Current Practices and Safety of Medication Use During Pediatric Rapid Sequence Intubation

Author:

Bisesi Sarah A.1,Stauber Sierra D.2,Hutchinson David J.3,Acquisto Nicole M.4

Affiliation:

1. Department of Pharmacy (SAB), University of Rochester Medical Center, Rochester, NY;

2. Department of Pharmacy (SDS), University of Rochester Medical Center, Rochester, NY;

3. Department of Pharmacy Practice and Education (DJH), St. John Fisher University, Wegmans School of Pharmacy, Rochester, NY;

4. Departments of Pharmacy and Emergency Medicine (NMA), University of Rochester Medical Center, Rochester, NY

Abstract

OBJECTIVES This study aimed to characterize medication-related practices during and immediately ­following rapid sequence intubation (RSI) in pediatric care units across the United States and to evaluate adverse drug events. METHODS This was a multicenter, observational study of medication practices surrounding intubation in pediatric and neonatal intensive care unit (NICU) and emergency department patients across the United States. RESULTS A total of 172 patients from 13 geographically diverse institutions were included. Overall, 24%, 69%, and 50% received preinduction, induction, and neuromuscular blockade, respectively. Induction and neuromuscular blocking agent (NMBA) use was low in NICU patients (52% and 23%, respectively), whereas nearly all patients intubated outside of the NICU received both (98% and 95%, respectively). NICU patients who received RSI medications were older and weighed more. Despite infrequent use of atropine (21%), only 3 patients developed bradycardia after RSI. Of the 119 patients who received an induction agent, fentanyl (67%) and midazolam (34%) were administered most frequently. Hypotension and hypertension occurred in 23% and 24% of patients, respectively, but were not associated with a single induction agent. Etomidate use was low and not associated with development of adrenal insufficiency. Rocuronium was the most used NMBA (78%). Succinylcholine use was low (11%) and administered despite hyperkalemia in 2 patients. Postintubation sedation and analgesia were not used or inadequate based on timing of initiation in many patients who received a non-depolarizing NMBA. CONCLUSIONS Medication practices surrounding pediatric RSI vary across the United States and may be influenced by patient location, age, and weight.

Publisher

Pediatric Pharmacy Advocacy Group

Reference19 articles.

1. Current practices and safety of medication use during rapid sequence intubation: a multicenter study evaluating practices across the United States;Groth;J Crit Care,2018

2. Rapid sequence induction and intubation: current controversies;El-Orbany;Anesth Analg,2010

3. Challenges and advances in intubation: rapid sequence intubation;Mace;Emerg Med Clin N Am,2008

4. Controversies in rapid sequence intubation in children;Zelicof-Paul;Curr Opin Pediatr,2005

5. Single induction dose of etomidate versus other induction agents for endotracheal intubation in critically ill patients;Bruder;Cochrane Database Syst Rev,2015

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