Optimized lung expansion ventilation modulates ventilation-induced lung injury in preterm lambs.

IF 2.7 3区 医学 Q1 PEDIATRICS
Pediatric Pulmonology Pub Date : 2024-11-01 Epub Date: 2024-07-03 DOI:10.1002/ppul.27153
Tim Brokken, Matthias C Hütten, Daan R M G Ophelders, Charlotte van Gorp, Tim G A M Wolfs, Martin Wald
{"title":"Optimized lung expansion ventilation modulates ventilation-induced lung injury in preterm lambs.","authors":"Tim Brokken, Matthias C Hütten, Daan R M G Ophelders, Charlotte van Gorp, Tim G A M Wolfs, Martin Wald","doi":"10.1002/ppul.27153","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Preterm infants close to viability commonly require mechanical ventilation (MV) for respiratory distress syndrome. Despite commonly used lung-sparing ventilation techniques, rapid lung expansion during MV induces lung injury, a risk factor for bronchopulmonary dysplasia. This study investigates whether ventilation with optimized lung expansion is feasible and whether it can further minimize lung injury. Therefore, optimized lung expansion ventilation (OLEV) was compared to conventional volume targeted ventilation.</p><p><strong>Methods: </strong>Twenty preterm lambs were surgically delivered after 132 days of gestation. Nine animals were randomized to receive OLEV for 24 h, and seven received standard MV. Four unventilated animals served as controls (NV). Lungs were sampled for histological analysis at the end of the experimental period.</p><p><strong>Results: </strong>Ventilation with OLEV was feasible, resulting in a significantly higher mean ventilation pressure (0.7-1.3 mbar). Temporary differences in oxygenation between OLEV and MV did not reach clinically relevant levels. Ventilation in general tended to result in higher lung injury scores compared to NV, without differences between OLEV and MV. While pro-inflammatory tumor necrosis factor-α messenger RNA (mRNA) levels increased in both ventilation groups compared to NV, only animals in the MV group showed a higher number of CD45-positive cells in the lung. In contrast, mean (standard deviations) surfactant protein-B mRNA levels were significantly lower in OLEV, 0.63 (0.38) compared to NV 1.03 (0.32) (p = .023, one-way analysis of variance).</p><p><strong>Conclusion: </strong>In conclusion, a small reduction in pulmonary inflammation after 24 h of support with OLEV suggests potential to reduce preterm lung injury.</p>","PeriodicalId":19932,"journal":{"name":"Pediatric Pulmonology","volume":null,"pages":null},"PeriodicalIF":2.7000,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pediatric Pulmonology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1002/ppul.27153","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/7/3 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"PEDIATRICS","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: Preterm infants close to viability commonly require mechanical ventilation (MV) for respiratory distress syndrome. Despite commonly used lung-sparing ventilation techniques, rapid lung expansion during MV induces lung injury, a risk factor for bronchopulmonary dysplasia. This study investigates whether ventilation with optimized lung expansion is feasible and whether it can further minimize lung injury. Therefore, optimized lung expansion ventilation (OLEV) was compared to conventional volume targeted ventilation.

Methods: Twenty preterm lambs were surgically delivered after 132 days of gestation. Nine animals were randomized to receive OLEV for 24 h, and seven received standard MV. Four unventilated animals served as controls (NV). Lungs were sampled for histological analysis at the end of the experimental period.

Results: Ventilation with OLEV was feasible, resulting in a significantly higher mean ventilation pressure (0.7-1.3 mbar). Temporary differences in oxygenation between OLEV and MV did not reach clinically relevant levels. Ventilation in general tended to result in higher lung injury scores compared to NV, without differences between OLEV and MV. While pro-inflammatory tumor necrosis factor-α messenger RNA (mRNA) levels increased in both ventilation groups compared to NV, only animals in the MV group showed a higher number of CD45-positive cells in the lung. In contrast, mean (standard deviations) surfactant protein-B mRNA levels were significantly lower in OLEV, 0.63 (0.38) compared to NV 1.03 (0.32) (p = .023, one-way analysis of variance).

Conclusion: In conclusion, a small reduction in pulmonary inflammation after 24 h of support with OLEV suggests potential to reduce preterm lung injury.

优化肺扩张通气可调节早产羔羊通气引起的肺损伤。
导言:接近存活的早产儿通常需要机械通气(MV)来治疗呼吸窘迫综合征。尽管常用的是保肺通气技术,但机械通气时肺部的快速扩张会诱发肺损伤,这是导致支气管肺发育不良的一个危险因素。本研究探讨了优化肺扩张通气是否可行,以及是否能进一步减少肺损伤。因此,将优化肺扩张通气(OLEV)与传统的容量目标通气进行了比较:方法:20 只早产羔羊在妊娠 132 天后通过手术娩出。方法:20 只早产羔羊在妊娠 132 天后进行手术分娩,其中 9 只随机接受 24 小时的 OLEV 通气,7 只接受标准 MV 通气。四只未通气的动物作为对照组(NV)。实验结束后对肺部取样进行组织学分析:结果:使用 OLEV 通气是可行的,可显著提高平均通气压力(0.7-1.3 毫巴)。OLEV 和 MV 在氧合方面的暂时差异并未达到临床相关水平。与 NV 相比,一般通气往往会导致更高的肺损伤评分,但 OLEV 和 MV 之间并无差异。虽然与 NV 相比,两个通气组的促炎症肿瘤坏死因子-α 信使 RNA (mRNA) 水平都有所上升,但只有 MV 组动物的肺部 CD45 阳性细胞数量较多。相比之下,OLEV 组表面活性蛋白-B mRNA 的平均水平(标准偏差)显著降低,为 0.63(0.38),而 NV 组为 1.03(0.32)(p = .023,单因素方差分析):总之,在使用 OLEV 支持 24 小时后,肺部炎症略有减轻,这表明 OLEV 具有减轻早产儿肺损伤的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Pediatric Pulmonology
Pediatric Pulmonology 医学-呼吸系统
CiteScore
6.00
自引率
12.90%
发文量
468
审稿时长
3-8 weeks
期刊介绍: Pediatric Pulmonology (PPUL) is the foremost global journal studying the respiratory system in disease and in health as it develops from intrauterine life though adolescence to adulthood. Combining explicit and informative analysis of clinical as well as basic scientific research, PPUL provides a look at the many facets of respiratory system disorders in infants and children, ranging from pathological anatomy, developmental issues, and pathophysiology to infectious disease, asthma, cystic fibrosis, and airborne toxins. Focused attention is given to the reporting of diagnostic and therapeutic methods for neonates, preschool children, and adolescents, the enduring effects of childhood respiratory diseases, and newly described infectious diseases. PPUL concentrates on subject matters of crucial interest to specialists preparing for the Pediatric Subspecialty Examinations in the United States and other countries. With its attentive coverage and extensive clinical data, this journal is a principle source for pediatricians in practice and in training and a must have for all pediatric pulmonologists.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信