Department of Neonatology, Oslo University Hospital, Norway.
Department of Pediatric Research, University of Oslo & Ann and Robert H. Lurie Children's Hospital of Chicago Northwestern University Feinberg School of Medicine, Norway.
Semin Fetal Neonatal Med. 2020 Apr;25(2):101078. doi: 10.1016/j.siny.2020.101078. Epub 2020 Jan 17.
The premature infant is to some extent protected from hypoxia, however defense against hyperoxia is poorly developed. The optimal assessment of oxygenation is to measure oxygen delivery and extraction. At the bedside PaO and SpO are approximations of oxygenation at the tissue level. After birth asphyxia it is crucial to know whether or not to give oxygen supplementation, when, how much, and for how long. Oxygen saturation targets in the delivery room have been studied, but the optimal targets might still be unknown because factors like gender and delayed cord clamping influence saturation levels. However, SpO > 80% at 5 min of age is associated with favorable long term outcome in preterm babies. Immature infants most often need oxygen supplementation beyond the delivery room. Predefined saturation levels, and narrow alarm limits together with the total oxygen exposure may impact on development of oxygen related diseases like ROP and BPD. Hyperoxia is a strong trigger for genetic and epigenetic changes, contributing to the development of these conditions and perhaps lifelong changes.
早产儿在某种程度上受到缺氧的保护,然而,其对高氧的防御能力尚未完全发育。最佳的氧合评估方法是测量氧输送和氧摄取。在床边,PaO 和 SpO 是组织水平氧合的近似值。出生后窒息,关键是要知道是否需要补充氧气,何时、多少、多长时间。分娩室中的氧饱和度目标已经进行了研究,但由于性别和延迟脐带结扎等因素会影响饱和度水平,因此最佳目标可能仍未知。然而,早产儿在出生后 5 分钟时的 SpO > 80%与良好的长期预后相关。不成熟的婴儿通常需要在分娩室外补充氧气。预设的饱和度水平和狭窄的报警限制以及总氧气暴露可能会影响与 ROP 和 BPD 等氧气相关疾病的发展。高氧是遗传和表观遗传变化的强烈触发因素,导致这些情况的发展,并可能导致终身变化。