Evidence map›Paper›PMID 36532317›Full record

ArticleRheumatology advances in practice2022

Validation of methods to identify people with idiopathic inflammatory myopathies using hospital episode statistics.

Jennifer R Hannah, Patrick A Gordon, James Galloway, Megan Rutter, Emily J Peach, Michael Rooney, Peter Stilwell, Matthew J Grainge, Peter C Lanyon, Mary Bythell and 1 more

Open access · goldAbstract read
In one paragraph

Article in Rheumatology advances in practice, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
1.9field-weighted citation impact, top 14% of its field
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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it, 14 citations in OpenAlex.

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  11. Digital Approaches for Myositis.Current rheumatology reports · 2023
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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 at 5 institutions in 1 country.

Jennifer R HannahCentre for Rheumatic Diseases, King's College London, London, UK.ORCID https://orcid.org/0000-0002-3491-6653
Patrick A GordonCentre for Rheumatic Diseases, King's College London, London, UK.
James GallowayCentre for Rheumatic Diseases, King's College London, London, UK.
Megan RutterNational Congenital Anomaly and Rare Disease Registration Service, NHS Digital, London, UK.
Emily J PeachLifespan and Population Health, University of Nottingham, Nottingham, UK.
Michael RooneyDepartment of Rheumatology, King's College Hospital, London, UK.
Peter StilwellNational Congenital Anomaly and Rare Disease Registration Service, NHS Digital, London, UK.
Matthew J GraingeLifespan and Population Health, University of Nottingham, Nottingham, UK.ORCID https://orcid.org/0000-0001-7181-4042
Peter C LanyonNational Congenital Anomaly and Rare Disease Registration Service, NHS Digital, London, UK.
Mary BythellNational Congenital Anomaly and Rare Disease Registration Service, NHS Digital, London, UK.
Fiona A PearceNational Congenital Anomaly and Rare Disease Registration Service, NHS Digital, London, UK.ORCID https://orcid.org/0000-0003-2884-1998
King's College London · GBNottingham University Hospitals NHS Trust · GBNHS Digital · GBUniversity of Nottingham · GBKing's College Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Hospital episode statistics (HES) are routinely recorded at every hospital admission within the National Health Service (NHS) in England. This study validates diagnostic ICD-10 codes within HES as a method of identifying cases of idiopathic inflammatory myopathies (IIMs). Methods: All inpatient admissions at one NHS Trust between 2010 and 2020 with relevant diagnostic ICD-10 codes were extracted from HES. Hospital databases were used to identify all outpatients with IIM, and electronic care records were reviewed to confirm coding accuracy. Total hospital admissions were calculated from NHS Digital reports. The sensitivity and specificity of each code and code combinations were calculated to develop an optimal algorithm. The optimal algorithm was tested in a sample of admissions at another NHS Trust. Results: Of the 672 individuals identified by HES, 510 were confirmed to have IIM. Overall, the positive predictive value (PPV) was 76% and sensitivity 89%. Combination algorithms achieved PPVs between 89 and 94%. HES can also predict the presence of IIM-associated interstitial lung disease (ILD) with a PPV of 79% and sensitivity of 71%. The optimal algorithm excluded children (except JDM code M33.0), combined M33.0, M33.1, M33.9, M36.0, G72.4, M60.8 and M33.2, and included M60.9 only if it occurred alongside an ILD code (J84.1, J84.9 or J99.1). This produced a PPV of 88.9% and sensitivity of 84.2%. Retesting this algorithm at another NHS Trust confirmed a high PPV (94.4%). Conclusion: IIM ICD-10 code combinations in HES have high PPVs and sensitivities. Algorithms tested in this study could be applied across all NHS Trusts to enable robust and cost-effective whole-population research into the epidemiology of IIM.

Indexed as

epidemiologyfindabilityhospital episode statisticsICD-10myositisrare diseases

Identifiers

PMID36532317
PMCPMC9749128
OpenAlexW4310558694

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.