Jessica Kent1, Emily Austin2,3,4, Brodie Nolan2,3,5. 1. Division of Emergency Medicine, Department of Medicine, University of Toronto, Toronto, ON, Canada. jekent@nosm.ca. 2. Division of Emergency Medicine, Department of Medicine, University of Toronto, Toronto, ON, Canada. 3. Department of Emergency Medicine, St. Michael's Hospital, Toronto, ON, Canada. 4. Ontario Poison Centre, Toronto, ON, Canada. 5. Li Ka Shing Knowledge Institute, St. Michael's Hospital, Toronto, ON, Canada.
Full Citation: Barbic D, Andolfatto G, Grunau B, Scheuermeyer F, Macewan B, Qian H, Wong H, Barbic S, Honer W. Rapid Agitation Control with Ketamine in the Emergency Department: A Blinded, Randomized Controlled Trial. Ann. Emerg. Med.. 2021Abstract Link:
https://www.annemergmed.com/article/S0196-0644(21)00433-9/fulltextArticle Type: Randomized Control TrialRatings:
Methods—4/5, Usefulness—4/5
Introduction
Background
Severely agitated emergency department (ED) patients require rapid stabilization to avoid endangering themselves and staff. Administration of intramuscular agents with rapid onset is preferred to maximize safety.
Objective
To compare time to sedation between intramuscular ketamine or a combination of intramuscular haloperidol and midazolam in ED patients with agitation.
Structured methods
Design
A single-center randomized controlled trial (RCT).
Setting
St. Paul’s Hospital, an urban Canadian emergency department.
Subjects
Patients aged 19–60 years of age with severe psychomotor agitation measured by a Richmond Agitation Score (RASS) of 3 or greater.
Intervention
Ketamine 5 mg/kg intramuscular.
Comparison
Haloperidol 5 mg and Midazolam 5 mg intramuscular.
Outcomes
The primary outcome of this study was time from medication administration (in minutes) to adequate sedation, defined as Richmond Agitation Score (RASS) of − 1 or less. Secondary outcomes of this study included the need for rescue medication and the occurrence of prespecified adverse events.
Main results
Of 308 patients screened, 80 were enrolled and randomized equally into the two study arms. The majority of patients enrolled were male (68%), with a median age of 35 years [IQR 29.0–41.5]. A greater proportion of patients receiving ketamine were male (85%) with a higher RASS score of 4 + (64.1%). The primary outcome of median time to sedation was 14.7 min for midazolam and haloperidol versus 5.8 min for ketamine (difference 8.8 min [95% confidence interval (CI) 3.0 to 14.5]). Adjusted Cox proportional model analysis favored the ketamine arm (hazard ratio 2.43, 95% CI 1.43 to 4.12). As a secondary outcome, 5 (12.5%) patients who received ketamine and 2 (5.0%) patients who received midazolam and haloperidol experienced serious adverse events (difference 7.5% [95% CI − 4.8 to 19.8%]). There was no difference in proportion of patients requiring rescue medications between groups. The trial was halted early due to COVID-19 restrictions.
Appraisal
Strengths
Prospective RCT adherent to CONSORT guidelinesWell-defined clinical question with practical designClear inclusion and exclusion criteria which did not exclude those with schizophrenia/psychosisTreatment allocation concealed from staff, investigators, research assistants and patientsUse of RASS as an objective measure for both inclusion into the study and target for sedationPractical comparison using appropriate dosages of haloperidol and midazolamUse of standardized criteria for prespecified adverse events
Limitations
Small sample size which did not reach targetSingle-centre trial at a hospital where staff were comfortable managing severely agitated patients which may not reflect all EDsPossible recruitment bias—study hours between 8 am and midnightPotential for un-blinding—ketamine split into multiple vials based on patient weight, whereas midazolam and haloperidol given in a single vialFrequency of harms commonly encountered when treating agitated patients not reported (ex, needle stick injury)Impact on disposition/length of stay not reported
Context
Benzodiazepines, antipsychotics, or a combination of both have typically been recommended for chemical sedation of agitated ED patients [1]. While effective, these medications are slow to work and have unwanted side effects including respiratory depression [1]. Given ketamine’s rapid onset and favorable side effect profile, the American College of Emergency Physicians has recommended its use for the rapid sedation of severely agitated patients whilst recognizing the need for further high-quality studies to establish safety/efficacy [2, 3]. Local experts in Toronto suggest using intramuscular ketamine in very agitated patients who are at imminent risk of harm to themselves or staff and require rapid sedation to facilitate a safe and thorough assessment.
Bottom line
In this single-centre randomized control trial, ketamine provided a significantly shorter time to sedation in comparison to haloperidol and midazolam without compromising safety in the severely agitated ED patient. These results need to be taken in the context of a study that did not reach target sample size and were under-powered to detect adverse events. Despite the limitations, ketamine appears to be a viable option for initial stabilization of the severely agitated ED patient if administered in a highly monitored setting.
Authors: Devorah J Nazarian; Joshua S Broder; Molly E W Thiessen; Michael P Wilson; Leslie S Zun; Michael D Brown Journal: Ann Emerg Med Date: 2017-04 Impact factor: 5.721