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Short-term effects of combining upright and prone positions in patients with ARDS: a prospective randomized study

机译:合并直立和俯卧位对ARDS患者的近期影响:一项前瞻性随机研究

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IntroductionProne position is known to improve oxygenation in patients with acute lung injury (ALI) and the acute respiratory distress syndrome (ARDS). Supine upright (semirecumbent) position also exerts beneficial effects on gas exchange in this group of patients. We evaluated the effect of combining upright and prone position on oxygenation and respiratory mechanics in patients with ALI or ARDS in a prospective randomized cross-over study.MethodsAfter turning them prone from a supine position, we randomized the patients to a prone position or combined prone and upright position. After 2 hours, the position was changed to the other one for another 6 hours. The gas exchange and static compliance of the respiratory system, lungs, and chest wall were assessed in the supine position as well as every hour in the prone position.ResultsTwenty patients were enrolled in the study. The PaO2/FiO2 ratio improved significantly from the supine to the prone position and further significantly increased with additional upright position. Fourteen (70%) patients were classified as responders to the prone position, whereas 17 (85%) patients responded to the prone plus upright position compared with the supine position (P = n.s.). No statistically significant changes were found with respect to compliance.ConclusionsCombining the prone position with the upright position in patients with ALI or ARDS leads to further improvement of oxygenation.Trial registrationClinical Trials No. NCT00753129
机译:简介已知正确的姿势位置可以改善急性肺损伤(ALI)和急性呼吸窘迫综合征(ARDS)患者的氧合作用。仰卧位(半卧位)对这组患者的气体交换也具有有益作用。在一项前瞻性随机交叉研究中,我们评估了俯卧位和俯卧位组合对ALI或ARDS患者的充氧和呼吸力学的影响。方法将他们从仰卧位转为俯卧位后,我们将患者随机分为俯卧位或俯卧位和直立的姿势。 2小时后,该职位又换了另一个职位6个小时。在仰卧位以及俯卧位每小时评估呼吸系统,肺和胸壁的气体交换和静态顺应性。结果招募了20名患者。从仰卧位到俯卧位,PaO2 / FiO2的比例显着提高,而在其他直立位置,PaO2 / FiO2的比例也显着提高。与仰卧位相比,有十四名(70%)患者对俯卧位有反应,而17位(85%)患者对俯卧位和直立位有反应(P = n.s.)。在依从性方面未发现统计学上的显着变化。结论ALI或ARDS患者的俯卧位与直立位相结合可进一步改善氧合。临床注册临床试验编号NCT00753129

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