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对接受治疗性低温治疗的儿童进行早期和持续监测以预防可能出现的感染性并发症的必要性。

Necessity of early and continuous monitoring for possible infectious complications in children undergoing therapeutic hypothermia.

作者信息

Brandt Jennifer B, Steiner Sabine, Schlager Gerald, Sadeghi Kambis, Vargha Regina, Golej Johann, Hermon Michael

机构信息

Division of Neonatology, Paediatric Intensive Care & Neuropaediatrics, Department of Paediatric and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.

Department of Anaesthesiology, Intensive Care and Pain Therapy, Hospital of St. John of God, Vienna, Austria.

出版信息

Acta Paediatr. 2021 Mar;110(3):805-810. doi: 10.1111/apa.15506. Epub 2020 Aug 12.

DOI:10.1111/apa.15506
PMID:33074577
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7984159/
Abstract

AIM

Since therapeutic hypothermia (TH) is known for its inhibitory effects on leucocyte migration and cytokine synthesis, our aim was to underline the necessity of early monitoring for potential immunomodulatory risks.

METHODS

Using a 13-year retrospective case-control study at the paediatric intensive care unit (PICU) of the Medical University in Vienna, all newborn infants and children receiving TH were screened and compared with a diagnosis-matched control group undergoing conventional normothermic treatment (NT). TH was accomplished by using a non-invasive cooling device. Target temperature was 32-34°C. Children with evident infections, a medical history of an immunodeficiency or undergoing immunosuppressive therapy, were excluded.

RESULTS

During the observational period, 108 patients were screened, 27 of which underwent TH. Culture-proven infections occurred in 22% of the TH group compared with 4% of the normothermic controls (P = .1). From the second day following PICU admission, median C-reactive protein (CRP) values were higher in the TH group (day two P = .002, day three P = .0002, day six P = .008).

CONCLUSION

Children undergoing TH showed earlier and higher increases in CRP levels when compared to normothermic controls. These data underline the necessity of early and continuous monitoring for possible infectious complications.

摘要

目的

鉴于治疗性低温(TH)对白细胞迁移和细胞因子合成具有抑制作用,我们的目的是强调早期监测潜在免疫调节风险的必要性。

方法

在维也纳医科大学儿科重症监护病房(PICU)进行了一项为期13年的回顾性病例对照研究,对所有接受TH的新生儿和儿童进行筛查,并与接受传统常温治疗(NT)的诊断匹配对照组进行比较。TH通过使用无创冷却装置实现。目标温度为32-34°C。排除有明显感染、免疫缺陷病史或正在接受免疫抑制治疗的儿童。

结果

在观察期内,共筛查了108例患者,其中27例接受了TH。TH组中经培养证实的感染发生率为22%,而常温对照组为4%(P = 0.1)。从入住PICU的第二天起,TH组的C反应蛋白(CRP)中位数水平更高(第二天P = 0.002,第三天P = 0.0002,第六天P = 0.008)。

结论

与常温对照组相比,接受TH的儿童CRP水平升高更早且更高。这些数据强调了早期和持续监测可能的感染并发症的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dc1/7984159/2053519c8169/APA-110-805-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dc1/7984159/aad897c59e57/APA-110-805-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dc1/7984159/c949919ec6fa/APA-110-805-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dc1/7984159/2053519c8169/APA-110-805-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dc1/7984159/aad897c59e57/APA-110-805-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dc1/7984159/c949919ec6fa/APA-110-805-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dc1/7984159/2053519c8169/APA-110-805-g001.jpg

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本文引用的文献

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Am J Perinatol. 2020 Oct;37(12):1264-1270. doi: 10.1055/s-0039-1693466. Epub 2019 Jul 25.
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Major causes of death in preterm infants in selected hospitals in Ethiopia (SIP): a prospective, cross-sectional, observational study.选定埃塞俄比亚医院早产儿的主要死亡原因(SIP):一项前瞻性、横断面、观察性研究。
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Therapeutic Hypothermia in Neonatal Hypoxic-Ischemic Encephalopathy.
新生儿缺氧缺血性脑病的治疗性低温。
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Outcome of Infants with Therapeutic Hypothermia after Perinatal Asphyxia and Early-Onset Sepsis.围产期窒息和早发性败血症患儿亚低温治疗的结局。
Neonatology. 2019;115(2):127-133. doi: 10.1159/000493358. Epub 2018 Nov 12.
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Study protocol: optimising newborn nutrition during and after neonatal therapeutic hypothermia in the United Kingdom: observational study of routinely collected data using propensity matching.研究方案:在英国新生儿治疗性低温期间及之后优化新生儿营养:使用倾向匹配对常规收集数据进行的观察性研究。
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Therapeutic hypothermia after paediatric cardiac arrest: Pooled randomized controlled trials.儿科心搏骤停后治疗性低温:汇总随机对照试验。
Resuscitation. 2018 Dec;133:101-107. doi: 10.1016/j.resuscitation.2018.09.011. Epub 2018 Oct 3.
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