Evidence map›Paper›PMID 42286177›Full record

ArticleEuropean radiology2026

The current state of demographic subgroup reporting for commercially available AI for radiology: a scoping review.

Shannon L Walston, Hirotaka Takita, Yasuhito Mitsuyama, Junya Sato, Daiju Ueda

Abstract readScoping Review
In one paragraph

Article in European radiology, 2026. 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

5 authors.

Shannon L WalstonDepartment of Artificial Intelligence, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan. shannongross3@gmail.com.ORCID http://orcid.org/0000-0002-7268-8313
Hirotaka TakitaDepartment of Diagnostic and Interventional Radiology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
Yasuhito MitsuyamaDepartment of Diagnostic and Interventional Radiology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
Junya SatoDepartment of Artificial Intelligence in Diagnostic Radiology, The University of Osaka, Graduate School of Medicine, Suita, Japan.
Daiju UedaDepartment of Artificial Intelligence, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan. ai.labo.ocu@gmail.com.

Funding

Japan Science and Technology Agency JPMJPR2521
6 · The paper itself

Abstract

objectiveThough subgroup performance reporting helps ensure the safety of artificial intelligence (AI) products, the extent of this reporting remains unclear. This scoping review identifies studies validating commercially available AI-based products and reports the trends in performance reporting across sex, age, and race/ethnicity demographic subgroups. MATERIALS AND

methodsPeer-reviewed validation studies of commercially available products published after 2010 were collected from the Health AI Register and PubMed on 29 November 2024. Study trends in the reporting of sex, age, and race/ethnicity were mapped with regression analysis. We apply the Wilson confidence interval equation to estimate which tuberculosis detection studies are underpowered for subgroup meta-analysis.

resultsThree hundred ninety-two of 545 studies validating 252 products reported subgroup demographic data for any of the three groups. Only 77 of these presented subgroup performance results. Skeletal (20/88) and lung (30/139) studies, and those utilizing chest (24/79) or bone (19/63) radiographs, most often presented subgroup performance data. We found no evidence that more recent studies (OR: 1.039 [95% CI: 0.959-1.127]) or company sponsorship (OR: 1.010 [95% CI: 0.492-1.920]) led to increased subgroup reporting. We show that 14/21 tuberculosis datasets may be underpowered for post-hoc subgroup meta-analysis.

conclusionThis scoping review quantifies how fragmented the commercial validation landscape is, showing that reporting for both the demographics and per-subgroup performance is inadequate for estimating subgroup bias. This systemic problem requires effort from all stakeholders, from researchers to regulatory agencies, encouraging thorough reporting and commercial product validation to support physician and patient trust in medical AI products. KEY POINTS: Question The number of studies validating the performance of each commercially available radiology AI product for minority subgroup bias is unclear. Findings The currently available commercial AI validation studies often neglect to describe demographic subgroup data, and fewer provide performance results per subgroup, prohibiting algorithmic bias meta-analysis. Clinical relevance Physician and patient trust in the medical AI already used clinically must be built on peer-reviewed literature and meta-analysis. The current literature is insufficient for determining the safety and performance of these products for demographic minorities.

Indexed as

Artificial IntelligenceRadiologyDemographyHumansArtificial intelligenceComputer-assistedOdds ratioRadiographic image interpretationRadiologySecondary data analysis

Identifiers

PMID42286177
PMCPMC13574847

What OpenQuestion holds

Textmetadata
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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.