Comparison of Standard rapi̇d Sequential Intubation Protocol With Rocuronium in Emergency Department

This study is a prospective, observational and randomized study conducted between 15.07.2021 and 01.12.2021 in Ankara City Hospital Emergency Medicine Clinic, which is a third-level emergency department with approximately 450,000 patient admissions per year. Patients who applied to the emergency department and needed rapid sequential intubation were included in our study. Randomization was done according to the order of arrival of the cases. The demographic characteristics of the patients included in the study and the presence of diabetes mellitus were recorded. Routine rapid sequential intubation was performed in the standard group. In the priming group, 10% of the rocuronium dose was administered approximately 3 minutes before the induction agent. Intubation time, amount of drug used, vital signs before and after intubation, and end tidal carbon dioxide level to confirm intubation were recorded.

Inclusion criteria

• Be over the age of 18
• Need for advanced airway
• To give consent or consent to participate in the study consent of relatives of those who are unable to give

Exclusion criteria

• Have an indication of a crush (rescue) airway
• Have one of the difficult airway predictor Look, Evaluate, Obstruction, Neck mobility criteria
• maxillofacial anomaly or trauma
• detected during laryngoscopy with a cormack-lehane score of 3 and 4 patients
• Those who have inconveniences in applying ketamine to the clinic of the patient
• with a rocuronium or ketamine allergy