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本文引用的文献

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A Novel Framework for Phenotyping Children With Suspected or Confirmed Infection for Future Biomarker Studies.一种用于对疑似或确诊感染儿童进行表型分析以开展未来生物标志物研究的新型框架。
Front Pediatr. 2021 Jul 28;9:688272. doi: 10.3389/fped.2021.688272. eCollection 2021.
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Age- and sex-specific prevalence of serious bacterial infections in febrile infants ≤60 days, in Sweden.60 天内发热婴儿严重细菌感染的年龄和性别特异性流行率,瑞典。
Acta Paediatr. 2021 Nov;110(11):3069-3076. doi: 10.1111/apa.16043. Epub 2021 Jul 27.
3
Role of C reactive protein and procalcitonin in the diagnosis of lower respiratory tract infection in children in the outpatient setting.C反应蛋白和降钙素原在儿童门诊下呼吸道感染诊断中的作用
BMJ. 2021 Jun 11;373:n1409. doi: 10.1136/bmj.n1409.
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Etiology of Clinical Community-Acquired Pneumonia in Swedish Children Aged 1-59 Months with High Pneumococcal Vaccine Coverage-The TREND Study.瑞典1至59个月龄肺炎球菌疫苗高接种率儿童临床社区获得性肺炎的病因——趋势研究
Vaccines (Basel). 2021 Apr 14;9(4):384. doi: 10.3390/vaccines9040384.
5
Translation of a Host Blood RNA Signature Distinguishing Bacterial From Viral Infection Into a Platform Suitable for Development as a Point-of-Care Test.将宿主血液 RNA 特征从细菌感染到病毒感染的区分转化为适合开发即时检测的平台。
JAMA Pediatr. 2021 Apr 1;175(4):417-419. doi: 10.1001/jamapediatrics.2020.5227.
6
A Multi-mRNA Host-Response Molecular Blood Test for the Diagnosis and Prognosis of Acute Infections and Sepsis: Proceedings from a Clinical Advisory Panel.用于急性感染和脓毒症诊断及预后评估的多信使核糖核酸宿主反应分子血液检测:临床咨询小组会议纪要
J Pers Med. 2020 Dec 7;10(4):266. doi: 10.3390/jpm10040266.
7
C-Reactive Protein, Procalcitonin, and White Blood Count to Rule Out Neonatal Early-onset Sepsis Within 36 Hours: A Secondary Analysis of the Neonatal Procalcitonin Intervention Study.C 反应蛋白、降钙素原和白细胞计数用于 36 小时内排除新生儿早发性败血症:新生儿降钙素原干预研究的二次分析。
Clin Infect Dis. 2021 Jul 15;73(2):e383-e390. doi: 10.1093/cid/ciaa876.
8
Human Respiratory Syncytial Virus-Induced Immune Signature of Infection Revealed by Transcriptome Analysis of Clinical Pediatric Nasopharyngeal Swab Samples.人类呼吸道合胞病毒感染的免疫特征通过临床儿科鼻咽拭子样本的转录组分析揭示。
J Infect Dis. 2021 Mar 29;223(6):1052-1061. doi: 10.1093/infdis/jiaa468.
9
The Feasibility of Host Transcriptome Profiling as a Diagnostic Tool for Microbial Etiology in Childhood Cancer Patients with Febrile Neutropenia.宿主转录组分析作为发热性中性粒细胞减少症儿童癌症患者微生物病因学诊断工具的可行性。
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10
Diagnostic and Prognostic Value of IL-6 and sTREM-1 in SIRS and Sepsis in Children.IL-6 和 sTREM-1 在儿童全身炎症反应综合征和脓毒症中的诊断和预后价值。
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鉴别发热儿童病毒感染与细菌感染的新型生物标志物:临床实践管理的未来展望

Novel Biomarkers Differentiating Viral from Bacterial Infection in Febrile Children: Future Perspectives for Management in Clinical Praxis.

作者信息

Rhedin Samuel, Elfving Kristina, Berggren Anna

机构信息

Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, s-171 65 Stockholm, Sweden.

Sachs' Children and Youth Hospital, Södersjukhuset, s-118 61 Stockholm, Sweden.

出版信息

Children (Basel). 2021 Nov 20;8(11):1070. doi: 10.3390/children8111070.

DOI:10.3390/children8111070
PMID:34828783
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8623137/
Abstract

Differentiating viral from bacterial infections in febrile children is challenging and often leads to an unnecessary use of antibiotics. There is a great need for more accurate diagnostic tools. New molecular methods have improved the particular diagnostics of viral respiratory tract infections, but defining etiology can still be challenging, as certain viruses are frequently detected in asymptomatic children. For the detection of bacterial infections, time consuming cultures with limited sensitivity are still the gold standard. As a response to infection, the immune system elicits a cascade of events, which aims to eliminate the invading pathogen. Recent studies have focused on these host-pathogen interactions to identify pathogen-specific biomarkers (gene expression profiles), or "pathogen signatures", as potential future diagnostic tools. Other studies have assessed combinations of traditional bacterial and viral biomarkers (C-reactive protein, interleukins, myxovirus resistance protein A, procalcitonin, tumor necrosis factor-related apoptosis-inducing ligand) to establish etiology. In this review we discuss the performance of such novel diagnostics and their potential role in clinical praxis. In conclusion, there are several promising novel biomarkers in the pipeline, but well-designed randomized controlled trials are needed to evaluate the safety of using these novel biomarkers to guide clinical decisions.

摘要

区分发热儿童的病毒感染和细菌感染具有挑战性,且常常导致抗生素的不必要使用。非常需要更准确的诊断工具。新的分子方法改进了病毒呼吸道感染的特异性诊断,但确定病因仍可能具有挑战性,因为在无症状儿童中经常检测到某些病毒。对于细菌感染的检测,灵敏度有限且耗时的培养方法仍然是金标准。作为对感染的反应,免疫系统引发一系列事件,旨在消除入侵的病原体。最近的研究集中在这些宿主-病原体相互作用上,以识别病原体特异性生物标志物(基因表达谱)或“病原体特征”,作为未来潜在的诊断工具。其他研究评估了传统细菌和病毒生物标志物(C反应蛋白、白细胞介素、黏液病毒抗性蛋白A、降钙素原、肿瘤坏死因子相关凋亡诱导配体)的组合以确定病因。在本综述中,我们讨论了此类新型诊断方法的性能及其在临床实践中的潜在作用。总之,有几种有前景的新型生物标志物正在研发中,但需要精心设计的随机对照试验来评估使用这些新型生物标志物指导临床决策的安全性。