Mechanical Ventilation Guided by Esophageal Pressure in Acute Lung Injury

被引:740
|
作者
Talmor, Daniel [1 ,6 ]
Sarge, Todd [1 ,6 ]
Malhotra, Atul [3 ,4 ,6 ]
O'Donnell, Carl R. [2 ,6 ]
Ritz, Ray [1 ]
Lisbon, Alan [1 ,6 ]
Novack, Victor [5 ]
Loring, Stephen H. [1 ,6 ]
机构
[1] Beth Israel Deaconess Med Ctr, Dept Anesthesia Crit Care & Pain Med, Boston, MA 02215 USA
[2] Beth Israel Deaconess Med Ctr, Div Pulm Crit Care & Sleep Med, Boston, MA 02215 USA
[3] Brigham & Womens Hosp, Div Pulm & Crit Care, Boston, MA 02115 USA
[4] Brigham & Womens Hosp, Div Sleep Med, Boston, MA 02115 USA
[5] Harvard Univ, Harvard Clin Res Inst, Boston, MA 02115 USA
[6] Harvard Univ, Sch Med, Boston, MA 02115 USA
来源
NEW ENGLAND JOURNAL OF MEDICINE | 2008年 / 359卷 / 20期
关键词
D O I
10.1056/NEJMoa0708638
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Survival of patients with acute lung injury or the acute respiratory distress syndrome (ARDS) has been improved by ventilation with small tidal volumes and the use of positive end-expiratory pressure (PEEP); however, the optimal level of PEEP has been difficult to determine. In this pilot study, we estimated transpulmonary pressure with the use of esophageal balloon catheters. We reasoned that the use of pleural-pressure measurements, despite the technical limitations to the accuracy of such measurements, would enable us to find a PEEP value that could maintain oxygenation while preventing lung injury due to repeated alveolar collapse or overdistention. Methods: We randomly assigned patients with acute lung injury or ARDS to undergo mechanical ventilation with PEEP adjusted according to measurements of esophageal pressure (the esophageal-pressure-guided group) or according to the Acute Respiratory Distress Syndrome Network standard-of-care recommendations (the control group). The primary end point was improvement in oxygenation. The secondary end points included respiratory-system compliance and patient outcomes. Results: The study reached its stopping criterion and was terminated after 61 patients had been enrolled. The ratio of the partial pressure of arterial oxygen to the fraction of inspired oxygen at 72 hours was 88 mm Hg higher in the esophageal-pressure-guided group than in the control group (95% confidence interval, 78.1 to 98.3; P=0.002). This effect was persistent over the entire follow-up time (at 24, 48, and 72 hours; P=0.001 by repeated-measures analysis of variance). Respiratory-system compliance was also significantly better at 24, 48, and 72 hours in the esophageal-pressure-guided group (P=0.01 by repeated-measures analysis of variance). Conclusions: As compared with the current standard of care, a ventilator strategy using esophageal pressures to estimate the transpulmonary pressure significantly improves oxygenation and compliance. Multicenter clinical trials are needed to determine whether this approach should be widely adopted. (ClinicalTrials.gov number, NCT00127491.).
引用
收藏
页码:2095 / 2104
页数:10
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