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Face-to-face Intubation in Morbidly Obese

M

Medical University of Lodz

Status

Completed

Conditions

Intubation;Difficult
Obesity, Morbid

Treatments

Device: AirTraq videolaryngoscope

Study type

Interventional

Funder types

Other

Identifiers

NCT04959149
RNN/62/20/KE

Details and patient eligibility

About

Introduction : In a typical endotracheal intubation, the patient is in the supine position, with the anesthetist standing behind his head and with adequate access to the head and neck of the patient. However, there are several situations, where traditional intubation is very difficult or even impossible. In immobilised trauma victims, with limited access to the head, suspected cervical spine injury or in sitting positioned patient an intubation performed by a person standing in front of a patient might be the only chance of airway management. Moreover, in case of general anesthesia in bariatric patients, face-to-face (inverse) method is increasingly being considered due to upper body elevation position, recommended in this group of patients.

This was a parallel randomised controlled trial in patients scheduled for planned sleeve gastrectomy in Barlicki University Hospital, Lodz, Poland. Randomization and allocation to trial group were carried out by drawing envelopes by independent observer before a procedure. Randomized and recruited participants were 76 adults (typical intubation n= 36, face-to-face intubation n=40). Main outcome was a time of intubation using Airtraq video laryngoscope measured by independent assistant.

Full description

Aim : The aim of the study is to evaluate the effectiveness and safety of face-to-face intubation in airway management.

Methods : Patients admitted to hospital for elective sleeve gastrectomy procedure will be included in the study protocol. Before induction of anaesthesia the draw of the method will be held. The choice of method of intubation (inverse or typical) will be random.

  1. All patients will be positioned with the elevation of the upper body about 30 degrees. The standard anesthesia monitoring involves electrocardiogram, pulsoxymetry, non-invasive blood pressure and end-tidal carbon dioxide.
  2. Patients will be pre-oxygenated for 5 min. with 100% oxygen using facemask.
  3. The induction of general anesthesia will be performed by the intravenous administration of 1-2 µg.kg-1 of fentanyl and 2-2,5 mg.kg-1 propofol.
  4. After mask ventilation possibility is confirmed, rocuronium in a dose of 0,6 mg.kg-1 will be given.
  5. After obtaining an optimal muscle relaxation (90 s.) patient will be intubated. In face-to-face method an anesthetist is standing in front of a patient. In typical intubation an anesthetist is standing behind the patient's head.
  6. In case of prolonged face-to-face intubation (>120 s) or 2 unsuccessful attempts, patients are supposed to be intubated in a traditional way with the same video laryngoscope.
  7. General anesthesia will be continued with desflurane and a mixture of the oxygen and air, volume-controlled ventilation parameters will be adjusted to age and ideal body weight.

Enrollment

76 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. BMI > 40 kg.m-2
  2. Patients qualified for planned sleeve gastrectomy.
  3. Patients of I and II class of ASA scale.
  4. Patients without history of difficult intubation.

Exclusion criteria

  1. Patients in life threatening states.
  2. Patients of III, IV, V and VI class of ASA scale.
  3. History of difficult intubation.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

76 participants in 2 patient groups

face-to-face intubation
Experimental group
Description:
intubation approach from front of the patient
Treatment:
Device: AirTraq videolaryngoscope
standard position intubation
Active Comparator group
Description:
intubation approach from behind the head of the patient
Treatment:
Device: AirTraq videolaryngoscope

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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