Frequency of Screening and SBT Technique Trial

Summary

Participation Requirements

Description

Identifying the optimal time when patients are ready to be weaned from invasive ventilation is challenging and often arbitrary. To identify weaning candidates, current guidelines recommend that clinicians use a combination of subjective clinical assessments and objective measurements. However, clini...

Identifying the optimal time when patients are ready to be weaned from invasive ventilation is challenging and often arbitrary. To identify weaning candidates, current guidelines recommend that clinicians use a combination of subjective clinical assessments and objective measurements. However, clinician's subjective assessments of weaning readiness underestimate the probability that patients can be successfully liberated from mechanical ventilation. Even the most objective measurement, the respiratory frequency to tidal volume ratio or rapid shallow breathing index (f/VT), has only limited value [Likelihood ratio + 1.58 (1.30 -1.90)] in predicting successful extubation after a trial of spontaneous breathing trial (SBT). More than two decades of research support the use of specific strategies to limit the duration of invasive ventilation including the (i) use of multidisciplinary screening protocols to identify SBT candidates, (ii) conduct of SBTs in patients who meet screening criteria, and (iii) use of specific modes and techniques Pressure Support (PS) and once daily SBTs [e.g., PS or T-piece (no support)] to discontinue support in patients who fail an initial SBT and require weaning. Compared to usual care, earlier trials have shown that protocolized weaning, led by allied health care providers (RTs, nurses) reduced weaning time. A systematic review and meta-analysis of 11 trials involving 1,971 critically ill patients, conducted by one investigative member of the study team (KB), demonstrated that screening protocols reduce the total duration of mechanical ventilation, the time spent weaning and ICU length of stay. Only 1 trial (n=385) compared twice daily screening led by RTs and bedside nurses to usual care (requiring a physician order to conduct an SBT) and found a significantly shorter duration of ventilation and a trend toward a lower ventilator-associated pneumonia (VAP) rate in the twice daily screening group. The investigator's prior work demonstrates that once daily screening is the current standard of care nationally and internationally. Further, no trial has compared two of the most frequently used SBT techniques internationally [PS and T-piece]. Consequently, little is known about how frequently patients should be screened and what technique should be used to conduct SBTs in Canadian ICUs today. The FAST trial will address these important gaps in knowledge. The proposed study is novel in seeking to identify the optimal screening and SBT strategies to minimize patients' exposure to invasive ventilation and the complications associated with it. It will evaluate how weaning strategies are delivered to critically ill adults and determine whether alternative delivery strategies may improve patient outcomes. Only one weaning trial has been conducted in Canada previously by members of the investigative team (KB, MM). Establishing the role for more frequent screening is appealing to ICU clinicians (intensivists, RTs, nurses, physiotherapists) because it is a sensible and low-risk intervention that represents a cost-effective use of current resources. Moreover, this simple intervention holds promise as a strategy that could change clinical practice, enhance the care delivered to critically ill adults, and improve patient outcomes. In the FAST Trial,eligible patients will be randomized to a screening frequency (once vs. at least twice daily) and an SBT technique (PS vs. T-piece). The investigators propose to evaluate the feasibility of conducting an open-label, multicentre, factorial design trial involving 100 critically ill adults which compares screening frequency and SBT technique in 12 Canadian ICUs. In the pilot trial, the investigators will (i) evaluate their ability to recruit the desired population, (ii) assess clinician adherence to the screening and SBT protocols, (iii) identify potential confounders, (iv) characterize trial participants based on weaning difficulty, and (iv) obtain preliminary estimates of the effect of the alternative screening and SBT strategies on important outcomes. In the pilot trial, the investigative team will also assess 'current practices' with regard to sedation, analgesia, and delirium management, as well as, timing of mobilization prior to screening assessments to identify practices that may bias duration of ventilation and require protocolization in the future, planned large scale weaning trial. All participating adult ICUs currently titrate sedation use to either the Sedation-Agitation Scale (SAS) or Richmond Agitation Sedation Scale (RASS), have dedicated RT personnel present 24 hours per day/7 days per week and have either full time, part time, or consulting Physiotherapists. The investigators will determine if the proposed multicentre screening randomized control trial (RCT) is: A. Feasible, specifically, can the investigative team: Recruit critically ill adults breathing spontaneously on Pressure Support (PS) or proportional assist ventilation (PAV), or triggering breaths on volume or pressure Assist Control (AC), volume or pressure Synchronized Intermittent Mandatory Ventilation (SIMV) ± PS, Pressure Regulated Volume Control (PRVC) or Airway Pressure Release Ventilation (APRV) into a trial comparing 'once daily' to 'at least twice daily' screening to identify weaning candidates, Comply with 'once daily' and 'at least twice daily' screening assessment protocols with minimal contamination in 'once daily' arm, Comply with PS and T-piece SBT protocols with minimal contamination in either arm, Quantify potential co-interventions (sedation, analgesia and delirium management and timing of mobilization) that may lead to performance bias and may require protocolization in the future, planned, large scale weaning trial, Identify barriers (clinician and institutional) to recruitment, Classify trial participants as those requiring (i) simple, (ii) difficult or (iii) prolonged weaning using established definitions, Obtain preliminary estimates of the impact of the alternative screening ('once daily' vs. 'at least twice daily') and SBT techniques (PS vs. T-piece) on important outcomes [e.g., time to first SBT and first successful SBT, time to first extubation and successful extubation, total duration of mechanical ventilation, ICU and hospital length of stay, ICU and hospital mortality, the use of noninvasive ventilation (NIV) after extubation B. Safe, with regard to the proportion of patients experiencing weaning related complications (self-extubation, reintubation, tracheostomy) in both screening and SBT strategies. Information obtained from the pilot trial will inform the design of the planned large scale trial evaluating the time to first successful SBT completion (SBT outcome) and the time to first successful extubation (weaning and extubation outcome). In this manner, the investigators will assess the feasibility of conducting a multicentre, multinational RCT addressing this important research question.

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