Why the study?
Preterm infants are frequently exposed to severe cardio-respiratory events combining apnea, bradycardia, and oxygen desaturation, motivating a model-based approach to analyze acute heart rate responses.
A novel patient-specific computational model can accurately simulate heart rate responses to apnea in preterm infants, potentially aiding in personalized diagnosis and treatment.
May aid personalized analysis of neonatal apnea-bradycardia; leaves open validation before any clinical adoption.
OBJECTIVE: Preterm infants are particularly exposed to severe cardio-respiratory events, associating apnea with bradycardia and oxygen desaturation. A patient-specific and event-specific model-based approach is proposed in this work to analyze the acute heart rate response to apnea-bradycardia events in preterm newborn. METHODS: A novel model integrating the main cardio-respiratory interactions which are specific to the neonatal period is proposed. An evolutionary algorithm is applied to estimate patient-specific model parameters from a database of 37 apnea-bradycardia episodes acquired from 10 preterm newborns. Unsupervised clustering (K-means) was applied to the identified parameters to define phenogroups of cardio-respiratory responses to apnea. RESULTS: A significant correspondence was observed between simulated and experimental heart rate series in all identifications (median RMSE = 8.85 bpm). Three clusters of parameters were found and were associated to three different pathophysiological dynamics related to apnea-bradycardia. CONCLUSION AND SIGNIFICANCE: The proposed method, based on patient and event-specific model parameter identification, provides a novel approach to characterize bradycardia dynamics in response to apnea, opening the way to the proposal of new personalized diagnosis and treatment possibilities in this particularly sensitive population.
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Duport et al. (2024) studied this question.
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