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Updated: Jan 20, 2026

Measuring Pain-Evoked Brain Activity in Neonates Using a Flat-Tip Probe Coupled to EEG
Neonatal functional brain maturation in the context of perioperative critical care and pain management: A case report
Duncan Jack Hodkinson1,2, Chandler Rebecca Lee Mongerson1, Russell William Jennings2,3
1Department of Anesthesiology, Critical Care and Pain Medicine, Boston Children's Hospital, 300 Longwood Ave., Bader 3, Boston, MA.
Insights
Resting-state functional magnetic resonance imaging (rs-fMRI) is feasible in critically ill infants, revealing brain network changes after critical care. This pilot study highlights rs-fMRI
Area of Science:
- Neuroscience
- Pediatric Critical Care
- Medical Imaging
Background:
- The infant brain exhibits significant plasticity, making it vulnerable during early development.
- Resting-state functional magnetic resonance imaging (rs-fMRI) offers insights into neuroplasticity related to interventions or brain injuries.
- This pilot study aimed to assess the feasibility of rs-fMRI in infants within a pediatric perioperative critical care setting.
Observation:
- A case study involving a premature infant with esophageal atresia, who underwent complex perioperative care and presented with a subdural hematoma.
- Rs-fMRI scans were acquired before and after the critical care period (at 1-month and 2.25-months corrected age).
- Graph theory analysis was employed to evaluate resting-state functional connectivity (RSFC) and brain network complexity.
Findings:
- Head circumference transiently increased, coinciding with sedation changes, and met criteria for hydrocephalus but not macrocephaly.
- RSFC analysis revealed networks consistent with established literature.
- Qualitative differences in correlated and anticorrelated spontaneous brain activity were observed between pre- and post-treatment scans.
Implications:
- Current macrocephaly definitions may need adjustment for monitoring critically ill infants.
- The study demonstrates the successful application of rs-fMRI in a critically ill infant with brain pathology.
- Future research should focus on group-level RSFC studies to understand network homeostasis in both healthy and critically ill developing infants.
Introduction:
Remarkable plasticity during the first year of life imparts heighted vulnerability of the developing infant brain. Application of resting-state functional magnetic resonance imaging (rs-fMRI) in infants may contribute to our understanding of neuroplastic changes associated with therapeutic interventions and/or brain insults. In addition to showing clinically relevant incidental brain MRI findings, the objective of our pilot study was to test feasibility of rs-fMRI methods at this early age in the context of pediatric perioperative critical care.
Methods:
We report the case of a former 33-week premature infant born with long-gap esophageal atresia that underwent complex perioperative critical care (Foker process) requiring prolonged post-operative sedation and whom presented with incidental subdural hematoma. Rs-fMRI data was acquired before (at 1-month corrected age) and after (at 2.25-months corrected age) complex perioperative care. We evaluated resting-state functional connectivity (RSFC) using graph theory to explore the complex structure of brain networks.
Results:
A transient increase in head circumference coincided temporally with lifting of sedation and initiation of sedation drugs weaning, and qualified for hydrocephalus (93%) but not macrocephaly (>95%). RSFC analysis identified networks spatially consistent with those previously described in the literature, with notable pre-post-treatment qualitative differences in correlated and anticorrelated spontaneous brain activity.
Discussion:
Current definitions of macrocephaly may require lower threshold criteria for monitoring of critically ill infants. Although we demonstrate that available rs-fMRI could be effectively applied in a critically ill infant in the setting of brain pathology, future group-level studies should investigate RSFC to evaluate maintenance of network homeostasis during development of both healthy and critically ill infants.
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