Evidence map›Paper›PMID 40413381›Full record

ArticleBMC medical research methodology2025

An automation framework for clinical codelist development validated with UK data from patients with multiple long-term conditions.

A Aslam, L Walker, M Abaho, H Cant, M O'Connell, A S Abuzour, L Hama, P Schofield, F S Mair, R A Ruddle and 9 more

Abstract read
In one paragraph

Article in BMC medical research methodology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

19 authors.

A AslamInformation School, University of Sheffield, Sheffield, UK. a.aslam@sheffield.ac.uk.
L WalkerWolfson Centre for Personalised Medicine, University of Liverpool, Liverpool, UK.
M AbahoWolfson Centre for Personalised Medicine, University of Liverpool, Liverpool, UK.
H CantDivision of Informatics, Imaging & Data Science, University of Manchester, Manchester, UK.
M O'ConnellDivision of Informatics, Imaging & Data Science, University of Manchester, Manchester, UK.
A S AbuzourInstitute of Health Sciences, Faculty of Medicine & Health, University of Leeds, Leeds, UK.
L HamaSchool of Computing, University of Leeds, Leeds, UK.
P SchofieldWolfson Centre for Personalised Medicine, University of Liverpool, Liverpool, UK.
F S MairGeneral Practice and Primary Care, School of Health and Wellbeing, University of Glasgow, Glasgow, UK.
R A RuddleSchool of Computing, University of Leeds, Leeds, UK.
O PopoolaMerseycare NHS Foundation Trust, Liverpool, UK.
M SperrinDivision of Informatics, Imaging & Data Science, University of Manchester, Manchester, UK.
J Y TsangDivision of Population Health, University of Manchester, Manchester, UK.
E ShantsilaDepartment of Primary Care and Mental Health, University of Liverpool, Liverpool, UK.
M GabbayInstitute of Population Health, Faculty of Health and Life Sciences, University of Liverpool, Liverpool, UK.
A CleggInstitute of Health Sciences, Faculty of Medicine & Health, University of Leeds, Leeds, UK.
A A WoodallWolfson Centre for Personalised Medicine, University of Liverpool, Liverpool, UK.
I BuchanWolfson Centre for Personalised Medicine, University of Liverpool, Liverpool, UK.
S D ReltonInstitute of Health Sciences, Faculty of Medicine & Health, University of Leeds, Leeds, UK.

Funding

National Institute for Health and Care Research (NIHR)
6 · The paper itself

Abstract

backgroundCodelists play a crucial role in ensuring accurate and standardized communication within healthcare. However, preparation of high-quality codelists is a rigorous and time-consuming process. The literature focuses on transparency of clinical codelists and overlooks the utility of automation. METHODS (AUTOMATED FRAMEWORK DESIGN AND USE-CASE: DYNAIRX): Here we present a Codelist Generation Framework that can automate generation of codelists with minimal input from clinical experts. We demonstrate the process using a specific project, DynAIRx, producing appropriate codelists and a framework allowing future projects to take advantage of automated codelist generation. Both the framework and codelist are publicly available. DynAIRx is an NIHR-funded project aiming to develop AIs to help optimise prescribing of medicines in patients with multiple long-term conditions. DynAIRx requires complex codelists to describe the trajectory of each patient, and the interaction between their conditions. We promptly generated

resultsThe framework reduced the clinician time required to validate codes, automatically shrunk codelists using trusted sources and added new codes for review against existing codelists. In the DynAIRx case study, a codelist of

conclusionThis work examines current methodologies for codelist development and the challenges associated with ensuring transparency and reproducibility. A key benefit of this approach is its emphasis on automation and reliance on trusted sources, which significantly lowers the workload, minimizes human error, and saves substantial time, particularly the time needed from clinical experts.

Indexed as

AutomationClinical CodingHumansReproducibility of ResultsUnited KingdomAutomationCodelistDynAIRxMultiple long term conditions (MLTC)SNOMEDs

Identifiers

PMID40413381
PMCPMC12102889

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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.