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经粪便挥发性化合物分析对早产儿迟发性非导管相关性败血症的临床前检测:一项前瞻性、多中心队列研究。

Preclinical Detection of Non-catheter Related Late-onset Sepsis in Preterm Infants by Fecal Volatile Compounds Analysis: A Prospective, Multi-center Cohort Study.

机构信息

From the Department of Pediatric Gastroenterology, Emma Children's Hospital, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands.

Department of Pediatric Gastroenterology, Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands.

出版信息

Pediatr Infect Dis J. 2020 Apr;39(4):330-335. doi: 10.1097/INF.0000000000002589.

Abstract

BACKGROUND

Late onset sepsis (LOS) in preterm infants is preceded by fecal volatile organic compound (VOC) alterations, suggesting an etiologic role of gut microbiota in LOS rather than being primarily caused by central venous catheters (CVC). To increase our knowledge about the involvement of the gut microbiota in LOS, we analyzed fecal samples from septic infants without a CVC.

METHODS

In this prospective multicenter study, fecal samples were collected daily from all infants born at ≤30 weeks gestation. Fecal VOC profiles up to 3 days prior to sepsis onset from infants with non-catheter-related LOS were compared with profiles from non-septic controls by means of High-Field Asymmetric Waveform Ion Mobility Spectrometry.

RESULTS

In total, 104 fecal samples were analyzed. Fecal VOC profiles allowed for discrimination between non-catheter-related LOS cases (n = 24) and matched controls (n = 25). Discriminative accuracy increased after focusing on center of origin (area under the curve, sensitivity, specificity; 0.95, 100%, 83%) and after focusing on LOS cases caused by Staphylococcus epidermidis (0.95, 100%, 78%), the most cultured pathogen (n = 11).

CONCLUSIONS

Fecal VOC profiles of preterm LOS infants without a CVC differed from matched controls underlining the increasing notion that aberrations in gut microbiota composition and activity may play a role in LOS etiology.

摘要

背景

早产儿晚发性败血症(LOS)之前存在粪便挥发性有机化合物(VOC)改变,这表明肠道微生物群在 LOS 中的发病机制作用,而不是主要由中心静脉导管(CVC)引起的。为了增加我们对肠道微生物群在 LOS 中作用的了解,我们分析了无 CVC 的败血症婴儿的粪便样本。

方法

在这项前瞻性多中心研究中,每天收集所有≤30 周胎龄出生的婴儿的粪便样本。通过高场非对称波形离子迁移谱法,比较 LOS 患儿粪便样本中与非脓毒症对照组相比,在 LOS 发病前 3 天内的粪便 VOC 谱。

结果

共分析了 104 个粪便样本。粪便 VOC 谱可区分非导管相关性 LOS 病例(n=24)和匹配对照组(n=25)。将重点放在起源中心(曲线下面积、灵敏度、特异性;0.95、100%、83%)和聚焦于表皮葡萄球菌引起的 LOS 病例(0.95、100%、78%)后,诊断准确性增加,表皮葡萄球菌是最常培养的病原体(n=11)。

结论

无 CVC 的早产儿 LOS 婴儿的粪便 VOC 谱与匹配的对照组不同,这进一步表明肠道微生物群组成和活性的异常可能在 LOS 的发病机制中起作用。

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