MedPath

Post Operative Sore Throat and Dexamethasone

Phase 4
Completed
Conditions
Sore Throat
Pain
Interventions
Registration Number
NCT01052038
Lead Sponsor
Northwestern University
Brief Summary

Sore throat is a common postoperative complaint that can lead to morbidity and patient dissatisfaction . The incidence of sore throat has been reported to be between 6% and 90% even under optimal intubating conditions. There are several factors that have been shown to contribute to postoperative sore throat such as patient related factors, type of anesthesia and type of surgery.

Corticosteroids are also commonly used in the perioperative period to potentiate analgesics and as antiemetics. The preoperative administration of dexamethasone can decrease the incidence and severity of postoperative sore throat which is rated by patients as one of the most undesirable outcomes in the postoperative period.

Detailed Description

Sore throat is a common postoperative complaint that can lead to morbidity and patient dissatisfaction. The incidence of sore throat has been reported to be between 6% and 90% even under optimal intubating conditions. There are several factors that have been shown to contribute to postoperative sore throat such as patient related factors, type of anesthesia and type of surgery. It has been observed that gargle with azunol reduced the incidence of postoperative sore throat from 65% to 25 %. Similarly, a reduction in sore throat following tracheal intubation from 78% to 40 % has been reported after gargle with ketamine performed 5 minutes before induction of anesthesia. More recently, it was also demonstrated that preoperative gargle with licorice resulted in a 57 percent reduction of the absolute risk of sore throat after intubation. Although the gargling technique has been shown to be successful in decreasing the incidence of postoperative sore throat, it has a limited feasibility because the volumes administered could increase the chance of aspiration if ingested and it may be difficult to perform in sedated patients and in children.

Tracheal intubation is associated with an increase of polymorphonuclear cells in the tracheal tissue and plasma levels of interleukin 6, suggesting an inflammatory response to the presence of the endotracheal tube itself or to some aspect of the intubation process. Dexamethasone is widely prescribed for the treatment of a sore throat resulting from tracheal mechanical irritation due to its modulating effects of tissue edema and pain. Moreover, prophylactic dexamethasone has been shown to be effective in reducing the frequency of airway obstruction in patients at high risk for laryngeal edema following extubation. It decreases postoperative sore throat in patients requiring double-lumen tubes.

Dexamethasone has been shown to decrease postoperative sore throat in patients requiring hospital admission but it has not been evaluated in the ambulatory setting. Ambulatory patients usually need to return to work faster than patients who are admitted to the hospital. Their ability to tolerate fluids and food might help them to return to normal living. They also have smaller surgeries which might increased their perception to sore throat pain when compared to bigger, more painful procedures.

Possible side effects of corticosteroids such as retardation of wound healing, susceptibility to infection and gastrointestinal hemorrhage have not been noted with short term use (\<24 hours ) in surgical patients. Corticosteroids are also commonly used in the perioperative period to potentiate analgesics and as antiemetics.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
120
Inclusion Criteria
  • Female patients undergoing outpatient laparoscopic gynecologic surgery
  • ASA PS I and II
  • Age between 18 and 64 years
  • Fluent in English
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Exclusion Criteria
  • History of recent respiratory tract infection
  • Pregnancy, breastfeeding
  • Current treatment with analgesics
  • Current use of corticosteroids
  • Anticipated difficult intubation
  • Risk factors for post-operative aspiration
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Group 1 PlaceboPlacebo administrationNormal saline 100ml (placebo) administered as a intravenous infusion 30 minutes prior to surgery.
Group 2: Dexamethasone 0.05mg/kgDexamethasone 0.05mg/kr administrationDexamethasone 0.05 mg/kg administered in 100 ml of sterile saline solution prior to surgery
Group 3:Dexamethasone 0.1mg/kgDexamethasone 0.1mg/kgDexamethasone 0.1mg/kg administered in 100ml of sterile saline solution prior to surgery.
Primary Outcome Measures
NameTimeMethod
Subjects Assessment of Sore Throat Pain at 24 Hours24 hours

The reported score for sore throat on a 1 to 5 scale where 1 is a severe sore throat and 5 is no sore throat. This evaluation was made by investigator initiated phone conversation at 24 hours following surgery.

Secondary Outcome Measures
NameTimeMethod
Quality of Recovery at 24 Hours24 hours

The quality of recovery (QoR-40) questionnaire assess the subjects perceived quality of recovery following surgery. The tool assess pain, physical and psychological well being as well as ability to ability for self-care. Questions are scored on a 1 to 5 point scale with a higher value indication a better outcome. The scores or the individual questions are summed to obtain a total score. The minimum total score is 30 and the maximum is 200. The higher the score the better the recovery

Number of Subjects With Sore Throat at 3 Hours Post Surgery.3 hours.

Subjects were asked at 3 hours post surgery if they were experiencing a sore throat.

Opioid Consumption at 24 Hours24 hours

The cumulative use of an opioid analgesic pain medication taken during the first 24 hours for pain and discomfort. Data reported as equivalent dose of oral morphine.

Hoarseness at 24 Hours24 hours

Self assessment of the degree of hoarseness 24 hours after surgery and intratracheal intubation on a 1 to 1 Likert scale. 0 = no hoarseness and 3= hoarseness easily noted at time of interview.

Trial Locations

Locations (1)

Northwesten University

🇺🇸

Chicago, Illinois, United States

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