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Effects of pressure support ventilation on ventilator-induced lung injury in mild acute respiratory distress syndrome depend on level of positive end-expiratory pressure: A randomised animal study

机译:压力支持通气对轻度急性呼吸窘迫综合征的呼吸机引起的肺损伤依赖于阳性终端呼气压力水平:随机动物研究

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BACKGROUNDHarmful effects of spontaneous breathing have been shown in experimental severe acute respiratory distress syndrome (ARDS). However, in the clinical setting, spontaneous respiration has been indicated only in mild ARDS. To date, no study has compared the effects of spontaneous assisted breathing with those of fully controlled mechanical ventilation at different levels of positive end-expiratory pressure (PEEP) on lung injury in ARDS.OBJECTIVETo compare the effects of assisted pressure support ventilation (PSV) with pressure-controlled ventilation (PCV) on lung function, histology and biological markers at two different PEEP levels in mild ARDS in rats.DESIGNRandomised controlled experimental study.SETTINGBasic science laboratory.PARTICIPANTSThirty-five Wistar rats (weightSD, 31019)g received Escherichia coli lipopolysaccharide (LPS) intratracheally. After 24h, the animals were anaesthetised and randomly allocated to either PCV (n=14) or PSV (n=14) groups. Each group was further assigned to PEEP=2cmH(2)O or PEEP=5cmH(2)O. Tidal volume was kept constant (approximate to 6mlkg(-1)). Additional nonventilated animals (n=7) were used as a control for postmortem analysis.MAIN OUTCOME MEASURESVentilatory and mechanical parameters, arterial blood gases, diffuse alveolar damage score, epithelial integrity measured by E-cadherin tissue expression, and biological markers associated with inflammation (IL-6 and cytokine-induced neutrophil chemoattractant, CINC-1) and type II epithelial cell damage (surfactant protein-B) were evaluated.RESULTSIn both PCV and PSV, peak transpulmonary pressure was lower, whereas E-cadherin tissue expression, which is related to epithelial integrity, was higher at PEEP=5cmH(2)O than at PEEP=2cmH(2)O. In PSV, PEEP=5cmH(2)O compared with PEEP=2cmH(2)O was associated with significantly reduced diffuse alveolar damage score [median (interquartile range), 11 (8.5 to 13.5) vs. 23 (19 to 26), P=0.005] and expressions of IL-6 and CINC-1 (P=0.02 for both), whereas surfactant protein-B mRNA expression increased (P=0.03). These changes suggested less type II epithelial cell damage at a PEEP of 5cmH(2)O. Peak transpulmonary pressure correlated positively with IL-6 [Spearman's rho ()=0.62, P=0.0007] and CINC-1 expressions (=0.50, P=0.01) and negatively with E-cadherin expression (=-0.67, P=0.0002).CONCLUSIONDuring PSV, PEEP of 5cmH(2)O, but not a PEEP of 2cmH(2)O, reduced lung damage and inflammatory markers while maintaining epithelial cell integrity.
机译:自发性呼吸的背景已显示在实验严重急性呼吸窘迫综合征(ARDS)中显示出来。然而,在临床环境中,仅在轻度ARDS中表明了自发呼吸。迄今为止,没有研究与在ARDS中肺损伤的不同水平的阳性末期呼气压力(PEEP)的完全控制的机械通气的效果进行了比较了自发辅助呼吸的影响.Bobjectiveto比较辅助压力支持通气(PSV)的影响在大鼠轻度ARDS中,在肺功能(PCV)对肺功能(PCV)对肺功能,组织学和生物标志物,在大鼠中的两种不同窥视水平。诱导基本科学实验室。ParttingAntshiRty-Five Wistar Rats(重量,31019)G接受大肠杆菌脂多糖(LPS)内肿瘤内。 24小时后,将动物麻醉并随机分配给PCV(n = 14)或pSV(n = 14)组。每组进一步分配给PEEP = 2cmH(2)O或PEEP = 5cmH(2)o。潮气量保持恒定(近似为6mlkg(-1))。额外的非透明的动物(n = 7)被用作后期分析的对照。鉴定结果,动脉血液,弥漫性肺泡损伤评分,由e-cadherin组织表达测量的上皮完整性,以及与炎症相关的生物标志物(评估IL-6和细胞因子诱导的嗜中性粒细胞化学反对剂,CINC-1)和II型上皮细胞损伤(表面活性剂蛋白-B)。培养PCV和PSV,峰值二核压力较低,而E-Cadherin组织表达,即与上皮完整性有关,在PEEP = 5cmH(2)o时较高,而不是PEEP = 2cmH(2)o。在PSV中,与PEEP = 2cmH(2)o与PEEP = 5cmH(2)o与显着减少的漫射肺泡损伤评分[中位数(四分位数范围),11(8.5至13.5)与23(19至26)相关联。 p = 0.005]和IL-6和CINC-1的表达(两者为0.22),而表面活性剂蛋白-B mRNA表达增加(p = 0.03)。这些变化表明,在5cmH(2)o的PEEP下较少的II型上皮细胞损伤。峰值经跨玻璃压力与IL-6 [Spearman的rhO()= 0.62,p = 0.0007]和CINC-1表达(= 0.50,p = 0.01)和对e-cadherin表达(= -0.67,p = 0.0002)负相关(= 0.50,p = 0.01) .CLUSESMENDUREDPERUCED,PEEP为5cmH(2)o,但不是2cmH(2)o的PEEP,降低肺部损伤和炎症标志物,同时保持上皮细胞完整性。

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    Univ Fed Rio de Janeiro Lab Pulm Invest Carlos Chagas Filho Biophys Inst Rio De Janeiro Brazil;

    Univ Fed Rio de Janeiro Lab Pulm Invest Carlos Chagas Filho Biophys Inst Rio De Janeiro Brazil;

    Univ Fed Rio de Janeiro Lab Pulm Invest Carlos Chagas Filho Biophys Inst Rio De Janeiro Brazil;

    Univ Fed Rio de Janeiro Lab Pulm Invest Carlos Chagas Filho Biophys Inst Rio De Janeiro Brazil;

    Univ Fed Rio de Janeiro Lab Pulm Invest Carlos Chagas Filho Biophys Inst Rio De Janeiro Brazil;

    Univ Fed Rio de Janeiro Lab Pulm Invest Carlos Chagas Filho Biophys Inst Rio De Janeiro Brazil;

    Prof Fernando Figueira Inst Comprehens Med Grad Program Maternal &

    Child Hlth Recife PE Brazil;

    Prof Fernando Figueira Inst Comprehens Med Grad Program Maternal &

    Child Hlth Recife PE Brazil;

    Univ Fed Rio de Janeiro Fac Med Expt Surg Lab Rio De Janeiro Brazil;

    Univ Sao Paulo Sch Med Dept Pathol Sao Paulo Brazil;

    Univ Hosp Carl Gustav Carus Dept Anesthesiol &

    Intens Care Therapy Pulm Engn Grp Dresden Germany;

    Univ Hosp Carl Gustav Carus Dept Anesthesiol &

    Intens Care Therapy Pulm Engn Grp Dresden Germany;

    Univ Genoa Dept Surg Sci &

    Integrated Diagnost IRCCS AOU San Martino IST Genoa Italy;

    Univ Fed Rio de Janeiro Lab Pulm Invest Carlos Chagas Filho Biophys Inst Rio De Janeiro Brazil;

    Univ Fed Rio de Janeiro Lab Pulm Invest Carlos Chagas Filho Biophys Inst Rio De Janeiro Brazil;

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