# Machine learning-based prediction of 30-day unplanned readmission risk in day surgery lung cancer patients after lobectomy or sublobectomy: a real-world study

**Authors:** Nafei Han, Chuanbo An, Huadi Yuan, Meijuan Lan, Xiaoyan Wu, Li Liu, Xiaowei Yu, Xiajuan Jiang, Liyan Gao, Jing Fang

PMC · DOI: 10.3389/fmed.2026.1771501 · Frontiers in Medicine · 2026-02-20

## TL;DR

This study developed a machine learning model to predict 30-day unplanned readmissions after lung cancer surgery in day surgery patients, showing strong performance and identifying key risk factors.

## Contribution

The study introduces a high-performing random forest model for predicting readmission risk in day surgery lung cancer patients, validated in a real-world setting.

## Key findings

- The random forest model achieved a ROC-AUC of 0.939 and accuracy of 0.825 in predicting readmission risk.
- Key predictors included white-blood-cell count, prothrombin time, and intraoperative blood loss.
- The model showed favorable net benefit across a wide range of threshold probabilities and was well-calibrated.

## Abstract

Unplanned readmission within 30 days after lobectomy or sublobectomy for early stage lung cancer adversely affects patient recovery and healthcare costs. While machine-learning (ML) approaches offer potential for improved prediction, few models have been developed for day-surgery settings. This study aimed to develop and validate an ML-based model to predict 30-day unplanned readmission in lung cancer patients undergoing ambulatory lung resection.

We included patients who underwent lobectomy or sublobectomy in a day-surgery pathway between December 2022 and January 2025. The least absolute shrinkage and selection operator (LASSO) was used for feature selection. Data were split into training (70%) and validation (30%) sets. Nine ML algorithms were trained and evaluated using area under the receiver-operating-characteristic curve (ROC-AUC), precision-recall AUC (PR-AUC), accuracy, decision-curve analysis (DCA), and calibration curves. Model interpretability was assessed with SHapley Additive exPlanations (SHAP).

After propensity-score matching, 380 patients were analyzed, including 111 with unplanned readmission. LASSO identified 12 predictive features: age, payment category, prothrombin time (PT), white-blood-cell count (WBC), hemoglobin, intraoperative blood loss, surgical approach, pathological diagnosis, tumor count, tumor size, occupational category, and forced expiratory volume in 1 s (FEV1). The random forest (RF) model performed best in the validation set (ROC-AUC = 0.939, accuracy = 0.825), showed favorable net benefit across threshold probabilities of 10–80%, and was well-calibrated. SHAP analysis indicated WBC, PT, hemoglobin, intraoperative blood loss, and “unknown” occupational category as the top five predictors; WBC, PT, and blood loss were positively associated with readmission risk.

An RF-based model effectively predicted 30-day unplanned readmission after lung-cancer day surgery. The identified risk factors provide a basis for early stratification and targeted intervention, supporting optimized perioperative care in ambulatory settings.

## Linked entities

- **Diseases:** lung cancer (MONDO:0005138)

## Full-text entities

- **Genes:** SHROOM4 (shroom family member 4) [NCBI Gene 57477] {aka MRXSSDS, SHAP, shrm4}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** PT (MESH:D007020), impaired lung function (MESH:D003072), peripheral artery disease (MESH:D058729), postoperative (MESH:D019106), liver dysfunction (MESH:D017093), infection (MESH:D007239), hypovolemia (MESH:D020896), blood (MESH:D006402), died (MESH:D003643), shoulder arthroplasty (MESH:D000070599), squamous cell carcinoma (MESH:D002294), bleeding (MESH:D006470), mental illness (MESH:D001523), Lung cancer (MESH:D008175), cancer (MESH:D009369), adenocarcinoma (MESH:D000230), cardiopulmonary complications (MESH:D006323), blood loss (MESH:D016063), trauma (MESH:D014947), inflammatory (MESH:D007249)
- **Chemicals:** alcohol (MESH:D000438), carbon monoxide (MESH:D002248), oxygen (MESH:D010100)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12963241/full.md

## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12963241/full.md

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Source: https://tomesphere.com/paper/PMC12963241