MedPath

Postoperative Sore Throat: Interest of the Videolaryngoscope

Not Applicable
Completed
Conditions
Postoperative Pain
Tracheal Intubation Morbidity
Sore-throat
Anesthesia
Interventions
Procedure: tracheal intubation by Videolaryngoscope
Procedure: tracheal intubation by direct laryngoscope
Registration Number
NCT05614414
Lead Sponsor
Mongi Slim Hospital
Brief Summary

Postoperative sore throat is a complication of orotracheal intubation. The aim of our study was to assess the impact of videolaryngoscopy on postoperative sore throat during the first 24 hours following surgery.

This was a prospective, randomized study, over a period of 9 months. The investigators included 136 patients with non-difficult airway, classified ASA I to III and over 18 years old. The patients were randomized into 2 groups: the VL group including 70 patients intubated with direct laryngoscopy and the LD group including 66 patients intubated with videolaryngoscopy.

Detailed Description

The investigators monitored blood pressure, ECG, saturation in oxygen, capnograph, temperature and curarization. They also monitored cuff pressure using manometer.

The investigators pre-oxygenated the patients until the fractional expired oxygen was over 90%, then induced anaesthesia using either 2.5 to 3.5 mg/kg of propofol or 0.3 to 0.4 mg/kg of etomidate, then 1mg/kg of suxamethonium (in absence of contraindication). If modified crash induction was performed, the anaesthesiologist mentioned the opioid used.

The investigators performed laryngoscopy using either a Macintosh laryngoscope using a number 4 blade in LD group, or a McGrath video-laryngoscope with a number 4 blade in VL group and a stylet when needed. Women were intubated using number 7 tube and man using a 7.5 tube. They inflated the cuff with 7ml of air, and controlled pressure by manometer every 30 minutes in order to maintain it between 20 and 25 mmHg.

The investigators ventilated patients with assisted controlled mode using a 6ml/kg of ideal weight volume, a 6 mmHg PEEP, a 50% inspired fraction of oxygen and a respiratory rate guaranteeing an end-expiratory CO2 level between 35 and 40 mmHg. Then, they administrated 4 mg of Ondansetran in order to prevent postoperative nausea and vomiting (PONV).

The investigators maintained anaesthesia using either isoflurane or sevoflurane, 0.1 μg/kg of sufentanil and 0.05 mg/kg of atracurium.

Recruitment & Eligibility

Status
COMPLETED
Sex
Not specified
Target Recruitment
135
Inclusion Criteria
  • Patients aged over 18 years old;
  • Patients with ASA status 1, 2 or 3;
  • Patients who underwent surgery with general anaesthesia and intubation;
  • written consent.
Exclusion Criteria
  • Patients under corticosteroids;
  • Pregnant women;
  • Patient with at least two difficult intubation criteria or a limited mouth opening (under 2cm), difficult airway management history, upper airway tumour or cervical rachis trauma;
  • Patients who had an otorhinolaryngologic infection in the last month, an intubation or endoscopy of upper airway in the last 48 hours, vomiting in the last 24 hours, a gastric tube in the last 24 hours or throat symptoms prior to surgery;
  • Patients scheduled for a surgery implying a manipulation of upper airways;
  • Patient scheduled for a surgery > 2 hours.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
VL Grouptracheal intubation by VideolaryngoscopePatients who were intubated by videolaryngoscope.
LD Grouptracheal intubation by direct laryngoscopePatients who were intubated by direct laryngoscope
Primary Outcome Measures
NameTimeMethod
Postoperative sore throat6 hours after surgery

Postoperative sore throat assessed by verbal scale (from 0 to 10)

Secondary Outcome Measures
NameTimeMethod
Postoperative dysphagiaup to 24 hours after surgery

presence or no of dysphagia

Postoperative sore throatup to 24 hours after surgery.

Postoperative sore throat assessed by verbal scale (from 0 to 10)

Postoperative dysphoniaup to 24 hours after surgery

Presence or no of dysphonia

Trial Locations

Locations (1)

Mongi Slim University Hospital

🇹🇳

La Marsa, Tunis, Tunisia

© Copyright 2025. All Rights Reserved by MedPath