Evidence map›Paper›PMID 42678523›Full record

ArticlePediatric radiology2026

Quantifying human variability in pediatric bone age assessment: a multi-institutional multi-reader study and benchmark for AI evaluation.

Jin Long, David B Larson, Hans H Thodberg, Peter Bavngaard Thrane, Michelle Phung, Cicero T Silva, Neil U Lall, Alex Towbin, Sanjay P Prabhu, Curtis P Langlotz and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Pediatric 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

11 authors.

Jin LongSchool of Medicine, Department of Pediatrics, Stanford University, 1701 Page Mill Road, Palo Alto, CA, 94304, United States. jinlong@stanford.edu.ORCID https://orcid.org/0000-0002-6225-727X
David B LarsonSchool of Medicine, Department of Radiology, Stanford University, Stanford, United States.
Hans H ThodbergFremtidsvej 1, Visiana, 2970 Hørsholm, Denmark.
Peter Bavngaard ThraneFremtidsvej 1, Visiana, 2970 Hørsholm, Denmark.
Michelle PhungSchool of Medicine, Department of Radiology, Stanford University, Stanford, United States.
Cicero T SilvaSchool of Medicine, Department of Radiology and Biomedical Imaging, Yale University, New Haven, United States.
Neil U LallDepartment of Radiology, Children's Healthcare of Atlanta, Emory University School of Medicine, Atlanta, United States.
Alex TowbinDepartment of Radiology, Cincinnati Children's Hospital, University of Cincinnati College of Medicine, Cincinnati, United States.ORCID https://orcid.org/0000-0003-1729-5071
Sanjay P PrabhuDepartment of Radiology, Boston Children's Hospital, Harvard Medical School, Boston, United States.
Curtis P LanglotzSchool of Medicine, Department of Radiology, Stanford University, Stanford, United States.ORCID https://orcid.org/0000-0002-8972-8051
Sergios GatidisSchool of Medicine, Department of Radiology, Stanford University, Stanford, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBone age assessment using the Greulich and Pyle atlas is widely used in pediatrics but is subject to substantial reader variability. As artificial intelligence (AI) systems increasingly support clinical workflows, understanding the magnitude and structure of human variability is essential for contextualizing AI performance.

objectiveTo quantify human variability in pediatric bone age assessment across multiple institutions and to compare human variability with two automated bone age estimation methods. MATERIALS AND

methodsIn this multi-reader, multi-case study, 1,285 left-hand and wrist radiographs from five US academic centers were independently interpreted by four radiologists per case from a centrally administered pool of 22 radiologists recruited across nine institutions. Bone age estimates were obtained using the Greulich and Pyle atlas. Variability was assessed at the image, rater, and institution levels using mixed-effects modeling. Inter-reader variability was estimated while accounting for patient age and sex. Performance of two automated methods (BoneXpert and a deep-learning algorithm) was evaluated in an interchangeability analysis using a three-rater consensus reference. Accuracy metrics included mean absolute error (MAE), root mean square error (RMSE), and rates of substantial deviation (>1.8 years).

resultsWithin-image variability among radiologists was higher in younger patients (<12 years) than in older patients (standard deviation (SD) 8.7 months vs. 4.2 months, P<0.001). Between-institution variability decreased substantially after adjustment for patient age (8.9 months to 0.3 months). Inter-rater variability remained stable after adjustment (1.2 months). Variability was greater in male patients and younger age groups. Several radiologists demonstrated systematic biases related to age or sex. In comparison with individual human readers, BoneXpert showed lower error (MAE 4.8 months vs. 6.5 months) and variability, while the deep-learning algorithm performed similarly to human readers (MAE 6.3 months). Substantial deviations occurred in 0.7% of BoneXpert estimates, 2.4% of deep-learning estimates, and 3.4% of single human readings.

conclusionPediatric bone age assessment using the Greulich and Pyle method demonstrates measurable human reader variability, particularly in younger children and male patients. Automated methods performed within or beyond the observed range of human variability. These findings provide a quantitative benchmark for interpreting AI performance in skeletal maturity assessment.

Indexed as

Artificial intelligenceBone ageChildMachine learningObserver variationRadiographyReproducibility of results

Identifiers

What OpenQuestion holds

Textmetadata
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.