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产前暴露于脲原体属会加重支气管肺发育不良,与早产儿随后的长时间机械通气协同作用。

Antenatal exposure to Ureaplasma species exacerbates bronchopulmonary dysplasia synergistically with subsequent prolonged mechanical ventilation in preterm infants.

机构信息

Department of Neonatal Medicine and Pediatrics, Osaka Medical College, Osaka, Japan.

出版信息

Pediatr Res. 2012 Mar;71(3):267-73. doi: 10.1038/pr.2011.47. Epub 2012 Jan 18.

Abstract

INTRODUCTION

The presence of microorganisms in gastric fluid in neonates at birth is postulated to reflect antenatal infection and also to be associated with the development of bronchopulmonary dysplasia (BPD).

RESULTS

A logistic regression analysis, after controlling for other risk factors, indicated that Ureaplasma-positive infants were not at increased risk for moderate/severe BPD (adjusted odds ratio (OR): 2.58, 95% confidence interval (CI): 0.57-6.89, P = 0.12). However, the association between the presence of Ureaplasma species and the risk for moderate/severe BPD increased significantly in infants on mechanical ventilation (MV) ≥2 wk (adjusted OR: 4.17, 95% CI: 1.62-44.1, P = 0.009). An analysis using a lung injury marker indicated that Ureaplasma-positive infants with MV ≥2 wk, but not other infants, showed higher serum KL-6 levels in samples taken from cord blood, and that KL-6 levels increased time-dependently up to 4 wk of age.

DISCUSSION

Antenatal exposure to Ureaplasma species induces lung injury prior to birth and synergistically contributes to the development of BPD in infants requiring prolonged MV (≥2 wk).

METHODS

We recovered gastric fluid specimens from 122 infants with gestational age (GA) <29 wk or birth weight <1,000 g to investigate whether these microorganisms influence respiratory outcome of BPD. A PCR analysis was used to detect urease and 16S ribosomal RNA (rRNA) genes to classify neonates into Ureaplasma-positive or Ureaplasma-negative infants.

摘要

简介

人们推测,新生儿胃内液体中微生物的存在反映了产前感染,并与支气管肺发育不良(BPD)的发生有关。

结果

在控制了其他危险因素后,逻辑回归分析表明,解脲脲原体阳性婴儿发生中重度 BPD 的风险没有增加(校正比值比(OR):2.58,95%置信区间(CI):0.57-6.89,P=0.12)。然而,在接受机械通气(MV)≥2 周的婴儿中,解脲脲原体与中重度 BPD 风险之间的关联显著增加(校正 OR:4.17,95%CI:1.62-44.1,P=0.009)。使用肺损伤标志物的分析表明,在接受 MV≥2 周的解脲脲原体阳性婴儿中,但在其他婴儿中没有,在取自脐血的样本中,血清 KL-6 水平较高,并且 KL-6 水平在 4 周龄之前呈时间依赖性增加。

讨论

产前接触脲原体属微生物会在出生前引起肺损伤,并与需要长时间 MV(≥2 周)的婴儿发生 BPD 协同作用。

方法

我们从 122 名胎龄(GA)<29 周或出生体重<1000g 的婴儿中回收胃内液体标本,以研究这些微生物是否会影响 BPD 的呼吸结局。使用 PCR 分析检测尿素酶和 16S 核糖体 RNA(rRNA)基因,将新生儿分类为解脲脲原体阳性或解脲脲原体阴性婴儿。

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