Healthcare
Predicting proximal junctional failure in adult spinal deformity patients using machine learning models based on spinal alignment parameters
By Akihiko Hiyama, Daisuke Sakai, Hiroyuki Katoh, Masato Sato & Masahiko Watanabe • Scientific Reports • Published online: 20 November 2025
Executive Impact: AI in Spinal Deformity Prediction
This study evaluated five machine learning (ML) models (Random Forest, Logistic Regression, Support Vector Machine (SVM), Decision Tree, and Naive Bayes) to predict Proximal Junctional Failure (PJF) in Adult Spinal Deformity (ASD) patients after two-stage corrective surgery. Using preoperative and postoperative spinal alignment parameters, Random Forest achieved the highest mean accuracy (78.4%) and Area Under the Curve (AUC = 0.704). The predicted probabilities for PJF were significantly higher in the PJF group (0.306 ± 0.181) compared to non-PJF cases (0.186 ± 0.164, p = 0.0057). The model demonstrated robustness with cross-validation (fivefold: 79.4%, tenfold: 77.3%). The findings suggest Random Forest can be a reliable tool for early PJF risk stratification. Future work includes incorporating bone mineral density, comorbidities, and multicenter validation.
Deep Analysis & Enterprise Applications
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In the healthcare sector, AI can revolutionize diagnostics, treatment planning, and predictive analytics. This study demonstrates how machine learning, specifically Random Forest, can identify patients at high risk for Proximal Junctional Failure (PJF) after adult spinal deformity surgery. By leveraging spinal alignment parameters, AI models can support clinicians in making data-driven decisions, leading to personalized risk stratification and improved patient outcomes.
| Model | Mean Accuracy (%) | Key Strengths |
|---|---|---|
| Random Forest | 78.4 |
|
| SVM | 73.4 |
|
| Logistic Regression | 70.0 |
|
| Decision Tree | 67.2 |
|
| Naive Bayes | 64.0 |
|
Enterprise Process Flow
Random Forest in Clinical Decision Support
The Random Forest model demonstrated a higher net benefit compared to 'treat-all' and 'treat-none' strategies across clinically relevant threshold probabilities (0.10 to 0.40). This indicates its potential to guide interventions, identifying high-risk patients for enhanced postoperative surveillance and minimizing unnecessary treatment for low-risk individuals. The model's capacity to distinguish between PJF and non-PJF groups, with significantly higher predicted probabilities for the PJF group, underscores its clinical utility for personalized risk stratification.
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