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

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

Publication date: Oct 11, 2024

Antibiotic 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. We 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. The 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). This 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. ISRCTN Registry ISRCTN13429325, 24 March 2022.

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Concepts Keywords
Antibiotics Anti-Bacterial Agents
Daily Anti-Bacterial Agents
Deaths Antimicrobial Stewardship
Interviews Bacteriology
Isrctn13429325 COVID-19
Decision support
Electronic Prescribing
Feasibility Studies
Female
Health informatics
Hospitals
Humans
Infectious diseases
Male
Microbiology
Middle Aged

Semantics

Type Source Name
disease IDO intervention
disease MESH infections
disease IDO antibiotic resistance
pathway REACTOME Reproduction
disease MESH Infectious diseases
disease MESH stroke
disease MESH cancers
drug DRUGBANK Etoperidone
drug DRUGBANK Amoxicillin
disease IDO infection
drug DRUGBANK Tretamine
disease IDO replication
drug DRUGBANK Coenzyme M
disease IDO process
drug DRUGBANK Serine
drug DRUGBANK Trifluoro-thiamin phosphate
drug DRUGBANK Ilex paraguariensis leaf
disease IDO susceptibility
disease MESH Healthcare associated infection
drug DRUGBANK Meticillin
disease IDO site
drug DRUGBANK Methionine
drug DRUGBANK Ranitidine
disease MESH respiratory diseases
disease MESH emergency
disease IDO history
drug DRUGBANK Trestolone
disease IDO blood
drug DRUGBANK Clarithromycin
disease MESH allergies
drug DRUGBANK Aspartame
disease MESH COVID 19

Original Article

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