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Published on: May 2, 2012
Development and validation of a risk prediction model for multidrug-resistant organisms infection in diabetic foot
Jinghang Zhang1, Xuemei Li1, Bai Chang1
1NHC Key Lab of Hormones and Development and Tianjin Key Lab of Metabolic Diseases, Tianjin Medical University Chu Hsien-I Memorial Hospital & Institute of Endocrinology, Tianjin, China.
Objective:
To develop and validate a nomogram for predicting the risk of multidrug-resistant organisms (MDROs) infection in diabetic foot ulcer (DFU) patients.
Methods:
701 DFU patients were divided into training (491 cases) and validation (210 cases) sets (7:3 ratio). Multivariate logistic regression analysis was performed to identify the independent risk factors for MDRO infection in DFU patients. Two nomogram prediction models were developed based on the independent risk factors. The predictive efficacy of the prediction models was evaluated using the receiver operating characteristic (ROC) curve and calibration curve analysis. The decision curve analysis (DCA) was performed to evaluate the prediction model's performance during clinical application.
Results:
Multivariate logistic regression analysis identified previous antibiotic therapy, surgical therapy, ulcer size>4cm2, and CRP as independent risk factors. Two models were developed and validated based on the analysis. Model 1 included previous antibiotic therapy, surgical therapy, and ulcer size>4cm2. Model 2 added a further laboratory indicator to Model 1, such as CRP. In the training set, the AUC of the nomogram for Model 1and Model 2 was 0.763(95% CI 0.711-0.815) and 0.789 (95% CI 0.740-0.838), respectively, and 0.837 (95% CI 0.744-0.900) and 0.845 (95% CI 0.785-0.905) in the validation set. The Youden indexes for Models 1and 2 were 0.416 and 0.470 in the training set and 0.558 and 0.588 in the validation set, respectively. Notably, Model 2 showed higher sensitivity and specificity. The calibration plot and Hosmer-Lemeshow test for Model 1 and Model 2 indicated that the predicted probability had good consistency with the actual probability in both the training set (P = 0.689 for Model 1 and P = 0.139 for Model 2) and validation set (P = 0.607 for Model 1and P = 0.635 for Model 2). The DCA curve indicated that the models had good clinical utility. All models performed well for both discrimination and calibration.
Conclusion:
This study developed two nomogram models for predicting MDRO infection risk in DFU patients. Model 2, with superior predictive performance, enables early identification of high-risk patients. These models facilitate targeted interventions, potentially reducing MDRO complications and healthcare burdens.
Insights
This study developed nomogram models to predict multidrug-resistant organism (MDRO) infection risk in diabetic foot ulcer (DFU) patients. Model 2 demonstrated superior performance, aiding early identification and targeted interventions for high-risk individuals.
Area of Science:
- Infectious Diseases
- Diabetology
- Medical Informatics
Background:
- Diabetic foot ulcers (DFUs) are prone to infections, including those caused by multidrug-resistant organisms (MDROs).
- Accurate risk prediction for MDRO infections in DFU patients is crucial for effective management and prevention of complications.
Purpose of the Study:
- To develop and validate nomogram models for predicting the risk of MDRO infection in patients with diabetic foot ulcers.
- To identify independent risk factors associated with MDRO infections in this patient population.
Main Methods:
- A cohort of 701 DFU patients was divided into training (491) and validation (210) sets.
- Multivariate logistic regression was used to identify independent risk factors.
- Two nomogram models were constructed and validated using ROC curve, calibration curve, and decision curve analysis.
Main Results:
- Previous antibiotic therapy, surgical therapy, ulcer size > 4cm², and CRP were identified as independent risk factors.
- Both developed nomogram models demonstrated good predictive performance, with Model 2 (including CRP) showing slightly superior accuracy (AUCs ranging from 0.763 to 0.845).
- Calibration plots and decision curve analysis confirmed the models' good consistency and clinical utility.
Conclusions:
- Two validated nomogram models can predict MDRO infection risk in DFU patients.
- Model 2 offers enhanced predictive performance, facilitating early identification of high-risk patients.
- These models support targeted interventions, potentially reducing MDRO complications and healthcare costs.
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