Development of a Risk Prediction Model for Arteriovenous Fistula Restenosis Following Percutaneous Transluminal Angioplasty in Maintenance Hemodialysis Patients Using SMOTE Algorithm
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引用次数: 0
Abstract
Background
Arteriovenous fistula (AVF) restenosis after percutaneous transluminal angioplasty (PTA) affects hemodialysis in maintenance hemodialysis (MHD) patients. Data imbalance limits predictive model accuracy.
Objective
To identify risk factors and develop a SMOTE-based risk prediction model for AVF restenosis within 12 months after PTA.
Methods
This retrospective cohort study enrolled 241 consecutive MHD patients with AVF stenosis undergoing PTA between July 2022 and July 2025. Each patient contributed one index PTA. Patients were divided into restenosis (45 cases) and nonrestenosis (196 cases) groups according to whether AVF restenosis occurred within 12 months after PTA. Univariate and multivariate logistic regression identified risk factors. The SMOTE algorithm addressed data imbalance. Model performance was evaluated by ROC curves, calibration curves, and decision curve analysis (DCA).
Results
Original-data multivariate analysis identified multisegmental stenosis, cannulation method, platelet count, and C-reactive protein (CRP) as independent risk factors. After SMOTE, intradialytic hypotension and serum albumin also became significant; however, these variables should be interpreted as exploratory because SMOTE does not create additional independent clinical information. The SMOTE-based model (P2) achieved AUC of 0.934 (training set) and 0.868 (validation set), outperforming the original model (P1).
Conclusion
The SMOTE-based model may help predict AVF restenosis within 12 months after PTA, but it is an exploratory internally validated tool and requires external validation before clinical use.
期刊介绍:
Cardiovascular Therapeutics (formerly Cardiovascular Drug Reviews) is a peer-reviewed, Open Access journal that publishes original research and review articles focusing on cardiovascular and clinical pharmacology, as well as clinical trials of new cardiovascular therapies. Articles on translational research, pharmacogenomics and personalized medicine, device, gene and cell therapies, and pharmacoepidemiology are also encouraged.
Subject areas include (but are by no means limited to):
Acute coronary syndrome
Arrhythmias
Atherosclerosis
Basic cardiac electrophysiology
Cardiac catheterization
Cardiac remodeling
Coagulation and thrombosis
Diabetic cardiovascular disease
Heart failure (systolic HF, HFrEF, diastolic HF, HFpEF)
Hyperlipidemia
Hypertension
Ischemic heart disease
Vascular biology
Ventricular assist devices
Molecular cardio-biology
Myocardial regeneration
Lipoprotein metabolism
Radial artery access
Percutaneous coronary intervention
Transcatheter aortic and mitral valve replacement.