TY - JOUR
T1 - Estimation of caffeine regimens
T2 - A machine learning approach for enhanced clinical decision making at a neonatal intensive care unit (NICU)
AU - Shirwaikar, Rudresh Deepak
AU - Dinesh Acharya, U.
AU - Makkithaya, Krishnamoorthi
AU - Mallayaswamy, Surulivelrajan
AU - Lewis, Leslie Edward Simon
PY - 2018/1/1
Y1 - 2018/1/1
N2 - The decision-making process for estimating the optimal dosage is critical in clinical settings. In the neonatal intensive care unit (NICU), preterm neonates suffering from apnea of prematurity, optimum drug dosage can make a difference between life and death. To improve clinical decision making in the NICU, we have developed prediction models using machine learning algorithms. We have used optimized Support Vector Machine (SVM), decision trees with ensembles created using Bagging, Boosting, Random Forest, optimized Multi Layer Perceptron (MLP) and Deep Learning to predict adequacy of caffeine, a methylxanthine used to prevent the development of recurrent apneas, to reduce the need for mechanical ventilation. The respective models developed were evaluated using 100 clinical caffeine cases collected from the Neonatal Intensive Care Unit (NICU) of Kasturba Medical College, Manipal. Our results indicate that a deep belief network (DBN) having an area under curve (AUC) of 0.91, followed by an optimized MLP with the Score for Neonatal Acute Physiology I (SNAP I) as an input feature, outperform other models for assessing the drug effectiveness. Furthermore, the optimized MLP followed by a DBN, with SNAP I as an input feature is a more accurate model for predicting the therapeutic concentration of caffeine. These results suggest that the proposed SNAP I (illness severity score) acts as a critical input variable to enhance the performance of the prediction model. The machine learning approach is very useful for building decision support systems in the NICU in general, and it provides specific solutions to optimize the administration of lifesaving drugs to neonates who are very sensitive to dosages. Using our method, physicians can assess the adequacy and efficacy of caffeine on the study population in a NICU before administering it to neonates.
AB - The decision-making process for estimating the optimal dosage is critical in clinical settings. In the neonatal intensive care unit (NICU), preterm neonates suffering from apnea of prematurity, optimum drug dosage can make a difference between life and death. To improve clinical decision making in the NICU, we have developed prediction models using machine learning algorithms. We have used optimized Support Vector Machine (SVM), decision trees with ensembles created using Bagging, Boosting, Random Forest, optimized Multi Layer Perceptron (MLP) and Deep Learning to predict adequacy of caffeine, a methylxanthine used to prevent the development of recurrent apneas, to reduce the need for mechanical ventilation. The respective models developed were evaluated using 100 clinical caffeine cases collected from the Neonatal Intensive Care Unit (NICU) of Kasturba Medical College, Manipal. Our results indicate that a deep belief network (DBN) having an area under curve (AUC) of 0.91, followed by an optimized MLP with the Score for Neonatal Acute Physiology I (SNAP I) as an input feature, outperform other models for assessing the drug effectiveness. Furthermore, the optimized MLP followed by a DBN, with SNAP I as an input feature is a more accurate model for predicting the therapeutic concentration of caffeine. These results suggest that the proposed SNAP I (illness severity score) acts as a critical input variable to enhance the performance of the prediction model. The machine learning approach is very useful for building decision support systems in the NICU in general, and it provides specific solutions to optimize the administration of lifesaving drugs to neonates who are very sensitive to dosages. Using our method, physicians can assess the adequacy and efficacy of caffeine on the study population in a NICU before administering it to neonates.
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U2 - 10.1615/CritRevBiomedEng.2018025933
DO - 10.1615/CritRevBiomedEng.2018025933
M3 - Article
AN - SCOPUS:85055329226
SN - 0278-940X
VL - 46
SP - 93
EP - 115
JO - Critical Reviews in Biomedical Engineering
JF - Critical Reviews in Biomedical Engineering
IS - 2
ER -