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Spontaneous-Breathing Trials with Pressure-Support Ventilation or a T-Piece

医学 四分位间距 自主呼吸试验 通风(建筑) 麻醉 置信区间 压力支持通气 机械通风 随机对照试验 呼吸衰竭 外科 内科学 机械工程 工程类
作者
Arnaud W. Thille,Arnaud Gacouin,Rémi Coudroy,Stéphan Ehrmann,Jean‐Pierre Quenot,Mai-Anh Nay,Christophe Guitton,Damien Contou,Guylaine Labro,Jean Reignier,Gaël Pradel,G. Béduneau,Laurence Dangers,Clément Saccheri,Gwénaël Prat,Guillaume Lacave,Nicholas Sédillot,Nicolas Terzi,Béatrice La Combe,Jean‐Paul Mira
出处
期刊:The New England Journal of Medicine [Massachusetts Medical Society]
卷期号:387 (20): 1843-1854 被引量:96
标识
DOI:10.1056/nejmoa2209041
摘要

Spontaneous-breathing trials can be performed with the use of either pressure-support ventilation (PSV) or a T-piece. Whether PSV trials may result in a shorter time to tracheal extubation than T-piece trials, without resulting in a higher risk of reintubation, among patients who have a high risk of extubation failure is unknown.In this multicenter, open-label trial, we randomly assigned patients who had a high risk of extubation failure (i.e., were >65 years of age or had an underlying chronic cardiac or respiratory disease) to undergo spontaneous-breathing trials performed with the use of either PSV (with a pressure-support level of 8 cm of water and no positive end-expiratory pressure) or a T-piece. The primary outcome was the total time without exposure to invasive ventilation (reported as the number of ventilator-free days) at day 28 after the initial spontaneous-breathing trial. Secondary outcomes included extubation within 24 hours and extubation within 7 days after the initial spontaneous-breathing trial, as well as reintubation within 7 days after extubation.A total of 969 patients (484 in the PSV group and 485 in the T-piece group) were included in the analysis. At day 28, the median number of ventilator-free days was 27 (interquartile range, 24 to 27) in the PSV group and 27 (interquartile range, 23 to 27) in the T-piece group (difference, 0 days; 95% confidence interval [CI], -0.5 to 1; P = 0.31). Extubation was performed within 24 hours in 376 patients (77.7%) in the PSV group and in 350 patients (72.2%) in the T-piece group (difference, 5.5 percentage points; 95% CI, 0.01 to 10.9), and extubation was performed within 7 days in 473 patients (97.7%) and 458 patients (94.4%), respectively (difference, 3.3 percentage points; 95% CI, 0.8 to 5.9). Reintubation was performed in 72 of 481 patients (14.9%) in the PSV group and in 65 of 477 patients (13.6%) in the T-piece group (difference, 1.3 percentage points; 95% CI, -3.1 to 5.8). Cardiac or respiratory arrest was a reason for reintubation in 9 patients (3 in the PSV group and 6 in the T-piece group).Among patients who had a high risk of extubation failure, spontaneous-breathing trials performed with PSV did not result in significantly more ventilator-free days at day 28 than spontaneous-breathing trials performed with a T-piece. (Supported by the French Ministry of Health; TIP-EX ClinicalTrials.gov number, NCT04227639.).
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