Department of Medicine and Women's Guild Lung Institute, Cedars-Sinai Medical Center, Los Angeles, California.
Department of Mechanical and Aerospace Engineering, Monash University, Melbourne, Victoria, Australia.
J Appl Physiol (1985). 2017 Sep 1;123(3):578-584. doi: 10.1152/japplphysiol.00903.2016. Epub 2017 Jun 8.
Increased dead space is an important prognostic marker in early acute respiratory distress syndrome (ARDS) that correlates with mortality. The cause of increased dead space in ARDS has largely been attributed to increased alveolar dead space due to ventilation/perfusion mismatching and shunt. We sought to determine whether anatomic dead space also increases in response to mechanical ventilation. Mice received intratracheal lipopolysaccharide (LPS) or saline and mechanical ventilation (MV). Four-dimensional computed tomography (4DCT) scans were performed at onset of MV and after 5 h of MV. Detailed measurements of airway volumes and lung tidal volumes were performed using image analysis software. The forced oscillation technique was used to obtain measures of airway resistance, tissue damping, and tissue elastance. The ratio of airway volumes to total tidal volume increased significantly in response to 5 h of mechanical ventilation, regardless of LPS exposure, and airways demonstrated significant variation in volumes over the respiratory cycle. These findings were associated with an increase in tissue elastance (decreased lung compliance) but without changes in tidal volumes. Airway volumes increased over time with exposure to mechanical ventilation without a concomitant increase in tidal volumes. These findings suggest that anatomic dead space fraction increases progressively with exposure to positive pressure ventilation and may represent a pathological process. We demonstrate that anatomic dead space ventilation increases significantly over time in mice in response to mechanical ventilation. The novel functional lung-imaging techniques applied here yield sensitive measures of airway volumes that may have wide applications.
死腔量增加是急性呼吸窘迫综合征(ARDS)早期的一个重要预后标志物,与死亡率相关。ARDS 中死腔量增加的原因主要归因于通气/血流不匹配和分流导致的肺泡死腔增加。我们试图确定机械通气是否也会导致解剖死腔增加。小鼠接受气管内脂多糖(LPS)或生理盐水和机械通气(MV)。在 MV 开始时和 MV 5 小时后进行四维计算机断层扫描(4DCT)扫描。使用图像分析软件对气道容积和肺潮气量进行详细测量。使用强迫振荡技术获得气道阻力、组织阻尼和组织弹性的测量值。无论 LPS 暴露与否,5 小时的机械通气都会导致气道容积与总潮气量的比值显著增加,气道在呼吸周期中表现出明显的容积变化。这些发现与组织弹性增加(肺顺应性降低)相关,但潮气量没有变化。气道容积随着机械通气的暴露而随时间增加,而潮气量没有增加。这些发现表明,解剖死腔分数随着正压通气的暴露而逐渐增加,可能代表一种病理过程。我们证明,在机械通气的情况下,小鼠的解剖死腔通气随着时间的推移显著增加。这里应用的新型功能肺部成像技术可提供敏感的气道容积测量值,可能具有广泛的应用。