Viremia as a predictor of absence of serious bacterial infection in children with fever without source

被引:1
|
作者
Galetto-Lacour, Annick [1 ]
Cordey, Samuel [2 ]
Papis, Sebastien [3 ]
Mardegan, Chiara [3 ]
Luterbacher, Fanny [3 ]
Combescure, Christophe [4 ]
Lacroix, Laurence [1 ]
Gervaix, Alain [1 ]
Kaiser, Laurent [2 ,5 ]
Posfay-Barbe, Klara M. [3 ,6 ]
L'Huillier, Arnaud G. [2 ,3 ,6 ]
机构
[1] Geneva Univ Hosp & Fac Med, Dept Women Child & Adolescent Med, Div Pediat Emergencies, Geneva, Switzerland
[2] Geneva Univ Hosp & Fac Med, Diagnost Dept, Lab Virol, Geneva, Switzerland
[3] Geneva Univ Hosp & Fac Med, Dept Women Child & Adolescent Med, Div Gen Pediat, Geneva, Switzerland
[4] Geneva Univ Hosp & Fac Med, Dept Hlth & Community Med, Div Clin Epidemiol, Geneva, Switzerland
[5] Geneva Univ Hosp & Fac Med, Dept Med, Div Infect Dis, Geneva, Switzerland
[6] Geneva Univ Hosp & Fac Med, Dept Women Child & Adolescent Med, Pediat Infect Dis Unit, Geneva, Switzerland
关键词
Biomarker; Viral systemic infection; Prognostic accuracy; C-reactive protein; Procalcitonin; Sensitivity; Predictor; Negative predictive value; FEBRILE INFANTS; PRACTICE GUIDELINE; YOUNG-CHILDREN; INFLUENZA-A; MANAGEMENT; RISK; PROCALCITONIN; SCORE; AGE; DIAGNOSIS;
D O I
10.1007/s00431-022-04690-7
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Most children with fever without source (FWS) require diagnostic laboratory tests to exclude a serious bacterial infection (SBI), often followed by admission and empirical antibiotics. As febrile children with a viral infection are less likely to have a SBI, identifying patients with systemic viral infection could contribute to exclude SBI. We evaluated whether the presence of virus in the blood could be used as a biomarker to rule out SBI. Children < 3 years old with FWS were prospectively enrolled and had real-time (reverse-transcription) PCR performed on the blood for adenovirus, enterovirus, parechovirus, and HHV6. 20/135 patients had SBI, and in 47/135, at least one virus was detected in the blood. Viremia had a higher sensitivity and negative predictive value (90% and 96%) to rule out SBI compared to CRP (65% and 93%) and PCT (55% and 90%). The odds ratio (OR) for the presence of SBI among non-viremic patients was 5.8 (p = 0.0225), compared to 5.5 for CRP >= 40 mg/l (p = 0.0009) and 3.7 for PCT >= 0.5 ng/mL (0.0093). This remained significant after adjusting for CRP and PCT (OR 5.6 and 5.9, respectively; p = 0.03 for both). Area under the ROC curve for CRP and PCT were 0.754 and 0.779, respectively, but increased to 0.803 and 0.832, respectively, when combined with viremia. Conclusion: The presence of viremia had a better performance than commonly used biomarkers to rule-out SBI and could potentially be used in conjunction with CRP and/or PCT in the evaluation of children with FWS. Larger studies should evaluate the role of point-of-care testing of viruses by (revere-transcription) PCR in the plasma in management algorithms of children with FWS.
引用
收藏
页码:941 / 947
页数:7
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