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治疗败血症性新生儿脑病的低温疗法:一项回顾性队列研究。

Therapeutic hypothermia for neonatal encephalopathy with sepsis: a retrospective cohort study.

机构信息

Newborn Services, Auckland City Hospital, Auckland, New Zealand.

Neonatal Medicine, Women's and Children's Hospital, Adelaide, South Australia, Australia.

出版信息

BMJ Paediatr Open. 2022 Mar;6(1). doi: 10.1136/bmjpo-2022-001420.

DOI:10.1136/bmjpo-2022-001420
PMID:36053591
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8943717/
Abstract

OBJECTIVE

Neonatal encephalopathy remains a major cause of infant mortality and neurodevelopmental impairment. Infection may exacerbate brain injury and mitigate the effect of therapeutic hypothermia (TH). Additionally, infants with sepsis treated with TH may be at increased risk of adverse effects. This study aimed to review the clinical characteristics and outcomes for infants with sepsis treated with TH.

DESIGN AND SETTING

Retrospective cohort study of infants treated with TH within Australia and New Zealand.

PATIENTS

1522 infants treated with TH, including 38 with culture-positive sepsis from 2014 to 2018.

INTERVENTION

Anonymised retrospective review of data from Australian and New Zealand Neonatal Network. Infants with culture-positive sepsis within 48 hours were compared with those without sepsis.

MAIN OUTCOME MEASURES

Key outcomes include in-hospital mortality, intensive care support requirements and length of stay.

RESULTS

Overall the rate of mortality was similar between the groups (13% vs 13%). Infants with sepsis received a higher rate of mechanical ventilation (89% vs 70%, p=0.01), high-frequency oscillatory ventilation (32% vs 13%, p=0.003) and inhaled nitric oxide for persistent pulmonary hypertension (38% vs 16%, p<0.001). Additionally, the sepsis group had a longer length of stay (20 vs 11 days, p<0.001).

CONCLUSION

Infants with sepsis treated with TH required significantly more respiratory support and had a longer length of stay. Although this may suggest a more severe illness the rate of mortality was similar. Further research is warranted to review the neurodevelopmental outcomes for these infants.

摘要

目的

新生儿脑病仍然是婴儿死亡和神经发育障碍的主要原因。感染可能会加重脑损伤,并减轻治疗性低体温(TH)的效果。此外,接受 TH 治疗的败血症婴儿可能会增加不良事件的风险。本研究旨在回顾接受 TH 治疗的败血症婴儿的临床特征和结局。

设计和设置

在澳大利亚和新西兰进行的接受 TH 治疗的婴儿的回顾性队列研究。

患者

2014 年至 2018 年间,1522 名接受 TH 治疗的婴儿,包括 38 名培养阳性败血症婴儿。

干预

对澳大利亚和新西兰新生儿网络的数据进行匿名回顾性审查。将 48 小时内培养阳性败血症的婴儿与无败血症的婴儿进行比较。

主要观察结果

主要结局包括院内死亡率、重症监护支持需求和住院时间。

结果

总体而言,两组死亡率相似(13% vs 13%)。败血症婴儿接受机械通气的比例更高(89% vs 70%,p=0.01)、高频振荡通气的比例更高(32% vs 13%,p=0.003)和吸入性一氧化氮治疗持续性肺动脉高压的比例更高(38% vs 16%,p<0.001)。此外,败血症组的住院时间更长(20 天 vs 11 天,p<0.001)。

结论

接受 TH 治疗的败血症婴儿需要更多的呼吸支持,且住院时间更长。尽管这可能表明病情更严重,但死亡率相似。需要进一步研究来评估这些婴儿的神经发育结局。

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本文引用的文献

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Current Therapies for Neonatal Hypoxic-Ischaemic and Infection-Sensitised Hypoxic-Ischaemic Brain Damage.新生儿缺氧缺血性及感染致敏性缺氧缺血性脑损伤的当前治疗方法
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Severe Pulmonary Hemorrhage in a Neonate With Hypoxic Ischemic Encephalopathy and Sepsis Managed on Extracorporeal Membrane Oxygenation.新生儿缺氧缺血性脑病合并脓毒症行体外膜肺氧合治疗后发生严重肺出血
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Hypothermia is not therapeutic in a neonatal piglet model of inflammation-sensitized hypoxia-ischemia.在炎症敏感型缺氧缺血新生仔猪模型中,低温治疗没有效果。
Pediatr Res. 2022 May;91(6):1416-1427. doi: 10.1038/s41390-021-01584-6. Epub 2021 May 28.
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Association of Routinely Measured Proinflammatory Biomarkers With Abnormal MRI Findings in Asphyxiated Neonates Undergoing Therapeutic Hypothermia.接受治疗性低温治疗的窒息新生儿中常规检测的促炎生物标志物与MRI异常结果的关联。
Front Pediatr. 2021 Mar 29;9:624652. doi: 10.3389/fped.2021.624652. eCollection 2021.
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Trends in the incidence and management of hypoxic-ischaemic encephalopathy in the therapeutic hypothermia era: a national population study.治疗性低体温时代缺氧缺血性脑病的发病和治疗趋势:一项全国性人群研究。
Arch Dis Child Fetal Neonatal Ed. 2021 Sep;106(5):529-534. doi: 10.1136/archdischild-2020-320902. Epub 2021 Mar 8.
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Changing clinical characteristics of infants treated for hypoxic-ischaemic encephalopathy in England, Wales and Scotland: a population-based study using the National Neonatal Research Database.改变英格兰、威尔士和苏格兰接受缺氧缺血性脑病治疗的婴儿的临床特征:一项使用国家新生儿研究数据库的基于人群的研究。
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PCR for the detection of pathogens in neonatal early onset sepsis.PCR 检测新生儿早发性败血症中的病原体。
PLoS One. 2020 Jan 24;15(1):e0226817. doi: 10.1371/journal.pone.0226817. eCollection 2020.
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Acute LPS sensitization and continuous infusion exacerbates hypoxic brain injury in a piglet model of neonatal encephalopathy.急性 LPS 致敏和持续输注加重新生脑病猪模型的缺氧性脑损伤。
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Early Pro-inflammatory Microglia Activation After Inflammation-Sensitized Hypoxic-Ischemic Brain Injury in Neonatal Rats.新生大鼠炎症致敏性缺氧缺血性脑损伤后早期促炎性小胶质细胞激活
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Management of Neonates Born at ≥35 0/7 Weeks' Gestation With Suspected or Proven Early-Onset Bacterial Sepsis.胎龄≥35 周的疑似或确诊早发性细菌性败血症新生儿的处理。
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