Dexamethasone and Risk of Nausea and Vomiting and Postoperative Bleeding After Tonsillectomy in Children A Randomized Trial

被引:135
作者
Czarnetzki, Christoph [1 ]
Elia, Nadia [1 ,4 ]
Lysakowski, Christopher [1 ]
Dumont, Lionel [1 ]
Landis, Basile N. [2 ]
Giger, Roland [2 ]
Dulguerov, Pavel [2 ,5 ]
Desmeules, Jules [3 ,5 ]
Tramer, Martin R. [1 ,5 ]
机构
[1] Univ Hosp Geneva, Div Anesthesiol, CH-1211 Geneva 14, Switzerland
[2] Univ Hosp Geneva, Div Otolaryngol Head & Neck Surg, CH-1211 Geneva 14, Switzerland
[3] Univ Hosp Geneva, Div Clin Pharmacol & Toxicol, CH-1211 Geneva 14, Switzerland
[4] Univ Geneva, Inst Social & Prevent Med, Geneva, Switzerland
[5] Univ Geneva, Fac Med, Geneva, Switzerland
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2008年 / 300卷 / 22期
关键词
D O I
10.1001/jama.2008.794
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Context Dexamethasone is widely used to prevent postoperative nausea and vomiting ( PONV) in pediatric tonsillectomy. Objective To assess whether dexamethasone dose- dependently reduces the risk of PONV at 24 hours after tonsillectomy. Design, Setting, and Patients Randomized placebo- controlled trial conducted among 215 children undergoing elective tonsillectomy at a major public teaching hospital in Switzerland from February 2005 to December 2007. Interventions Children were randomly assigned to receive dexamethasone ( 0.05, 0.15, or 0.5 mg/ kg) or placebo intravenously after induction of anesthesia. Acetaminophen-codeine and ibuprofen were given as postoperative analgesia. Follow- up continued until the 10th postoperative day. Main Outcome Measures The primary end point was prevention of PONV at 24 hours; secondary end points were decrease in the need for ibuprofen at 24 hours and evaluation of adverse effects. Results At 24 hours, 24 of 54 participants who received placebo ( 44%; 95% confidence interval [ CI], 31%- 59%) had experienced PONV compared with 20 of 53 ( 38%; 95% CI, 25%- 52%), 13 of 54 ( 24%; 95% CI, 13%- 38%), and 6 of 52 ( 12%; 95% CI, 4%- 23%) who received dexamethasone at 0.05, 0.15, and 0.5 mg/ kg, respectively ( P < .001 for linear trend). Children who received dexamethasone received significantly less ibuprofen. There were 26 postoperative bleeding episodes in 22 children. Two of 53 ( 4%; 95% CI, 0.5%- 13%) children who received placebo had bleeding compared with 6 of 53 ( 11%; 95% CI, 4%- 23%), 2 of 51 ( 4%; 95% CI, 0.5%-13%), and 12 of 50 ( 24%; 95% CI, 13%- 38%) who received dexamethasone at 0.05, 0.15, and 0.5 mg/ kg, respectively ( P=. 003). Dexamethasone, 0.5 mg/ kg, was associated with the highest bleeding risk ( adjusted relative risk, 6.80; 95% CI, 1.77- 16.5). Eight children had to undergo emergency reoperation because of bleeding, all of whom had received dexamethasone. The trial was stopped early for safety reasons. Conclusion In this study of children undergoing tonsillectomy, dexamethasone decreased the risk of PONV dose dependently but was associated with an increased risk of postoperative bleeding. Trial Registration clinicaltrials. gov Identifier: NCT00403806.
引用
收藏
页码:2621 / 2630
页数:10
相关论文
共 47 条
[1]
Steroids for post-tonsillectomy pain reduction: Meta-analysis of randomized controlled trials [J].
Afman, CE ;
Welge, JA ;
Steward, DL .
OTOLARYNGOLOGY-HEAD AND NECK SURGERY, 2006, 134 (02) :181-186
[2]
April MM, 1996, ARCH OTOLARYNGOL, V122, P117
[3]
*ASS PAED AN GREAT, 2008, GUID PREV POST OP VO
[4]
Prophylaxis of postoperative vomiting in children undergoing tonsillectomy: a systematic review and meta-analysis [J].
Bolton, C. M. ;
Myles, P. S. ;
Nolan, T. ;
Sterne, J. A. .
BRITISH JOURNAL OF ANAESTHESIA, 2006, 97 (05) :593-604
[5]
Brown P, 2004, LANCET, V364, P697
[6]
CATLIN FI, 1991, ARCH OTOLARYNGOL, V117, P649
[7]
Regulation of matrix metalloproteinases: An overview [J].
Chakraborti, S ;
Mandal, M ;
Das, S ;
Mandal, A ;
Chakraborti, T .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2003, 253 (1-2) :269-285
[8]
Establishing a standard definition for child overweight and obesity worldwide: international survey [J].
Cole, TJ ;
Bellizzi, MC ;
Flegal, KM ;
Dietz, WH .
BMJ-BRITISH MEDICAL JOURNAL, 2000, 320 (7244) :1240-1243
[9]
Collison P J, 2000, Ear Nose Throat J, V79, P640
[10]
Collison PJ, 2000, ENT-EAR NOSE THROAT, V79, P646