Comparative evaluation of nebulized versus intravenous dexmedetomidine on intubating conditions during awake fiberoptic nasotracheal intubation

• Published in: Journal of clinical anesthesia 2024-08, Vol.95, p.111461, Article 111461
• Main Authors: Bhalotra, Anju Romina, Arya, Mona, Singh, Rahil, Dhiman, Shweta
• Format: Article
• Language: English
• Subjects: Administration, Inhalation; Administration, Intravenous; Adult; Airway management; Anesthesia; Awake intubation; Bronchoscopy; Cardiac arrhythmia; Clinical outcomes; Cooperation; Dexmedetomidine - administration & dosage; Dexmedetomidine - adverse effects; Double-Blind Method; Elective surgery; Female; Fiber Optic Technology; General anesthesia; Hemodynamics; Humans; Hypnotics and Sedatives - administration & dosage; Hypnotics and Sedatives - adverse effects; Hypotension; Intubation; Intubation response; Intubation, Intratracheal - adverse effects; Intubation, Intratracheal - methods; Male; Middle Aged; Nebulized Dexmedetomidine; Nebulizers and Vaporizers; Patient Satisfaction; Postoperative period; Premedication; Side effects; Surgery; Wakefulness - drug effects; Young Adult
• ISSN: 0952-8180; 1873-4529; 1873-4529
• DOI: 10.1016/j.jclinane.2024.111461

There is a search for an ideal agent to facilitate awake fiberoptic intubation (AFOI). Dexmedetomidine is a selective α2 agonist which can be administered through intravenous, intramuscular, buccal, intranasal & inhalational routes. It provides good intubation conditions without oxygen desaturation but may cause hypotension and bradycardia when administered intravenously. Hence, alternative routes of administering dexmedetomidine which may improve its safety profile are worth exploring. In this randomised, controlled, double-blind trial, 46 ASA I/II adult participants scheduled for elective ENT surgery were randomly allocated to Group ND (Nebulised Dexmedetomidine) (n = 23) to receive nebulisation with dexmedetomidine 1μg.kg−1 and Group ID (Intravenous Dexmedetomidine) (n = 23) to receive intravenous dexmedetomidine 1μg.kg−1 before AFOI. All the patients received injection midazolam 1 mg i.v. as premedication before anaesthesia was initiated. The primary outcome was the cough score. The secondary outcomes were the RSS, SAYGO boluses, post-intubation score, hemodynamic parameters, recall of the procedure, patient satisfaction score and any side effects. The cough score was significantly lower in nebulized group (2.43 ± 0.992 vs 3.52 ± 1.082) with p = 0.001. RSS(3.30 ± 0.926 vs 4.22 ± 1.126; p = 0.004), number of SAYGO boluses required (2.74 ± 0.864 vs 3.57 ± 1.161; p = 0.009) & the post intubation score (1.48 ± 0.593 vs 2.17 ± 0.778; p = 0.001) were also significantly lower in nebulized group. Nebulisation with dexmedetomidine results in desirable degree of sedation and better tolerance of the procedure with adequate attenuation of the haemodynamic responses to intubation. •There is a search for an ideal agent to facilitate awake fiberoptic intubation (AFOI).•I.V. Dexmedetomidine provides good intubation conditions without oxygen desaturation but may cause hypotension and bradycardia.•Nebulised dexmedetomidine provided desirable sedation and better tolerance of the procedure without haemodynamic side effects.