Evidence map›Paper›PMID 42051705›Full record

ArticleFrontiers in medicine2026

An integrated clinical and imaging model for predicting post-traumatic nonunion.

Bin Wang, Kaipan Qu

Abstract read
In one paragraph

Article in Frontiers in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

2 authors.

Bin WangNavy 971st Hospital of PLA, Qingdao, China.
Kaipan QuDepartment of Trauma and Hand Foot Surgery, Shandong Provincial Third Hospital, Jinan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: This model aims to support early risk stratification and clinical decision-making. Methods: A retrospective cohort of 343 patients with unilateral closed long bone fractures treated by internal fixation was analyzed. Clinico-radiological variables-including Injury Severity Index, maximum fracture gap width, volume of cystic changes, callus volume growth rate, and Radiographic Union Scale for Tibial fractures (RUST) score-were systematically collected. Predictors were selected using Least Absolute Shrinkage and Selection Operator (LASSO) regression. Multivariable logistic regression and multiple machine learning algorithms (e.g., random forest, gradient boosting machine) were applied. The dataset was split 7:3 into training and validation sets. All feature selection and model hyperparameter tuning were restricted to the training set, information leakage was avoided via 10-fold cross-validation, and a single evaluation was finally conducted on the independent validation set. Model performance was assessed using the area under the receiver operating characteristic curve (AUC), calibration curves, and decision curve analysis. Results: Training and validation cohorts exhibited comparable baseline characteristics. Five independent predictors were identified: Injury Severity Index, maximum fracture gap width, and cystic change volume were risk factors, whereas callus growth rate and RUST score were protective. The gradient boosting machine model achieved the highest predictive accuracy, with an AUC of 0.866 (95% Confidence Interval (CI): 0.783-0.948) in training and 0.858 (95% CI: 0.716-1.000) in validation. Calibration was satisfactory, and decision curve analysis demonstrated a superior net benefit across threshold probabilities. A nomogram was constructed, and SHapley Additive exPlanations (SHAP) analysis improved interpretability. Conclusion: A machine learning model integrating clinical and imaging predictors was successfully developed and validated for predicting post-traumatic nonunion. It exhibits strong discriminative ability and may assist in personalized treatment planning.

Indexed as

imagemachine learningpost-traumatic nonunionprediction modelSHAP

Identifiers

PMID42051705
PMCPMC13111060

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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.