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Updated: Aug 8, 2026

A Preterm Rat Model for Pain Studies
Published on: February 9, 2024
Biobehavioural reactivity to pain in preterm infants: a marker of neuromotor development
Ruth E Grunau1, Michael F Whitfield, Taryn Fay
1Centre for Community Child Health Research, Child and Family Research Institute, Canada. rgunau@cw.bc.ca
Insights
Neonatal pain reactivity during intensive care may predict infant motor development. Low pain response in preterm infants at 32 weeks postconceptional age correlated with poorer motor skills at 8 months corrected age.
Area of Science:
- Neonatology
- Developmental Pediatrics
- Neuroscience
Background:
- High-risk preterm infants experience significant stress during neonatal intensive care.
- Understanding early markers for neuromotor development is crucial for timely interventions.
Purpose of the Study:
- To investigate if pain reactivity in preterm infants predicts later neuromotor development.
- To assess the association between neonatal pain response and motor outcomes at 4 and 8 months corrected chronological age (CCA).
Main Methods:
- Studied 35 high-risk preterm infants (
- Measured behavioral and cardiac pain reactivity during heel lance at 32 weeks postconceptional age (PCA).
- Assessed neuromotor development using the Movement Assessment of Infants and Bayley Scales of Infant Development at 4 and 8 months CCA.
Main Results:
- Low biobehavioral pain reactivity at 32 weeks PCA was linked to poorer motor function quality at 8 months CCA.
- This association was not observed at 4 months CCA.
- Neonatal pain response showed potential as a predictive marker.
Conclusions:
- Pain reactivity before neonatal intensive care unit discharge may indicate future neuromotor development.
- Early pain response could serve as a valuable prognostic indicator for preterm infants.
Abstract:
In this preliminary study, it was examined whether capacity to react to external stress (acute pain) during neonatal intensive care predicts later neuromotor development at 4 and 8 months corrected chronological age (CCA) in high-risk preterm infants. Behavioural and cardiac reactivity to blood collection at 32 weeks postconceptional age (PCA) were recorded in addition to developmental outcomes at 4 and 8 months CCA in 35 preterm infants (17 males, 18 females) born

