Increased Inspired Oxygen in the First Hours of Life is Associated with Adverse Outcome in Newborns Treated for Perinatal Asphyxia with Therapeutic Hypothermia

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• 作者：Hemmen Sabir ; MD¹ ; ⁴ ; Sally Jary ; MSc¹ ; ² ; James Tooley ; MRCPCH² ; Xun Liu ; PhD¹ ; Marianne Thoresen ; MD ; PhD¹ ; ³ ; ^{Marianne.thoresen@bristol.ac.uk}
• 关键词：AUC ; Area under the curve ; Bayley II ; Bayley Scales of Newborn Development II ; CBF ; Cerebral blood flow ; Fio2 ; Fraction of inspiratory oxygen ; MDI ; Mental Development Index ; PDI ; Psychomotor Development Index ; Tcso2 ; Transcutaneous peripheral saturation
• 刊名：The Journal of Pediatrics
• 出版年：2012
• 出版时间：September, 2012
• 年：2012
• 卷：161
• 期：3
• 页码：409-416
• 全文大小：643 K

文摘

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Objective

To assess whether increased inspired oxygen and/or hypocarbia during the first 6 hours of life are associated with adverse outcome at 18 months in term neonates treated with therapeutic hypothermia.

Study design

Blood gas values and ventilatory settings were monitored hourly in 61 newborns for 6 hours after birth. We investigated if there was an association between increased inspired oxygen and/or hypocarbia and adverse outcome (death or disability by Bayley Scales of Newborn Development II examination at 18-20 months).

Results

Hypothermia was started from 3 hours 45 minutes (10 minutes-10 hours) and median lowest Pco₂ level within the first 6 hours of life was 30 mm Hg (16.5-96 mm Hg). The median highest fraction of inspiratory oxygen within the first hour of life was 0.43 (0.21-1.00). The area under the curve fraction of inspiratory oxygen and Pao₂ for hours 1-6 of life was 0.23 (0.21-1.0) and 86 mm Hg (22-197 mm Hg), respectively. We did not find any association between any measures of hypocapnia and adverse outcome (P > .05), but increased inspired oxygen correlated with adverse outcome, even when excluding newborns with initial oxygenation failure (P < .05).

Conclusion

Increased fraction of inspired oxygen within the first 6 hours of life was significantly associated with?adverse outcome in newborns treated with therapeutic hypothermia following hypoxic ischemic encephalopathy.