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Perioperative dexamethasone administration and risk of bleeding following tonsillectomy in children: a randomized
Thomas Q Gallagher1, Courtney Hill, Shilpa Ojha
1Department of Otolaryngology, Naval Medical Center Portsmouth, Portsmouth, Virginia, USA.
Insights
Dexamethasone did not significantly increase severe bleeding after pediatric tonsillectomy. However, it may lead to more subjective bleeding events, warranting careful consideration for its use.
Area of Science:
- Pediatric surgery
- Anesthesiology
- Otolaryngology
Background:
- Corticosteroids are frequently used in pediatric tonsillectomy to manage nausea and vomiting.
- Concerns exist regarding their potential to elevate risks of perioperative and postoperative hemorrhage.
Purpose of the Study:
- To evaluate the impact of dexamethasone on post-tonsillectomy bleeding in children.
- To test the hypothesis that dexamethasone does not increase bleeding events by more than 5% compared to placebo.
Main Methods:
- A multicenter, randomized, double-blind, placebo-controlled trial involving 314 children aged 3-18 years.
- Participants received either a single perioperative dose of dexamethasone or a placebo.
- Bleeding severity was assessed using a 14-day postoperative follow-up and a standardized bleeding scale.
Main Results:
- The study included 157 children in each group.
- Level I bleeding (subjective) occurred in 7.0% of the dexamethasone group versus 4.5% in the placebo group.
- Clinically significant bleeding (Level II and III) rates were low and not significantly increased by dexamethasone.
Conclusions:
- Perioperative dexamethasone in pediatric tonsillectomy is not linked to excessive clinically significant bleeding (Level II/III).
- The noninferiority threshold for subjective bleeding (Level I) was crossed, suggesting a potential increase in minor bleeding events.
Context:
Corticosteroids are commonly given to children undergoing tonsillectomy to reduce postoperative nausea and vomiting; however, they might increase the risk of perioperative and postoperative hemorrhage.
Objective:
To determine the effect of dexamethasone on bleeding following tonsillectomy in children.
Design, Setting, And Patients:
A multicenter, prospective, randomized, double-blind, placebo-controlled study at 2 tertiary medical centers of 314 children aged 3 to 18 years undergoing tonsillectomy without a history of bleeding disorder or recent corticosteroid medication use and conducted between July 15, 2010, and December 20, 2011, with 14-day follow-up. We tested the hypothesis that dexamethasone would not result in 5% more bleeding events than placebo using a noninferiority statistical design.
Intervention:
A single perioperative dose of dexamethasone (0.5 mg/kg; maximum dose, 20 mg), with an equivalent volume of 0.9% saline administered to the placebo group.
Main Outcome Measures:
Rate and severity of posttonsillectomy hemorrhage in the 14-day postoperative period using a bleeding severity scale (level I, self-reported or parent-reported postoperative bleeding; level II, required inpatient admission for postoperative bleeding; or level III, required reoperation to control postoperative bleeding).
Results:
One hundred fifty-seven children (median [interquartile range] age, 6 [4-8] years) were randomized into each study group, with 17 patients (10.8%) in the dexamethasone group and 13 patients (8.2%) in the placebo group reporting bleeding events. In an intention-to-treat analysis, the rates of level I bleeding were 7.0% (n = 11) in the dexamethasone group and 4.5% (n = 7) in the placebo group (difference, 2.6%; upper limit 97.5% CI, 7.7%; P for noninferiority = .17); rates of level II bleeding were 1.9% (n = 3) and 3.2% (n = 5), respectively (difference, -1.3%; upper limit 97.5% CI, 2.2%; P for noninferiority < .001); and rates of level III bleeding were 1.9% (n = 3) and 0.6% (n = 1), respectively (difference, 1.3%; upper limit 97.5% CI, 3.8%; P for noninferiority = .002).
Conclusions:
Perioperative dexamethasone administered during pediatric tonsillectomy was not associated with excessive, clinically significant level II or III bleeding events based on not having crossed the noninferior threshold of 5%. Increased subjective (level I) bleeding events caused by dexamethasone could not be excluded because the noninferiority threshold was crossed.
Trial Registration:
clinicaltrials.gov Identifier: NCT01415583.
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