TY - JOUR
T1 - Effect of pressure support vs T-piece ventilation strategies during spontaneous breathing trials on successful extubation among patients receiving mechanical ventilation
T2 - A randomized clinical trial
AU - Subirà, Carles
AU - Hernández, Gonzalo
AU - Vázquez, Antònia
AU - Rodríguez-Garciá, Raquel
AU - González-Castro, Alejandro
AU - Garciá, Carolina
AU - Rubio, Olga
AU - Ventura, Lara
AU - López, Alexandra
AU - De La Torre, Maria Carmen
AU - Keough, Elena
AU - Arauzo, Vanesa
AU - Hermosa, Cecilia
AU - Sánchez, Carmen
AU - Tizón, Ana
AU - Tenza, Eva
AU - Laborda, César
AU - Cabañes, Sara
AU - Lacueva, Victoria
AU - Del Mar Fernández, Maria
AU - Arnau, Anna
AU - Fernández, Rafael
N1 - Publisher Copyright:
© 2019 American Medical Association. All rights reserved.
PY - 2019/6/11
Y1 - 2019/6/11
N2 - 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.
AB - 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.
UR - https://www.scopus.com/pages/publications/85066928016
U2 - 10.1001/jama.2019.7234
DO - 10.1001/jama.2019.7234
M3 - Article
C2 - 31184740
AN - SCOPUS:85066928016
SN - 0098-7484
VL - 321
SP - 2175
EP - 2182
JO - JAMA - Journal of the American Medical Association
JF - JAMA - Journal of the American Medical Association
IS - 22
ER -