2006
DOI: 10.1016/j.acpain.2006.08.033
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Biobehavioural reactivity to pain in preterm infants: A marker of neuromotor development

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Cited by 5 publications
(4 citation statements)
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References 26 publications
(27 reference statements)
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“…Unrelieved pain caused by invasive procedures is associated with adverse behavioral and biophysiologic outcomes such as increased heart rate, blood pressure, oxygen consumption, and stress hormone secretion, all of which cause marked fluctuation in intracranial pressure, possibly leading to intraventricular hemorrhage (IVH) and periventricular leukomalacia Holsti, Grunau, Oberlander, & Whitfield, 2004;Taddio, Shah, Gilbert-MacLeod, & Katz, 2002). Early and repeated exposure of preterm infants to pain may also have long-term cumulative sequelae, including prolonged structural and functional alterations in pain pathways that can last into adult life, permanently altering normal or common responses to pain (Abdulkader, Freer, Garry, Fleetwood-Walker, & McIntosh, 2008;Fitzgerald & Walker, 2009;Grunau, Whitfield, et al, 2006). Pain is also believed to be neurotoxic to hippocampal formation (Fitzgerald & Walker, 2009;Grunau et al, 2009;Thompson et al, 2008) and may have specific adverse effects on cognition, memory (Beauchamp et al, 2008;Grunau, Holsti, & Peters, 2006;Grunau et al, 2009), and motor development (Grunau et al, 2009;Holsti, Grunau, Oberlander, & Whitfield, 2005).…”
mentioning
confidence: 99%
“…Unrelieved pain caused by invasive procedures is associated with adverse behavioral and biophysiologic outcomes such as increased heart rate, blood pressure, oxygen consumption, and stress hormone secretion, all of which cause marked fluctuation in intracranial pressure, possibly leading to intraventricular hemorrhage (IVH) and periventricular leukomalacia Holsti, Grunau, Oberlander, & Whitfield, 2004;Taddio, Shah, Gilbert-MacLeod, & Katz, 2002). Early and repeated exposure of preterm infants to pain may also have long-term cumulative sequelae, including prolonged structural and functional alterations in pain pathways that can last into adult life, permanently altering normal or common responses to pain (Abdulkader, Freer, Garry, Fleetwood-Walker, & McIntosh, 2008;Fitzgerald & Walker, 2009;Grunau, Whitfield, et al, 2006). Pain is also believed to be neurotoxic to hippocampal formation (Fitzgerald & Walker, 2009;Grunau et al, 2009;Thompson et al, 2008) and may have specific adverse effects on cognition, memory (Beauchamp et al, 2008;Grunau, Holsti, & Peters, 2006;Grunau et al, 2009), and motor development (Grunau et al, 2009;Holsti, Grunau, Oberlander, & Whitfield, 2005).…”
mentioning
confidence: 99%
“…Our findings likely reflect a critical immaturity of the autonomic nervous system in sick preterm infants 46. Recent studies showed reduced physiologic responses to noxious stimuli in preterm infants,47-50 including reduced autonomic (especially sympathetic) activity and central behavioral responses 51. Recent cerebral NIRS studies demonstrated cortical responses to noxious stimuli in infants as young as 25 weeks' gestation,28,52 which decreased significantly with lower gestational age.…”
Section: Discussionmentioning
confidence: 54%
“…This finding justifies the birth term range chosen in our study to homogenise the preterm population. Furthermore, Grunau et al (23) postulated that the severity of autonomic dysfunction during the neonatal period could be predictive of a poor neurologic outcome in the extreme preterm population. All this data was in favour of overall alteration of central and autonomic nervous system development secondary to preterm birth.…”
Section: Discussionmentioning
confidence: 99%