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J Appl Physiol (March 19, 2009). doi:10.1152/japplphysiol.91156.2008
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Submitted on August 28, 2008
Revised on March 10, 2009
Accepted on March 12, 2009

Cerebral metabolic rate of oxygen and amplitude-integrated electroencephalography during early reperfusion after hypoxia-ischemia in piglets

Kenneth M. Tichauer1*, Jonathan T. Elliott1, Jennifer A. Hadway1, Ting-Yim Lee2, and Keith St. Lawrence1

1 Lawson Health Research Institute
2 Robarts Research Institute

* To whom correspondence should be addressed. E-mail: ktichaue{at}lawsonimaging.ca.

The therapeutic window following perinatal hypoxia-ischemia is brief and early clinical signs of injury can be subtle. Electroencephalography (EEG) represents the most promising early diagnostic of hypoxia-ischemia; however, some studies have questioned the sensitivity and specificity of EEG. The current study investigated the use of both near-infrared spectroscopy (NIRS) measurements of the cerebral metabolic rate of oxygen (CMRO2) and amplitude-integrated EEG (aEEG) to detect the severity of hypoxia-ischemia after 1 h of reperfusion in newborn piglets (10 insult, 3 controls). The CMRO2 was measured before and after 1 h of reperfusion from hypoxia-ischemia - the duration of which was varied from piglet to piglet with a range of 3-24 min - under fentanyl/nitrous oxide anesthesia to mimic awake-like levels of cerebral metabolism. Electroencephalography data were collected throughout the study. On average, the CMRO2 and mean aEEG background signal were significantly depressed following the insult (p < 0.05). Mean CMRO2 and mean aEEG background were 2.61 ± 0.11 mlO2.min-1.100g-1 and 20.4 ± 2.7 µV prior to the insult and 1.58 ± 0.09 mlO2•min-1.100g-1 and 11.8 ± 2.9 µV after 1 h of reperfusion, respectively. Both CMRO2 and aEEG displayed statistically significant correlations with duration of ischemia (p < 0.05; r = 0.71 and r = 0.89, respectively); however, only CMRO2 was sensitive to milder injuries (< 5 min). This study highlights the potential for combining NIRS measures of CMRO2 with EEG in the neonatal intensive care unit to improve early detection of perinatal hypoxia-ischemia.







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