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Effect of Pressure Support vs T-Piece Ventilation Strategies During Spontaneous Breathing Trials on Successful Extubation Among Patients Receiving Mechanical Ventilation

医学 通风(建筑) 自主呼吸试验 麻醉 压力支持通气 随机对照试验 机械通风 断奶 重症监护室 重症监护 最大吸气压力 重症监护医学 外科 呼吸系统 潮气量 内科学 工程类 机械工程
作者
Carlés Subirá,Gonzalo Hernández,Antònia Vázquez,Raquel Rodríguez-García,A. González-Castro,Carolina García,Olga Rubio,Lara Ventura,Alexandra López,Maria-Carmen de la Torre,Elena Keough,Vanesa Arauzo,Cecilia Hermosa,Carmen Sánchez‐Torres,Ana Isabel Tizón,Eva María Olivares Tenza,César Laborda,Sara Cabañes,Victoria Lacueva,Mar Fernández‐Gutiérrez
出处
期刊:JAMA [American Medical Association]
卷期号:321 (22): 2175-2175 被引量:210
标识
DOI:10.1001/jama.2019.7234
摘要

Importance

Daily spontaneous breathing trials (SBTs) are the best approach to determine whether patients are ready for disconnection from mechanical ventilation, but mode and duration of SBT remain controversial.

Objective

To evaluate the effect of an SBT consisting of 30 minutes of pressure support ventilation (an approach that is less demanding for patients) vs an SBT consisting of 2 hours of T-piece ventilation (an approach that is more demanding for patients) on rates of successful extubation.

Design, Setting, and Participants

Randomized clinical trial conducted from January 2016 to April 2017 among 1153 adults deemed ready for weaning after at least 24 hours of mechanical ventilation at 18 intensive care units in Spain. Follow-up ended in July 2017.

Interventions

Patients were randomized to undergo a 2-hour T-piece SBT (n = 578) or a 30-minute SBT with 8-cm H2O pressure support ventilation (n = 557).

Main Outcome and Measures

The primary outcome was successful extubation (remaining free of mechanical ventilation 72 hours after first SBT). Secondary outcomes were reintubation among patients extubated after SBT; intensive care unit and hospital lengths of stay; and hospital and 90-day mortality.

Results

Among 1153 patients who were randomized (mean age, 62.2 [SD, 15.7] years; 428 [37.1%] women), 1018 (88.3%) completed the trial. Successful extubation occurred in 473 patients (82.3%) in the pressure support ventilation group and 428 patients (74.0%) in the T-piece group (difference, 8.2%; 95% CI, 3.4%-13.0%;P = .001). Among secondary outcomes, for the pressure support ventilation group vs the T-piece group, respectively, reintubation was 11.1% vs 11.9% (difference, −0.8%; 95% CI, −4.8% to 3.1%;P = .63), median intensive care unit length of stay was 9 days vs 10 days (mean difference, −0.3 days; 95% CI, −1.7 to 1.1 days;P = .69), median hospital length of stay was 24 days vs 24 days (mean difference, 1.3 days; 95% CI, −2.2 to 4.9 days;P = .45), hospital mortality was 10.4% vs 14.9% (difference, −4.4%; 95% CI, −8.3% to −0.6%;P = .02), and 90-day mortality was 13.2% vs 17.3% (difference, −4.1% [95% CI, −8.2% to 0.01%;P = .04]; hazard ratio, 0.74 [95% CI, 0.55-0.99]).

Conclusions and Relevance

Among patients receiving mechanical ventilation, a spontaneous breathing trial consisting of 30 minutes of pressure support ventilation, compared with 2 hours of T-piece ventilation, led to significantly higher rates of successful extubation. These findings support the use of a shorter, less demanding ventilation strategy for spontaneous breathing trials.

Trial Registration

ClinicalTrials.gov Identifier:NCT02620358
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