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Electrophysiological Measurements and Analysis of Nociception in Human Infants
Published on: December 20, 2011
Cortical pain responses in human infants
Rebeccah Slater1, Anne Cantarella, Shiromi Gallella
1The London Pain Consortium, Department of Anatomy and Developmental Biology, University College London, London WC1E 6BT, United Kingdom. r.slater@ucl.ac.uk
Insights
Premature infants as young as 25 weeks can process pain at a cortical level, as shown by brain activity changes during noxious stimulation. This indicates higher-level pain processing capabilities in preterm infants from an early age.
Area of Science:
- Neuroscience
- Developmental Biology
- Pediatrics
Background:
- Understanding pain processing in premature infants is crucial for neonatal care.
- Previous research has not definitively established cortical pain processing in preterm neonates.
- Cerebral oxygenation changes can indicate brain activity in response to stimuli.
Purpose of the Study:
- To investigate whether premature infants exhibit cortical pain processing.
- To measure brain responses to noxious stimuli in preterm infants.
- To determine the developmental trajectory of cortical pain processing in preterm neonates.
Main Methods:
- Real-time near-infrared spectroscopy (NIRS) measured cerebral oxygenation.
- 18 infants aged 25-45 weeks postmenstrual age were studied.
- Noxious stimuli included routine heel lances; non-noxious stimuli were also applied.
Main Results:
- Noxious stimulation elicited a clear cortical response (increased total hemoglobin) from 25 weeks.
- Cortical responses were significantly greater in awake versus sleeping infants.
- In awake infants, response magnitude increased and latency decreased with age.
Conclusions:
- Noxious information reaches the preterm infant cortex by 25 weeks postmenstrual age.
- Preterm infants possess the capacity for higher-level pain processing.
- Early pain exposure may induce plasticity in the developing human brain.
Abstract:
Despite the recent increase in our understanding of the development of pain processing, it is still not known whether premature infants are capable of processing pain at a cortical level. In this study, changes in cerebral oxygenation over the somatosensory cortex were measured in response to noxious stimulation using real-time near-infrared spectroscopy in 18 infants aged between 25 and 45 weeks postmenstrual age. The noxious stimuli were heel lances performed for routine blood sampling; no blood tests were performed solely for the purpose of the study. Noxious stimulation produced a clear cortical response, measured as an increase in total hemoglobin concentration [HbT] in the contralateral somatosensory cortex, from 25 weeks (mean Delta[HbT] = 7.74 micromol/L; SE, 1.10). Cortical responses were significantly greater in awake compared with sleeping infants, with a mean difference of 6.63 micromol/L [95% confidence interval (CI) limits: 2.35, 10.91 micromol/L; mean age, 35.2 weeks]. In awake infants, the response in the contralateral somatosensory cortex increased with age (regression coefficient, 0.698 micromol/L/week; 95% CI limits: 0.132, 1.265 micromol/L/week) and the latency decreased with age (regression coefficient, -0.9861 micromol/L/week; 95% CI limits: -1.5361, -0.4361 micromol/L/week; age range, 25-38 weeks). The response was modality specific because no response was detected after non-noxious stimulation of the heel, even when accompanied by reflex withdrawal of the foot. We conclude that noxious information is transmitted to the preterm infant cortex from 25 weeks, highlighting the potential for both higher-level pain processing and pain-induced plasticity in the human brain from a very early age.
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