Evidence map›Paper›PMID 41005021›Full record

SynthesisSeminars in arthritis and rheumatism2025

Identification of idiopathic inflammatory myopathy research cohorts using international classification of disease (ICD) codes: A systematic review.

Astia Allenzara, Jill Stachowski, Emily P Jones, Amanda E Nelson, Galen Foulke

Abstract readSystematic Review
In one paragraph

Synthesis in Seminars in arthritis and rheumatism, 2025. 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. 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

5 authors.

Astia AllenzaraDivision of Rheumatology, Allergy and Immunology and Thurston Arthritis Research Center, University of North Carolina at Chapel Hill, Chapel Hill, NC USA. Electronic address: astia.allenzara@unchealth.unc.edu.
Jill StachowskiPenn State Health Milton S Hershey Medical Center, School of Medicine, Hershey, PA USA.
Emily P JonesHealth Sciences Library, University of North Carolina at Chapel Hill, NC USA.
Amanda E NelsonDivision of Rheumatology, Allergy and Immunology and Thurston Arthritis Research Center, University of North Carolina at Chapel Hill, Chapel Hill, NC USA.
Galen FoulkePenn State Health Milton S Hershey Medical Center, Hershey, PA USA; Penn State Health Milton S Hershey Medical Center, Department of Public Health Sciences, Hershey, PA USA.

Funding

UNC Core Center for Clinical ResearchP30AR072580 · NIAMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Amanda E Nelson · 2019 to 2026
$6.1M
Mentoring in Patient Oriented Research in OsteoarthritisK24AR081368 · NIAMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Amanda E Nelson · 2022 to 2026
$916k
NIAMS NIH HHS K24 AR081368NIAMS NIH HHS L30 AR084776NIAMS NIH HHS P30 AR072580
6 · The paper itself

Abstract

objectiveTo summarize studies validating International Classification of Disease (ICD) coding for idiopathic inflammatory myopathies (IIM) case identification, focusing on dermatomyositis (DM) and polymyositis (PM).

methodsPubMed, Scopus, Embase, and CINAHL search was performed with a medical librarian (Prospero #CRD4202452377). Inclusion criteria required: English language, use of ICD-9 and/or -10 coding to identify cases, and clear method for validating cases.

results3684 citations were screened by title/abstract resulting in 69 full-text publications reviewed with 11 articles meeting inclusion criteria. Of the included studies, 5 evaluated only ICD-9, 5 evaluated only ICD-10, and one study evaluated both. All but one study in the US were single center, while those in Europe (n = 4) and Canada (n = 1) were population based. Reference standards varied, including Bohan and Peter (n = 5), 2017 EULAR/ACR classification (n = 2), expert opinion (n = 3), enrollment in Rheumatology Quality Register (n = 1) and muscle biopsy (n = 1). Four studies had a positive predictive value (PPV) of 0.9 or higher; two of these studies used coding associated with inpatient admission, and another required at least 2 codes (710.3) 3 months apart. Multiple coding instances decreased the sensitivity but increased PPV.

conclusionsICD coding is a valuable tool for identifying cases in bioinformatic research. Only a few studies describe ICD code validation for IIM research cohort construction. The highest PPV's are reported for DM and PM with the use of multiple coding instances, or those instances associated with inpatient admission.

Indexed as

DermatomyositisInternational Classification of DiseasesMyositisHumansDermatomyositisIdiopathic inflammatory myopathiesInternational classification of diseasesValidation

Identifiers

PMID41005021
PMCPMC12547942

What OpenQuestion holds

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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.