Perioperative Dexamethasone Administration and Risk of Bleeding Following Tonsillectomy in Children A Randomized Controlled Trial

被引:52
作者
Gallagher, Thomas Q. [1 ]
Hill, Courtney [2 ]
Ojha, Shilpa [3 ]
Ference, Elisabeth [5 ]
Keamy, Donald G., Jr. [3 ]
Williams, Michael [3 ]
Hansen, Maynard [3 ]
Maurer, Rie [6 ]
Collins, Corey [4 ]
Setlur, Jennifer [3 ]
Capra, Gregory G. [7 ]
Brigger, Matthew T. [7 ]
Hartnick, Christopher J. [3 ]
机构
[1] USN, Dept Otolaryngol, Med Ctr Portsmouth, Portsmouth, VA USA
[2] Dartmouth Hitchcock Med Ctr, Dept Surg, Lebanon, NH 03766 USA
[3] Massachusetts Eye & Ear Infirm, Dept Otolaryngol, Boston, MA 02114 USA
[4] Massachusetts Eye & Ear Infirm, Dept Anesthesiol, Boston, MA 02114 USA
[5] Northwestern Univ, Dept Otolaryngol, Chicago, IL 60611 USA
[6] Brigham & Womens Hosp, Boston, MA 02115 USA
[7] USN, Dept Otolaryngol, San Diego Med Ctr, San Diego, CA 92152 USA
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2012年 / 308卷 / 12期
基金
美国国家卫生研究院;
关键词
HEMORRHAGE; ADENOTONSILLECTOMY; METAANALYSIS; ADENOIDECTOMY; COMPLICATIONS; MORBIDITY;
D O I
10.1001/2012.jama.11575
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:1221 / 1226
页数:6
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