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Effects of Three Airway Instruments on the Incidence of Postoperative Sore Throat

F

Fu Jen Catholic University Hospital

Status

Completed

Conditions

Sore-throat

Treatments

Device: Direct Laryngoscope

Study type

Observational

Funder types

Other

Identifiers

NCT06515808
FJUH111171

Details and patient eligibility

About

Postoperative sore throat (POST) is a common complaint after general anesthesia. POST is defined by the presence of a self-reported foreign body sensation or a painful sensation in the throat after general anesthesia. This condition may affect recovery and patient satisfaction and is associated with many factors, including intubation tools. Previous studies have reported conflicting results on POST. This retrospective cohort study, with sample size of 10,382 patients, was conducted to confirm the hypothesis that the use of video laryngoscopy (VL) is associated with a lower incidence of POST compared with direct laryngoscopy (DL).

Full description

Background: Postoperative sore throat (POST) is a common complaint after general anesthesia. POST is defined by the presence of a self-reported foreign body sensation or a painful sensation in the throat after general anesthesia. This condition may affect recovery and patient satisfaction and is associated with many factors, including intubation tools. Previous studies have reported conflicting results on POST. This retrospective cohort study, with sample size of 10,382 patients, was conducted to confirm the hypothesis that the use of video laryngoscopy (VL) is associated with a lower incidence of POST compared with direct laryngoscopy (DL).

Methods: Data were extracted from a prospectively maintained quality improvement database. A total of 10,382 patients were included in the study. Statistical analysis was conducted for comparisons of demographic characteristics and to determine the effect of intubation tools on the incidence of POST.

Enrollment

10,382 patients

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients receiving inpatients surgery and general anesthesia with tracheal intubation

Exclusion criteria

  • Having difficult airway,

    • Anticipated difficult airway:

      1. Abnormal cervical spine movement or temporomandibular joint movement
      2. Airway-compromising masses such as tumors, cysts, or hematomas
      3. A Mallampati score greater than 3
      4. A thyromental distance of less than 6 cm
      5. A lesion below vocal cord
      6. A previously identified difficult airway
    • Unexpected difficult airway

      1. difficult mask ventilation
      2. difficult vocal cord visualization after multiple attempts of laryngoscopy
  • Receiving laryngeal surgery, such as laryngeal biopsy, laryngeal microsurgery, laryngoplasty or vocal cord surgery,

  • Not being extubated at the end of anesthesia,

  • Being pregnant,

  • Being under 20 years of age,

  • American Society of Anesthesiologists (ASA) physical status class greater than 3.

Trial design

10,382 participants in 3 patient groups

Direct Laryngoscope Group
Description:
Patients receiving tracheal intubation with direct laryngoscope
Treatment:
Device: Direct Laryngoscope
GlideScope Group
Description:
Patients receiving tracheal intubation with GlideScope
AirwayScope Group
Description:
Patients receiving tracheal intubation with AirwayScope

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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