• Chest · Sep 2022

    Multicenter Study

    Factors Associated With Spontaneous Awakening Trial and Spontaneous Breathing Trial Performance in Critically Ill Adults: Analysis of a Multicenter, Nationwide, Cohort Study.

    • Michele C Balas, Alai Tan, Lorraine C Mion, Brenda Pun, Jin Jun, Audrey Brockman, Jinjian Mu, E Wesley Ely, and Eduard E Vasilevskis.
    • College of Nursing, University of Nebraska Medical Center, Omaha, NE. Electronic address: mibalas@unmc.edu.
    • Chest. 2022 Sep 1; 162 (3): 588602588-602.

    BackgroundBroad-scale adoption of spontaneous awakening trials (SATs) and spontaneous breathing trials (SBTs) into everyday practice has been slow, and uncertainty exists regarding what factors facilitate or impede their routine delivery.Research QuestionWhat patient, practice, and pharmacologic factors are associated with SAT and SBT performance and to what extent do they predict overall SAT/SBT performance?Study Design And MethodsThis secondary analysis used data collected from a national quality improvement collaborative composed of 68 diverse ICUs. Adults with critical illness adults who received mechanical ventilation and/or continuously infused sedative medications were included. We performed mixed-effects logistic regression modeling, created receiver operating characteristic curves, and calculated the area under the curve (AUC).ResultsIncluded in the SAT and SBT analysis were 4,847 and 4,938 patients, respectively. In multivariable models controlling for admitting patient characteristics, factors independently associated with higher odds of a next-day SAT and SBT included physical restraint use (adjusted odds ratio [AOR], 1.63; 95% CI, 1.42-1.87; AOR, 1.83; 95% CI, 1.60-2.09), documented target sedation level (AOR, 1.68; 95% CI, 1.41-2.01; AOR, 1.46; 95% CI, 1.24-1.72), more frequent level of arousal assessments (AOR, 1.22; 95% CI, 1.03-1.43; AOR, 1.32; 95% CI, 1.13-1.54), and dexmedetomidine administration (AOR, 1.23; 95% CI, 1.05-1.45; AOR, 1.52; 95% CI, 1.27-1.80). Factors independently associated with lower odds of a next-day SAT and SBT included deep sedation/coma (AOR, 0.69; 95% CI, 0.60-0.80; AOR, 0.33; 95% CI, 0.28-0.37) and benzodiazepine (AOR, 0.83; 95% CI, 0.72-0.95; AOR, 0.67; 95% CI, 0.59-0.77) or ketamine (AOR, 0.34; 95% CI, 0.16-0.71; AOR, 0.40; 95% CI, 0.18-0.88) administration. Models incorporating admitting, daily, and unit variations displayed moderate discriminant accuracy in predicting next-day SAT (AUC, 0.73) and SBT (AUC, 0.72) performance.InterpretationThere are a number of modifiable factors associated with SAT/SBT performance that are amenable to the development and testing of implementation interventions.Copyright © 2022 American College of Chest Physicians. Published by Elsevier Inc. All rights reserved.

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