Evidence map›Paper›PMID 38366046›Full record

ArticleInsights into imaging2024

How AI should be used in radiology: assessing ambiguity and completeness of intended use statements of commercial AI products.

Kicky G van Leeuwen, Dennis M Hedderich, Hugh Harvey, Steven Schalekamp

Abstract read
In one paragraph

Article in Insights into imaging, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. 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

4 authors.

Kicky G van LeeuwenDepartment of Medical Imaging, Radboudumc, P.O. Box 9101, Nijmegen, 6500 HB, The Netherlands.
Dennis M HedderichSchool of Medicine, Department of Diagnostic and Interventional Neuroradiology, Klinikum Rechts Der Isar, Technical University of Munich, Munich, Germany.
Hugh HarveyHardian Health, Haywards Heath, UK.
Steven SchalekampDepartment of Medical Imaging, Radboudumc, P.O. Box 9101, Nijmegen, 6500 HB, The Netherlands. steven.schalekamp@radboudumc.nl.ORCID http://orcid.org/0000-0002-3984-3596

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIntended use statements (IUSs) are mandatory to obtain regulatory clearance for artificial intelligence (AI)-based medical devices in the European Union. In order to guide the safe use of AI-based medical devices, IUSs need to contain comprehensive and understandable information. This study analyzes the IUSs of CE-marked AI products listed on AIforRadiology.com for ambiguity and completeness.

methodsWe retrieved 157 IUSs of CE-marked AI products listed on AIforRadiology.com in September 2022. Duplicate products (n = 1), discontinued products (n = 3), and duplicate statements (n = 14) were excluded. The resulting IUSs were assessed for the presence of 6 items: medical indication, part of the body, patient population, user profile, use environment, and operating principle. Disclaimers, defined as contra-indications or warnings in the IUS, were identified and compared with claims.

resultsOf 139 AI products, the majority (n = 78) of IUSs mentioned 3 or less items. IUSs of only 7 products mentioned all 6 items. The intended body part (n = 115) and the operating principle (n = 116) were the most frequently mentioned components, while the intended use environment (n = 24) and intended patient population (n = 29) were mentioned less frequently. Fifty-six statements contained disclaimers that conflicted with the claims in 13 cases.

conclusionThe majority of IUSs of CE-marked AI-based medical devices lack substantial information and, in few cases, contradict the claims of the product. CRITICAL RELEVANCE STATEMENT: To ensure correct usage and to avoid off-label use or foreseeable misuse of AI-based medical devices in radiology, manufacturers are encouraged to provide more comprehensive and less ambiguous intended use statements. KEY POINTS: • Radiologists must know AI products' intended use to avoid off-label use or misuse. • Ninety-five percent (n = 132/139) of the intended use statements analyzed were incomplete. • Nine percent (n = 13) of the intended use statements held disclaimers contradicting the claim of the AI product. • Manufacturers and regulatory bodies must ensure that intended use statements are comprehensive.

Indexed as

Artificial intelligenceDevice approval processMedical device legislationMedical device safetyRadiology

Identifiers

PMID38366046
PMCPMC10873256

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.