Biological markers of lung injury before and after the institution of positive pressure ventilation in patients with acute lung injury

被引:34
作者
Cepkova, Magda
Brady, Sandra
Sapru, Anil
Matthay, Michael A.
Church, Gwynne
机构
[1] Univ Calif San Francisco, Cardiovasc Res Inst, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Anesthesia, San Francisco, CA 94143 USA
来源
CRITICAL CARE | 2006年 / 10卷 / 05期
关键词
D O I
10.1186/cc5037
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background Several biological markers of lung injury are predictors of morbidity and mortality in patients with acute lung injury (ALI). The low tidal volume lung-protective ventilation strategy is associated with a significant decrease in plasma biomarker levels compared to the high tidal volume ventilation strategy. The primary objective of this study was to test whether the institution of lung-protective positive pressure ventilation in spontaneously ventilating patients with ALI exacerbates preexisting lung injury by using measurements of biomarkers of lung injury before and after intubation. Materials and methods A prospective observational cohort study was conducted in the intensive care unit of a tertiary care university hospital. Twenty-five intubated, mechanically ventilated patients with ALI were enrolled. Physiologic data and serum samples were collected within 6 hours before intubation and at two different time points within the first 24 hours after intubation to measure the concentration of interleukin (IL)-6, IL-8, intercellular adhesion molecule 1 (ICAM-1), and von Willebrand factor (vWF). The differences in biomarker levels before and after intubation were analysed using repeated measures analysis of variance and a paired t test with correction for multiple comparisons. Results Before endotracheal intubation, all of the biological markers (IL-8, IL-6, ICAM-1, and vWF) were elevated in the spontaneously breathing patients with ALI. After intubation and the institution of positive pressure ventilation ( tidal volume 7 to 8 ml/kg per ideal body weight), none of the biological markers was significantly increased at either an early ( 3 +/- 2 hours) or later ( 21 +/- 5 hours) time point. However, the levels of IL-8 were significantly decreased at the later time point ( 21 +/- 5 hours) after intubation. During the 24-hour period after intubation, the PaO2/FiO(2) ( partial pressure of arterial oxygen/fraction of the inspired oxygen) ratio significantly increased and the plateau airway pressure significantly decreased. Conclusion Levels of IL-8, IL-6, vWF, and ICAM-1 are elevated in spontaneously ventilating patients with ALI prior to endotracheal intubation. The institution of a lung-protective ventilation strategy with positive pressure ventilation does not further increase the levels of biological markers of lung injury. The results suggest that the institution of a lung-protective positive pressure ventilation strategy does not worsen the preexisting lung injury in most patients with ALI.
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