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ARDS 患者个体化 PEEP 设置:一项随机对照初步研究。

Individualized PEEP setting in subjects with ARDS: a randomized controlled pilot study.

机构信息

Intensive Care Unit, Foundation for Biomedical Research, Hospital Universitario Príncipe de Asturias, Alcalá de Henares, Madrid, Spain.

出版信息

Respir Care. 2013 Sep;58(9):1416-23. doi: 10.4187/respcare.02068. Epub 2013 Jan 29.

DOI:10.4187/respcare.02068
PMID:23362167
Abstract

BACKGROUND

Low-tidal-volume ventilation may be associated with repetitive opening and closing of terminal airways. The use of PEEP is intended to keep the alveoli open. No method of adjusting the optimal PEEP has shown to be superior or to improve clinical outcomes. We conducted a pilot study to evaluate the effect of setting an individualized level of PEEP at the highest compliance on oxygenation, multiple-organ-dysfunction, and survival in subjects with ARDS.

METHODS

Subjects with ARDS ventilated with low tidal volumes and limitation of airway pressure to 30 cm H2O were randomized to either a compliance-guided PEEP group or an FIO2-guided group.

RESULTS

Of the 159 patients with ARDS admitted during the study period, 70 met the inclusion criteria. Subjects in the compliance-guided group showed nonsignificant improvements in PaO2/FIO2 during the first 14 days, and in 28-day mortality (20.6% vs. 38.9%, P = .12). Multiple-organ-dysfunction-free days (median 6 vs 20.5 d, P = .02), respiratory-failure-free days (median 7.5 vs 14.5 d, P = .03), and hemodynamic-failure-free days (median 16 vs 22 d, P = .04) at 28 days were significantly lower in subjects with compliance-guided setting of PEEP.

CONCLUSIONS

In ARDS subjects, protective mechanical ventilation with PEEP application according to the highest compliance was associated with less organ dysfunction and a strong nonsignificant trend toward lower mortality. ClinicalTrials.gov Number NCT01119872.

摘要

背景

低潮气量通气可能与终末气道的反复开闭有关。使用 PEEP 的目的是保持肺泡开放。没有一种调整最佳 PEEP 的方法被证明是优越的或能改善临床结果。我们进行了一项初步研究,以评估在 ARDS 患者中设定最佳 PEEP 水平以达到最高顺应性对氧合、多器官功能障碍和生存的影响。

方法

接受低潮气量通气和气道压力限制在 30cmH2O 的 ARDS 患者被随机分为顺应性指导的 PEEP 组或 FIO2 指导的组。

结果

在研究期间,159 例 ARDS 患者中,有 70 例符合纳入标准。顺应性指导组患者在最初 14 天内 PaO2/FIO2 无显著改善,28 天死亡率(20.6%比 38.9%,P=0.12)也无显著改善。无多器官功能障碍天数(中位数 6 天比 20.5 天,P=0.02)、无呼吸衰竭天数(中位数 7.5 天比 14.5 天,P=0.03)和无血流动力学衰竭天数(中位数 16 天比 22 天,P=0.04)在 28 天时明显较低。

结论

在 ARDS 患者中,根据最高顺应性应用 PEEP 的保护性机械通气与较少的器官功能障碍和死亡率有较弱的非显著趋势相关。ClinicalTrials.gov 编号 NCT01119872。

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