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高偏差气体流量增加了通气早产儿肺损伤。

High bias gas flows increase lung injury in the ventilated preterm lamb.

机构信息

Liggins Institute, University of Auckland, New Zealand.

出版信息

PLoS One. 2012;7(10):e47044. doi: 10.1371/journal.pone.0047044. Epub 2012 Oct 8.

DOI:10.1371/journal.pone.0047044
PMID:23056572
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3466239/
Abstract

BACKGROUND

Mechanical ventilation of preterm babies increases survival but can also cause ventilator-induced lung injury (VILI), leading to the development of bronchopulmonary dysplasia (BPD). It is not known whether shear stress injury from gases flowing into the preterm lung during ventilation contributes to VILI.

METHODS

Preterm lambs of 131 days' gestation (term = 147 d) were ventilated for 2 hours with a bias gas flow of 8 L/min (n = 13), 18 L/min (n = 12) or 28 L/min (n = 14). Physiological parameters were measured continuously and lung injury was assessed by measuring mRNA expression of early injury response genes and by histological analysis. Control lung tissue was collected from unventilated age-matched fetuses. Data were analysed by ANOVA with a Tukey post-hoc test when appropriate.

RESULTS

High bias gas flows resulted in higher ventilator pressures, shorter inflation times and decreased ventilator efficiency. The rate of rise of inspiratory gas flow was greatest, and pulmonary mRNA levels of the injury markers, EGR1 and CTGF, were highest in lambs ventilated with bias gas flows of 18 L/min. High bias gas flows resulted in increased cellular proliferation and abnormal deposition of elastin, collagen and myofibroblasts in the lung.

CONCLUSIONS

High ventilator bias gas flows resulted in increased lung injury, with up-regulation of acute early response genes and increased histological lung injury. Bias gas flows may, therefore, contribute to VILI and BPD.

摘要

背景

对早产儿进行机械通气可提高存活率,但也可能导致呼吸机相关性肺损伤(VILI),从而引发支气管肺发育不良(BPD)。目前尚不清楚通气时气体流入早产儿肺部产生的切变力损伤是否会导致 VILI。

方法

对 131 日龄(足月 = 147 日)的早产羔羊进行 2 小时通气,偏置气体流量分别为 8 L/min(n = 13)、18 L/min(n = 12)或 28 L/min(n = 14)。连续测量生理参数,并通过测量早期损伤反应基因的 mRNA 表达和组织学分析评估肺损伤。从未通气的同龄胎儿中采集对照肺组织。数据通过方差分析和 Tukey 事后检验进行分析。

结果

高偏置气体流量导致呼吸机压力更高、充气时间更短和呼吸机效率降低。吸气气体流量的上升率最大,以 18 L/min 偏置气体流量通气的羔羊肺中损伤标志物 EGR1 和 CTGF 的 mRNA 水平最高。高偏置气体流量导致肺细胞增殖增加,弹性蛋白、胶原和肌成纤维细胞在肺中异常沉积。

结论

高呼吸机偏置气体流量导致肺损伤增加,急性早期反应基因上调,组织学肺损伤增加。因此,偏置气体流量可能导致 VILI 和 BPD。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24a5/3466239/aeb4607b91ae/pone.0047044.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24a5/3466239/85a8ca14d385/pone.0047044.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24a5/3466239/665ef72bc696/pone.0047044.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24a5/3466239/aeb4607b91ae/pone.0047044.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24a5/3466239/85a8ca14d385/pone.0047044.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24a5/3466239/665ef72bc696/pone.0047044.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24a5/3466239/aeb4607b91ae/pone.0047044.g003.jpg

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