Diagnostic value of interleukin-6 and C-reactive protein on early onset bacterial infection in preterm neonates with respiratory distress

被引:5
作者
Rego, Maria Aparecida C. [1 ]
Martinez, Francisco Eulogio [1 ]
Elias, Jorge, Jr. [2 ]
Mussi-Pinhata, Marisa Marcia [1 ]
机构
[1] Univ Sao Paulo, Fac Med Ribeirao Preto, Dept Pediat, BR-14049900 Ribeirao Preto, SP, Brazil
[2] Univ Sao Paulo, Fac Med Ribeirao Preto, Dept Radiol, BR-14049900 Ribeirao Preto, SP, Brazil
关键词
C-reactive protein; cytokine; early onset neonatal sepsis; interleukin-6; neonatal respiratory distress syndrome; neonatal sepsis; preterm infant; TUMOR-NECROSIS-FACTOR; IMMEDIATE POSTNATAL-PERIOD; FACTOR-ALPHA; ILLNESS SEVERITY; NEWBORN-INFANTS; PLASMA-LEVELS; SEPSIS; PROCALCITONIN; MARKERS; RECEPTORS;
D O I
10.1515/JPM.2010.071
中图分类号
R71 [妇产科学];
学科分类号
100211 [妇产科学];
摘要
Aims: To evaluate the C-reactive protein (CRP) and interleukin-6 (IL-6) as diagnostic tools for early onset infection in preterm infants with early respiratory distress (RD). Methods: CRP and IL-6 were quantified at identification of RD and 24 h after in 186 newborns. Effects of maternal hypertension, mode of delivery, Apgar score, birth weight, gestational age, mechanical ventilation, being small for gestational age (SGA), and the presence of infection were analyzed. Results: Forty-four infants were classified as infected, 42 as possibly infected, and 100 as uninfected. Serum levels of IL-6 (0 h), CRP (0 h), and CRP (24 h), but not IL-6 (24 h) were significantly higher in infected infants compared to the remaining groups. The best test for identification of infection was the combination of IL-6 (0 h) 36 pg/dL and/or CRP (24 h) 0.6 mg/dL, which yielded 93% sensitivity and 37% specificity. The presence of infection and vaginal delivery independently increased IL-6 (0 h), CRP (0 h) and CRP (24 h) levels. Being SGA also increased the CRP (24 h) levels. IL-6 (24 h) was independently increased by mechanical ventilation. Conclusions: The combination of IL-6 (0 h) and/or CRP (24 h) is helpful for excluding early onset infection in preterm infants with RD but the poor specificity limits its potential benefit as a diagnostic tool.
引用
收藏
页码:527 / 533
页数:7
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