The aim of this study was to compare three different awake tracheal intubation technique
-fiberoptic bronchoscopy (ATI:FB), videolaryngoscopy (ATI:VL), and fiberoptic bronchoscopy via a supraglottic airway device (ATI:SAD)- in terms of success rates, intubation times, and complications. Additionally, the study aims to evaluate the reliability of the SAD-assisted ATI method and its potential to contribute to the literature.
Who can participate
Age range18 Years
SexALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Adult patients aged 18 and older
* Patients classified as ASA I-II according to the American Society of Anesthesiologists (ASA) classification
* Patients scheduled for elective surgery
* Patients expected to require difficult mask ventilation, difficult laryngoscopy, or difficult tracheal intubation; patients expected to have short apnea periods (Planjuan goiter); patients at risk of aspiration; patients expected to require difficult rescue techniques; and patients with a reported history of difficult intubation
* Patients scheduled for intubation using the awake tracheal intubation (ATI) method
* Individuals who have agreed to participate in the study by signing an informed consent form
Exclusion Criteria:
* Patients with a mouth opening \<1.5 cm
* Patients requiring emergency intubation or emergency surgery (situations where there is insufficient time to administer ATI)
* Patients who cannot cooperate (mental incapacity, impaired consciousness, inability to communicate, etc.)
* Patients with known allergies to lidocaine or other local/topical anesthetic agents used
* Pregnancy
* Patients with a history of severe cardiac arrhythmia or hemodynamic instability (due to increased risk during intubation)
* Patients who have previously undergone tracheostomy or whose airway is technically obstructed due to anatomical deformity
* Patients who refuse to participate in the study or who do not provide informed consent
What they're measuring
1
Success rate of chosen awake intubation method
Timeframe: Through study completion, an average of 2 year