The Effect of The Use of a Videolaryngoscope and/or Stylet on Intubation Time in Obese Patients
- Conditions
- Intubation Time
- Interventions
- Procedure: Endotracheal Tube + Video-laryngoscopeProcedure: Endotracheal Tube AloneProcedure: Endotracheal Tube+ StyletProcedure: Endotracheal tube + stylet with Video-laryngoscope
- Registration Number
- NCT05026671
- Lead Sponsor
- Karaman Training and Research Hospital
- Brief Summary
Although many researchers would agree that obesity per se is not a risk factor for difficult intubation, there are many well known obesity-related challenges in airway management including difficulty with mask ventilation, more frequent and rapid oxygen desaturation, increased oxygen consumption, and increased sensitivity to the respiratory depressant effects of anesthetic and analgesic drugs. Hence, in these conditions, rapid and nontraumatic intubation gain higher interest. There is controversy about using videoaryngoscopy (VL) in obese patients in these difficult situations. The primary aim of this study is to compare, in terms of intubation time, VL,VL plus stylet and direct-laryngoscopy(DL) plus stylet combination with DL alone in obese patients.
- Detailed Description
Patients who will be scheduled for surgeries requiring endotracheal intubation, with a body mass index (BMI) more than 30 kg/m2, will be included to this study. During preanesthetic visit (performed by an anesthesiologist not involved in this study) history of difficult intubation, measurement of common predictive indices for difficult intubation (BMI, thyromental distance, neck circumference, Mallampati grade, interincisal \[or intergingival\] distances), and evaluation of status of dentition and neck movement will be noted.
In the operating room, all patients will be connected to standard monitoring devices. Anesthesia induction will be carried out according to our hospital obese patient anesthesia management protocol. Then, after induction of anesthesia, the patients will be intubated one of four pre-defined protocols that will be determined via randomization during a preanesthetic visit by a person who is unfamiliar with the research protocol.
Primary hypothesis of this study is; using a video-laryngoscope plus stylet will reduce the time required to achieve successful tracheal intubation in obese patients.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 120
- Patients with a documented body mass index (BMI) of ≥ 30.
- Patients scheduled to undergo inpatient surgery procedures under general anesthesia.
- Willingness and ability to sign an informed consent document 18 - 80 years of age
- Patients who are deemed to be such a significant of an airway risk that they necessitate awake fiberoptic intubation
- Patients with a history of facial abnormalities, oral-pharyngeal cancer, or reconstructive surgery
- Emergency surgeries
- Pregnancy
- Any other conditions or use of any medication which may interfere with the conduct of the study.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Group VL Endotracheal Tube + Video-laryngoscope The Experimental consists of intubating the trachea with an endotracheal tube + Video-laryngoscope Group DL Endotracheal Tube Alone The control group consists of intubating the trachea with an endotracheal tube alone (without stylet). Group DLS Endotracheal Tube+ Stylet The Experimental group consists of intubating the trachea with an endotracheal tube + stylet. Group VLS Endotracheal tube + stylet with Video-laryngoscope The Experimental consists of intubating the trachea with an endotracheal tube + stylet + Video-laryngoscope
- Primary Outcome Measures
Name Time Method Intubation Time Using a Stop Watch Up to 3 minutes The timing measurements will begin once the laryngoscope blade will be placed in the patient's mouth and ended when an end-tidal CO2 tracing will be detected.
- Secondary Outcome Measures
Name Time Method Glottis View Using the Cormack Lehane Score Up to 1 minute Cormack Lehane score classification
Grade 1: Most of the glottis is visible Grade 2: At best almost half of the glottis is seen, at worst only the posterior tip of the arytenoids is seen Grade 3: Only the epiglottis is visible Grade 4: No laryngeal structures are visibleNumber of intubation attempts Up to postinduction 120 second An intubation attempt will be defined as the insertion of the laryngoscope blade into the mouth of the patient, regardless of whether an attempt will be made to insert a tracheal tube. More than 5 attempts or 120 s will be regarded as a failure of intubation.
Saturation Before induction to 3 min after intubation Before induction, after induction, after intubation, after intubation at 1st minute, 2nd minute, and 3rd minute
Complications related to intubation postoperative 4th hour A postoperative follow-up assessment will be performed approximately 4 hr after surgery by a co-investigator blinded to the intubation device to evaluate the presence and severity of sore throat, any changes in voice, trauma to the lip, tongue, gum, or teeth.
Incidence of severe complications following intubation During intubation to 3 min after intubation Hypoxia, collapse, cardiac arrest, death.
Heart Rate Before induction to 3 min after intubation Before induction, after induction, after intubation, after intubation at 1st minute, 2nd minute, and 3rd minute
Mean Arterial Pressure: Before induction to 3 min after intubation Before induction, after induction, after intubation, after intubation at 1st minute, 2nd minute, and 3rd minute
Glottis View Using the POGO Score Up to 1 minute the POGO score evaluate the glottic view during tracheal intubation using a classification of 1/2/3/4 and a score of 0% to 100%, respectively. The POGO score denote visualization of the entire glottic opening from the anterior commissure to the posterior cartilages, and a score of 0% denotes inability to visualize any part of the glottic opening.
Ease of Intubation Up to 1 minute Subjective evaluation of the anesthesiologist, rated as (1) very easy, (2) easy, (3) moderate, (4) difficult, and (5) impossible.
Trial Locations
- Locations (1)
Karaman Training and Research Hospital
🇹🇷Karaman, Turkey