Primary aim of this study is to identify independent factors associated with difficult videolaryngoscopic intubation in patients undergoing oral and maxillofacial (OMF) or ear, nose and throat (ENT) surgery. Furthermore, this study intends to assess the diagnostic value of preoperative flexible nasal videoendoscopy to predict difficult videolaryngoscopic intubation in these patients.
Difficult endotracheal intubation is a major reason for anesthesia related adverse events. Videolaryngoscopy has become an important part of the anesthesiological standard of care for difficult airway management in the past decades. Still, medical preconditions, as well as procedural and technical factors related with difficult videolaryngoscopy have not been systematically investigated, and a standardized comprehensive classification system for the severity of videolaryngoscopic intubation has yet to be specified. The primary objective of this study is to identify independent factors associated with difficult videolaryngoscopic intubation in patients undergoing ENT or OMF surgery. Patients with conditions of the ENT and OMF spectrum have a predisposition for difficult airway management and are at high risk for adverse events during endotracheal intubation. However, current recommendations for preoperative screening for difficult intubation rarely consider space consuming lesions of the laryngopharyngeal region. Comprehensive data identifying the predictive value of preoperative flexible nasal videoendoscopy as a diagnostic measure to anticipate difficult airway management still lack. Thus, secondary aim of this study is to evaluate the diagnostic value and clinical significance of preoperative flexible nasal videoendoscopy to predict difficult videolaryngoscopic intubation in these patients. Study design: The investigators conduct a prospective observational study, which includes 400 patients with predicted difficult airway and confirmed indication for flexible nasal videoendoscopy and videolaryngoscopic intubation undergoing ENT or OMF surgery. Procedural and surgical data as well as medical preconditions will be assessed systematically. The handling anesthetist and two independent observers will be surveyed (structured questionnaire) in order to assess procedural and technical factors related with videolaryngoscopic intubation.
Study Type
OBSERVATIONAL
Enrollment
400
no intervention
University Medical Center Hamburg-Eppendorf
Hamburg, Germany
Difficult videolaryngoscopic intubation
Questionnaire
Time frame: 30 minutes after endotracheal intubation
Successful first intubation attempt
Observation during airway management
Time frame: 30 minutes after endotracheal intubation
Overall success
Observation during airway management
Time frame: 30 minutes after endotracheal intubation
Unsuccessful videolaryngoscopy
Observation during airway management
Time frame: 30 minutes after endotracheal intubation
Severity of videolaryngoscopic intubation
Numeral rating scale
Time frame: 30 minutes after endotracheal intubation
Specific recommendations of the handling anesthetist
Questionnaire
Time frame: 30 minutes after endotracheal intubation
Time to successful intubation
Observation during airway management
Time frame: 30 minutes after endotracheal intubation
Number of laryngoscopy and intubation attempts
Observation during airway management
Time frame: 30 minutes after endotracheal intubation
Lowest oxygen saturation during airway management
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Observation during airway management
Time frame: 30 minutes after endotracheal intubation
Initial end-tidal carbon dioxide level after successful intubation
Observation during airway management
Time frame: 30 minutes after endotracheal intubation
Observed complications during or after induction of general anesthesia
Questionnaire
Time frame: 30 minutes after endotracheal intubation
Length of hospital stay
Follow-up
Time frame: Until hospital discharge up to 3 months after surgery
All cause in-hospital mortality
Follow-up
Time frame: Until hospital discharge up to 3 months after surgery