Evidence map›Paper›PMID 38737141›Full record

ArticleJAMIA open2024

Phenotype execution and modeling architecture to support disease surveillance and real-world evidence studies: English sentinel network evaluation.

Gavin Jamie, William Elson, Debasish Kar, Rashmi Wimalaratna, Uy Hoang, Bernardo Meza-Torres, Anna Forbes, William Hinton, Sneha Anand, Filipa Ferreira and 4 more

Abstract read
In one paragraph

Article in JAMIA open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Validation of an acute respiratory infection phenotyping algorithm to support robust computerised medical record-based respiratory sentinel surveillance, England, 2023.Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin · 2024
    Article
  3. 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

14 authors.

Gavin JamieNuffield Department of Primary Health Care Sciences, University of Oxford, Oxford, OX2 6ED, United Kingdom.ORCID https://orcid.org/0000-0001-9147-7784
William ElsonNuffield Department of Primary Health Care Sciences, University of Oxford, Oxford, OX2 6ED, United Kingdom.
Debasish KarNuffield Department of Primary Health Care Sciences, University of Oxford, Oxford, OX2 6ED, United Kingdom.
Rashmi WimalaratnaNuffield Department of Primary Health Care Sciences, University of Oxford, Oxford, OX2 6ED, United Kingdom.
Uy HoangNuffield Department of Primary Health Care Sciences, University of Oxford, Oxford, OX2 6ED, United Kingdom.ORCID https://orcid.org/0000-0002-8428-5140
Bernardo Meza-TorresNuffield Department of Primary Health Care Sciences, University of Oxford, Oxford, OX2 6ED, United Kingdom.
Anna ForbesNuffield Department of Primary Health Care Sciences, University of Oxford, Oxford, OX2 6ED, United Kingdom.
William HintonNuffield Department of Primary Health Care Sciences, University of Oxford, Oxford, OX2 6ED, United Kingdom.
Sneha AnandNuffield Department of Primary Health Care Sciences, University of Oxford, Oxford, OX2 6ED, United Kingdom.ORCID https://orcid.org/0000-0002-0538-3974
Filipa FerreiraNuffield Department of Primary Health Care Sciences, University of Oxford, Oxford, OX2 6ED, United Kingdom.ORCID https://orcid.org/0000-0003-0083-4809
Rachel ByfordNuffield Department of Primary Health Care Sciences, University of Oxford, Oxford, OX2 6ED, United Kingdom.ORCID https://orcid.org/0000-0002-4792-8995
Jose Ordonez-MenaNuffield Department of Primary Health Care Sciences, University of Oxford, Oxford, OX2 6ED, United Kingdom.
Utkarsh AgrawalNuffield Department of Primary Health Care Sciences, University of Oxford, Oxford, OX2 6ED, United Kingdom.ORCID https://orcid.org/0000-0002-3889-544X
Simon de LusignanNuffield Department of Primary Health Care Sciences, University of Oxford, Oxford, OX2 6ED, United Kingdom.ORCID https://orcid.org/0000-0002-8553-2641

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To evaluate Phenotype Execution and Modelling Architecture (PhEMA), to express sharable phenotypes using Clinical Quality Language (CQL) and intensional Systematised Nomenclature of Medicine (SNOMED) Clinical Terms (CT) Fast Healthcare Interoperability Resources (FHIR) valuesets, for exemplar chronic disease, sociodemographic risk factor, and surveillance phenotypes. Method: We curated 3 phenotypes: Type 2 diabetes mellitus (T2DM), excessive alcohol use, and incident influenza-like illness (ILI) using CQL to define clinical and administrative logic. We defined our phenotypes with valuesets, using SNOMED's hierarchy and expression constraint language, and CQL, combining valuesets and adding temporal elements where needed. We compared the count of cases found using PhEMA with our existing approach using convenience datasets. We assessed our new approach against published desiderata for phenotypes. Results: The T2DM phenotype could be defined as 2 intensionally defined SNOMED valuesets and a CQL script. It increased the prevalence from 7.2% to 7.3%. Excess alcohol phenotype was defined by valuesets that added qualitative clinical terms to the quantitative conceptual definitions we currently use; this change increased prevalence by 58%, from 1.2% to 1.9%. We created an ILI valueset with SNOMED concepts, adding a temporal element using CQL to differentiate new episodes. This increased the weekly incidence in our convenience sample (weeks 26-38) from 0.95 cases to 1.11 cases per 100 000 people. Conclusions: Phenotypes for surveillance and research can be described fully and comprehensibly using CQL and intensional FHIR valuesets. Our use case phenotypes identified a greater number of cases, whilst anticipated from excessive alcohol this was not for our other variable. This may have been due to our use of SNOMED CT hierarchy. Our new process fulfilled a greater number of phenotype desiderata than the one that we had used previously, mostly in the modeling domain. More work is needed to implement that sharing and warehousing domains.

Indexed as

clinical codingcomputerizedmedical record systemsphenotyperoutinely collected health datasystematized nomenclature of medicine

Identifiers

PMID38737141
PMCPMC11087727

What OpenQuestion holds

Textmetadata
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.