Automated detection of abnormal general movements from pressure and positional information in hospitalized infants

Nathalie L Maitre1, Caitlin P Kjeldsen2, Andrea F Duncan3

  • 1Department of Pediatrics, Emory University School of Medicine and Children's Healthcare of Atlanta, Atlanta, GA, USA. nmaitre@emory.edu.

Pediatric Research
|July 30, 2024
PubMed

Insights

Automated detection of abnormal (cramped synchronized, or CS) general movements assessment (GMA) in infants shows promise for early identification of neuromotor disorders. This machine learning approach may increase access to GMA screening for at-risk newborns.

Area of Science:

  • Neonatal neurology
  • Developmental pediatrics
  • Computational neuroscience

Background:

  • Prechtl's general movements assessment (GMA) identifies abnormal (cramped synchronized, or CS) movement patterns with high sensitivity for predicting neuromotor disorders.
  • Clinical adoption of GMA is limited by training needs and subjective interpretation.

Purpose of the Study:

  • To develop and validate a preliminary, automated approach for detecting CS movements in infants using machine learning.
  • To create a clinically applicable software interface for automated GMA analysis.

Main Methods:

  • A three-phased approach combining unsupervised and supervised machine learning.
  • Dual data collection using video and a pressure-sensor mat from 335 hospitalized infants.
  • Feature extraction from clinician- and mat-derived data, followed by classification modeling.

Main Results:

  • A classification model integrating normalization, clustering, and decision tree methods achieved 100% sensitivity for CS movements.
  • Automated results were available within 20 minutes of data recording via a software interface.

Conclusions:

  • A feasible preliminary method for automated detection of abnormal GMA in neonates was developed by combining clinical research, machine learning, and sensor mat technology.
  • Further software and algorithm refinement is necessary for widespread clinical use.
Abstract