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Diagnosis of late onset neonatal sepsis with cytokines adhesion molecule and C-reactive protein in preterm very low birthweight infants

机译:细胞因子黏附分子和C反应蛋白对早产新生儿败血症的诊断

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摘要

AIMS—To evaluate the commonly used markers—namely IL-6, TNFα, IL-1β, C-reactive protein and E-selectin for identification of late onset neonatal sepsis; to define the optimal cutoff value for each marker in preterm neonates; to assess whether these markers could assist in early discontinuation of antibiotics in non-infected cases; and to delineate the profile of these markers during systemic infection and in relation to successful treatment.
METHODS—Very low birthweight infants in whom clinical sepsis was suspected when they were >72 hours of age were eligible for study. A full sepsis screen was performed in each episode. Cytokines, C-reactive protein, and E-selectin were serially measured on days 0 (at the time of sepsis evaluation), 1, 2, 4 and 7. The optimal cutoff value for each marker was calculated after minimising the number of misclassified episodes over all possible cutoff values for days 0 and 1. The sensitivity, specificity, positive and negative predictive values for each test and combination of tests for predicting systemic infection were also determined.
RESULTS—One hundred and one episodes of suspected clinical sepsis were investigated in 68 infants. Forty five episodes were proved to be infections. The optimal cutoff values were IL-6 31 pg/ml, TNFα 17 pg/ml, IL-1β 1 pg/ml, C reactive protein 12 mg/l and E-selectin 174 ng/ml. IL-6 had the highest sensitivity (89%) and negative predictive value (91%) for detecting late onset infection on day 0. However, between 24 and 48 hours of onset, C-reactive protein was the best single marker, with an overall sensitivity and specificity of 84% and 96%, respectively. The use of serial and multiple markers in the first 48 hours further enhanced the sensitivity and specificity of these tests. Performing IL-6 and C-reactive protein on day 0, together with either TNFα on day 1 or C-reactive protein on day 2, showed the best overall sensitivity (98%) and specificity (91%) for the diagnosis of late onset infection.
CONCLUSIONS—Optimal cutoff values for these markers in detecting late onset systemic infection in very low birthweight infants have been defined. Withholding antibiotic treatment at the onset of infection could be fatal and is not recommended, but the concomitant use of IL-6 and C-reactive protein or TNFα should allow antimicrobial treatment to be discontinued at 48 hours without waiting for microbiological results, provided that the infants are in good clinical condition.

Keywords: C-reactive protein; E-selectin; interleukin 1β; interleukin-6; tumour necrosis factor α; very low birthweight
机译:目的:评估常用的标志物,即IL-6,TNFα,IL-1β,C反应蛋白和E-选择素,以鉴定迟发性新生儿败血症;为早产儿的每个标记物定义最佳的临界值;评估这些标志物是否可以在未感染的病例中帮助抗生素的早期停用;方法
方法-怀疑是年龄> 72小时的临床诊断为败血症的低出生体重低婴儿,符合研究条件。在每个发作中进行完整的败血症筛选。在第0天(脓毒症评估时),1、2、4和7天连续测量细胞因子,C反应蛋白和E-选择素。在将错误分类的发作次数降至最少之后,计算出每种标记物的最佳临界值在第0天和第1天的所有可能临界值上进行测定。还确定了每种测试和测试组合对预测系统性感染的敏感性,特异性,阳性和阴性预测值。
结果-一百零一集可疑临床对68名婴儿进行了败血症调查。事实证明四十五集是感染。最佳临界值是IL-6 31 pg / ml,TNFα17 pg / ml,IL-1β1 pg / ml,C反应蛋白12 mg / l和E-选择素174 ng / ml。 IL-6在第0天检测迟发感染的敏感性最高(89%)和阴性预测值(91%)。然而,在发病​​24至48小时之间,C反应蛋白是最好的单一标志物,且总体敏感性和特异性分别为84%和96%。在开始的48小时内使用连续和多个标记物进一步提高了这些测试的灵敏度和特异性。在第0天进行IL-6和C反应蛋白的检测,在第1天与TNFα的检测或在第2天进行C反应的蛋白的检测,表明对迟发性疾病的诊断具有最佳的总体敏感性(98%)和特异性(91%)感染。
结论—已经确定了这些标志物在极低出生体重婴儿中发现迟发性全身感染的最佳临界值。在感染发作时停止抗生素治疗可能是致命的,因此不建议使用,但同时使用IL-6和C反应蛋白或TNFα可以在48小时内停止抗菌治疗,而无需等待微生物学结果,前提是

关键词:C反应蛋白E-选择素白介素1β;白介素6;肿瘤坏死因子α;出生体重很低

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