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Comparison of Multivariable Logistic Regression and Machine Learning Models for Predicting Bronchopulmonary Dysplasia
Faiza Khurshid1, Helen Coo1, Amal Khalil2
1Department of Pediatrics, Queen's University, Kingston, ON, Canada.
Insights
Machine learning models accurately predict bronchopulmonary dysplasia (BPD) or death in premature infants. These models offer improved risk assessment at multiple time points for diverse populations.
Area of Science:
- Neonatal Medicine
- Computational Biology
- Clinical Prediction Modeling
Background:
- Bronchopulmonary dysplasia (BPD) is a major complication of prematurity.
- Existing prediction models for BPD have limitations in timing and population diversity.
- Early identification of at-risk infants is crucial for timely intervention.
Purpose of the Study:
- To compare the performance of machine learning (ML) and logistic regression (LR) models in predicting BPD or death.
- To develop accurate and timely risk prediction models for premature infants.
- To create models suitable for ethno-diverse populations.
Main Methods:
- Utilized a cohort of infants <33 weeks' gestational age (GA) from the Canadian Neonatal Network (2016-2018).
- Developed prediction models for BPD/death at 1, 7, and 14 days post-admission using ML and LR algorithms.
- Employed 10-fold cross-validation and a 20% hold-out sample to evaluate model performance (AUC, calibration).
Main Results:
- Model AUCs ranged from 0.811 to 0.886, indicating strong predictive performance.
- Discrimination was lower in the <29 weeks' GA subcohort (AUCs 0.699-0.790).
- Some ML models demonstrated suboptimal calibration, necessitating further refinement.
Conclusions:
- ML and LR models show promise for predicting BPD/death in premature infants.
- Top-performing algorithms will inform the development of multinomial models and an online risk estimator.
- Future models aim to predict BPD severity and death without requiring ethnicity data.
Abstract:
Bronchopulmonary dysplasia (BPD) is the most prevalent and clinically significant complication of prematurity. Accurate identification of at-risk infants would enable ongoing intervention to improve outcomes. Although postnatal exposures are known to affect an infant's likelihood of developing BPD, most existing BPD prediction models do not allow risk to be evaluated at different time points, and/or are not suitable for use in ethno-diverse populations. A comprehensive approach to developing clinical prediction models avoids assumptions as to which method will yield the optimal results by testing multiple algorithms/models. We compared the performance of machine learning and logistic regression models in predicting BPD/death. Our main cohort included infants <33 weeks' gestational age (GA) admitted to a Canadian Neonatal Network site from 2016 to 2018 (n = 9,006) with all analyses repeated for the <29 weeks' GA subcohort (n = 4,246). Models were developed to predict, on days 1, 7, and 14 of admission to neonatal intensive care, the composite outcome of BPD/death prior to discharge. Ten-fold cross-validation and a 20% hold-out sample were used to measure area under the curve (AUC). Calibration intercepts and slopes were estimated by regressing the outcome on the log-odds of the predicted probabilities. The model AUCs ranged from 0.811 to 0.886. Model discrimination was lower in the <29 weeks' GA subcohort (AUCs 0.699-0.790). Several machine learning models had a suboptimal calibration intercept and/or slope (k-nearest neighbor, random forest, artificial neural network, stacking neural network ensemble). The top-performing algorithms will be used to develop multinomial models and an online risk estimator for predicting BPD severity and death that does not require information on ethnicity.
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