Evidence map›Paper›PMID 39394550›Full record

ArticleBMC medical informatics and decision making2024

A complex ePrescribing antimicrobial stewardship-based (ePAMS+) intervention for hospitals: mixed-methods feasibility trial results.

Christopher J Weir, Susan Hinder, Imad Adamestam, Rona Sharp, Holly Ennis, Andrew Heed, Robin Williams, Kathrin Cresswell, Omara Dogar, Sarah Pontefract and 10 more

Abstract read
In one paragraph

Article in BMC medical informatics and decision making, 2024. 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. Review
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

20 authors.

Christopher J WeirEdinburgh Clinical Trials Unit, Usher Institute, University of Edinburgh, Edinburgh, UK. Christopher.Weir@ed.ac.uk.ORCID http://orcid.org/0000-0002-6494-4903
Susan HinderUsher Institute, University of Edinburgh, Edinburgh, UK.ORCID http://orcid.org/0000-0001-8451-2027
Imad AdamestamEdinburgh Clinical Trials Unit, Usher Institute, University of Edinburgh, Edinburgh, UK.ORCID http://orcid.org/0000-0002-2873-3682
Rona SharpUsher Institute, University of Edinburgh, Edinburgh, UK.
Holly EnnisEdinburgh Clinical Trials Unit, Usher Institute, University of Edinburgh, Edinburgh, UK.
Andrew HeedNewcastle Upon Tyne Hospitals NHS Foundation Trust, Newcastle, UK.
Robin WilliamsInstitute for the Study of Science, Technology and Innovation, University of Edinburgh, Edinburgh, UK.ORCID http://orcid.org/0000-0002-9044-4611
Kathrin CresswellUsher Institute, University of Edinburgh, Edinburgh, UK.ORCID http://orcid.org/0000-0001-6634-9537
Omara DogarUsher Institute, University of Edinburgh, Edinburgh, UK.ORCID http://orcid.org/0000-0002-7122-8403
Sarah PontefractInstitute of Clinical Sciences, University of Birmingham, Birmingham, UK.ORCID http://orcid.org/0000-0002-0344-4075
Jamie ColemanInstitute of Clinical Sciences, University of Birmingham, Birmingham, UK.
Richard LilfordUniversity of Birmingham, Birmingham, UK.ORCID http://orcid.org/0000-0002-0634-984X
Neil WatsonNewcastle Upon Tyne Hospitals NHS Foundation Trust, Newcastle, UK.
Ann SleeUsher Institute, University of Edinburgh, Edinburgh, UK.ORCID http://orcid.org/0000-0002-9731-7041
Antony ChuterUsher Institute, University of Edinburgh, Edinburgh, UK.ORCID http://orcid.org/0000-0002-0646-5939
Jillian BeggsUsher Institute, University of Edinburgh, Edinburgh, UK.ORCID http://orcid.org/0000-0002-7591-3256
Sarah SlightSchool of Pharmacy, Newcastle University, Newcastle, UK.ORCID http://orcid.org/0000-0002-0339-846X
James MasonWarwick Medical School, University of Warwick, Warwick, UK.ORCID http://orcid.org/0000-0001-9210-4082
David W BatesHarvard Medical School, Boston, USA.
Aziz SheikhUsher Institute, University of Edinburgh, Edinburgh, UK.ORCID http://orcid.org/0000-0001-7022-3056

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAntibiotic resistant infections cause over 700,000 deaths worldwide annually. As antimicrobial stewardship (AMS) helps minimise the emergence of antibiotic resistance resulting from inappropriate use of antibiotics in healthcare, we developed ePAMS+ (ePrescribing-based Anti-Microbial Stewardship), an ePrescribing and Medicines Administration (EPMA) system decision-support tool complemented by educational, behavioural and organisational elements.

methodsWe conducted a non-randomised before-and-after feasibility trial, implementing ePAMS+ in two English hospitals using the Cerner Millennium EPMA system. Wards of several specialties were included. Patient participants were blinded to whether ePAMS+ was in use; prescribers were not. A mixed-methods evaluation aimed to establish: acceptability and usability of ePAMS+ and trial processes; feasibility of ePAMS+ implementation and quantitative outcome recording; and a Fidelity Index measuring the extent to which ePAMS+ was delivered as intended. Longitudinal semi-structured interviews of doctors, nurses and pharmacists, alongside non-participant observations, gathered qualitative data; we extracted quantitative prescribing data from the EPMA system. Normal linear modelling of the defined daily dose (DDD) of antibiotic per admission quantified its variability, to inform sample size calculations for a future trial of ePAMS+ effectiveness.

resultsThe research took place during the SARS-CoV-2 pandemic, from April 2021 to November 2022. 60 qualitative interviews were conducted (33 before ePAMS+ implementation, 27 after). 1,958 admissions (1,358 before ePAMS+ implementation; 600 after) included 24,884 antibiotic orders. Qualitative interviews confirmed that some aspects of ePAMS+ , its implementation and training were acceptable, while other features (e.g. enabling combinations of antibiotics to be prescribed) required further development. ePAMS+ uptake was low (28 antibiotic review records from 600 admissions; 0.047 records per admission), preventing full development of a Fidelity Index. Normal linear modelling of antibiotic DDD per admission showed a residual variance of 1.086 (log-transformed scale). Unavailability of indication data prevented measurement of some outcomes (e.g. number of antibiotic courses per indication).

conclusionsThis feasibility trial encountered unforeseen circumstances due to contextual factors and a global pandemic, highlighting the need for careful adaptation of complex intervention implementations to the local setting. We identified key refinements to ePAMS+ to support its wider adoption in clinical practice, requiring further piloting before a confirmatory effectiveness trial.

trial registrationISRCTN Registry ISRCTN13429325, 24 March 2022.

Indexed as

Antimicrobial StewardshipFeasibility StudiesAnti-Bacterial AgentsCOVID-19Decision Support Systems, ClinicalElectronic PrescribingFemaleHospitalsHumansMaleMiddle AgedAnti-Bacterial AgentsBacteriologyDecision supportHealth informaticsInfectious diseasesMicrobiology

Identifiers

PMID39394550
PMCPMC11470576

What OpenQuestion holds

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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.