) achieved an AUC of 0.70 (95% confidence interval, .65-.75). If just the top 30% of patients receiving antibiotics could be reviewed, the classifier would help stop or change treatment in 68 of 145 patients requiring a change, compared with 43 of 145 if patients were selected at random. Conclusions: The prospective clinical evaluation demonstrated that the approach is feasible and achieves moderate predictive performance in real-world conditions.

Indexed as

antimicrobial stewardshipinfectious disease medicinemedication reviewsecondary caresupervised machine learning

Identifiers

PMID41567260
PMCPMC12817996

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Registered trials

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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.