Wean Earlier and Automatically with New Technology (the WEAN Study) A Multicenter, Pilot Randomized Controlled Trial

被引:42
|
作者
Burns, Karen E. A. [1 ,2 ,3 ]
Meade, Maureen O. [4 ]
Lessard, Martin R. [5 ,6 ]
Hand, Lori [7 ]
Zhou, Qi [4 ]
Keenan, Sean P. [8 ]
Lellouche, Francois [5 ,9 ]
机构
[1] Univ Toronto, Interdept Div Crit Care Med, Toronto, ON, Canada
[2] St Michaels Hosp, Keenan Res Ctr, Toronto, ON M5B 1W8, Canada
[3] St Michaels Hosp, Li Ka Shing Knowledge Inst, Toronto, ON M5B 1W8, Canada
[4] McMaster Univ, Dept Clin Epidemiol & Biostat, Hamilton, ON, Canada
[5] Univ Laval, Div Adult Crit Care Med, Quebec City, PQ, Canada
[6] Hop Enfants Jesus, CHU Quebec, Populat Hlth Practice Changing Res Unit Trauma Em, Res Ctr, Quebec City, PQ, Canada
[7] Hamilton Gen Hosp, Hamilton Hlth Sci Ctr, Hamilton, ON, Canada
[8] Royal Columbian Hosp, Div Crit Care, New Westminster, BC, Canada
[9] Inst Univ Cardiol & Pneumol Quebec, Ctr Rech, Quebec City, PQ, Canada
基金
加拿大健康研究院;
关键词
positive pressure respiration; weaning; randomized trial; outcomes; VENTILATOR-ASSOCIATED PNEUMONIA; POSITIVE-PRESSURE VENTILATION; MECHANICAL VENTILATION; MOISTURE EXCHANGERS; RESPIRATORY-FAILURE; SUPPORT VENTILATION; T-TUBE; PROTOCOL; EXTUBATION; DURATION;
D O I
10.1164/rccm.201206-1026OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Rationale: Automated weaning has not been compared with a paper-based weaning protocol in North America. Objectives: We conducted a pilot randomized trial comparing automated weaning with protocolized weaning in critically ill adults to evaluate clinician compliance and acceptance of the weaning and sedation protocols, recruitment, and impact on outcomes. Methods: From August 2007 to October 2009, we enrolled critically ill adults requiring more than 24 hours of mechanical ventilation and at least partial reversal of the condition precipitating respiratory failure at nine Canadian intensive care units. We randomized patients who tolerated at least 30 minutes of pressure support and either failed or were not yet ready to undergo a spontaneous breathing trial to automated or protocolized weaning. Both groups used pressure support, included spontaneous breathing trials, used a common positive end-expiratory pressure-FIO2 chart, sedation protocol, and criteria for extubation, reintubation, and noninvasive ventilation. Measurements and Main Results: We recruited 92 patients (49 automated, 43 protocolized) over 26 months. Adherence to assigned weaning protocols and extreme sedation scale scores fell within pre-specified thresholds. Combined physician-respiratory therapist and nurse acceptance scores of the study weaning and sedation protocols, respectively, were not significantly different. Automated weaning patients had significantly shorter median times to first successful spontaneous breathing trial (1.0 vs. 4.0 d; P < 0.0001), extubation (3.0 vs. 4.0 d; P = 0.02), and successful extubation (4.0 vs. 5.0 d; P = 0.01), and underwent fewer tracheostomies and episodes of protracted ventilation. Conclusions: Compared with a standardized protocol, automated weaning was associated with promising outcomes that warrant further investigation. Minor protocol modifications may increase compliance, facilitate recruitment, and enhance feasibility.
引用
收藏
页码:1203 / 1211
页数:9
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