2015 HSC Section 1 Book of Articles

DEXAMETHASONE AND BLEEDING RISK AFTER TONSILLECTOMY

enotonsillectomy patients for preventing vomiting, re- ducing pain, shortening time to first liquid intake, or the incidence of voice change. Anesth Analg . 2007; 104(5):1052-1058. 5. Papangelou L. Steroid therapy in tonsillectomy. Laryngoscope . 1972;82(2):297-301. 6. Goldman AC, Govindaraj S, Rosenfeld RM. Ameta- analysis of dexamethasone use with tonsillectomy. Oto- laryngol Head Neck Surg . 2000;123(6):682-686. 7. Steward DL, Welge JA, Myer CM. Do steroids re- duce morbidity of tonsillectomy? meta-analysis of ran- domized trials. Laryngoscope . 2001;111(10):1712- 1718. 8. Baugh RF, Archer SM, Mitchell RB, et al; Ameri- can Academy of Otolaryngology-Head and Neck Sur- gery Foundation. Clinical practice guideline: tonsillec- tomy in children. Otolaryngol Head Neck Surg . 2011; 144(1)(suppl):S1-S30. 9. Czarnetzki C, Elia N, Lysakowski C, et al. Dexa- methasone and risk of nausea and vomiting and post- operative bleeding after tonsillectomy in children: a randomized trial. JAMA . 2008;300(22):2621-2630. 10. Blakley BW. Post-tonsillectomy bleeding: how much is toomuch? Otolaryngol Head Neck Surg . 2009; 140(3):288-290. 11. Collison PJ, Mettler B. Factors associated with post- tonsillectomy hemorrhage. Ear Nose Throat J . 2000; 79(8):640-642. 12. Brigger MT, CunninghamMJ, Hartnick CJ. Dexa- methasone administration and postoperative bleed- ing risk in children undergoing tonsillectomy. ArchOto- laryngol Head Neck Surg . 2010;136(8):766-772. 13. Ross AT, Kazahaya K, Tom LW. Revisiting out- patient tonsillectomy in young children. Otolaryngol Head Neck Surg . 2003;128(3):326-331. 14. Carmody D, Vamadevan T, Cooper SM. Post ton- sillectomy haemorrhage. J Laryngol Otol . 1982; 96(7):635-638. 15. Capper JWR, Randall C. Post-operative haemor- rhage in tonsillectomy and adenoidectomy in children. J Laryngol Otol . 1984;98(4):363-365. 16. Handler SD, Miller L, Richmond KH, Baranak CC. Post-tonsillectomy hemorrhage: incidence, preven- tion and management. Laryngoscope . 1986;96 (11):1243-1247. 17. Kristensen S, Tvetera˚s K. Post-tonsillectomy haem- orrhage: a retrospective study of 1150 operations. Clin Otolaryngol Allied Sci . 1984;9(6):347-350. 18. Windfuhr JP, Chen YS. Incidence of post- tonsillectomy hemorrhage in children and adults: a study of 4,848 patients. Ear Nose Throat J . 2002; 81(9):626-628. 19. Gallagher TQ, Wilcox L, McGuire E, Derkay CS. Analyzing factors associated with major complica- tions after adenotonsillectomy in 4776 patients: com- paring three tonsillectomy techniques. Otolaryngol Head Neck Surg . 2010;142(6):886-892. 20. Derkay CS, DarrowDH, Welch C, Sinacori JT. Post- tonsillectomy morbidity and quality of life in pediat- ric patients with obstructive tonsils and adenoid: mi- crodebrider vs electrocautery. Otolaryngol Head Neck Surg . 2006;134(1):114-120. 21. Steward DL, Welge JA, Myer CM. Steroids for im- proving recovery following tonsillectomy in children. Cochrane Database Syst Rev . 2003;(1):CD003997. 22. Macassey EA, Baguley C, Dawes P, Gray A. 15- year audit of post-tonsillectomy haemorrhage at Dune- din Hospital. ANZ J Surg . 2007;77(7):579-582. 23. Gunter JB, Willging JP, Myer CM III. Dexameth- asone and postoperative bleeding after tonsillec- tomy in children. JAMA . 2009;301(17):1764-1765. 24. Shargorodsky J, Hartnick CJ, Lee GS. Dexameth- asone and postoperative bleeding after tonsillec- tomy and adenotonsillectomy in children: a meta- analysis of prospective studies. Laryngoscope . 2012; 122(5):1158-1164. 25. Conley SF, EllisonMD. Avoidance of primary post- tonsillectomy hemorrhage in a teaching program. Arch Otolaryngol Head Neck Surg . 1999;125(3):330- 333.

were more objective than level I (self- reported) bleeding and are associated with greater risk to patients. Although we counseled all of our parents to re- port any bleeding event, many pa- tients with level I bleeding events were nondescript and self-limited. In the ma- jority of these cases, parents did not re- port bleeding events until the fol- low-up appointment, and then only when prompted by the questionnaire. This was explained by the minor or questionable nature of these bleeding events. Some examples included a “warm sensation in the mouth” or a “bloodstain on a pillow case.” The level II and III postoperative bleeding events are a more reliable indicator for com- plications because they are docu- mented by treating physicians. These events are also associated with substan- tial morbidity and cost that occurs with prolonged hospitalization and the need for reoperations. An inappropriately selected, nonin- feriority margin can result in an im- properly powered study. We used level II and III bleeding events to establish our study size because these events are more objective and clinically impor- tant than level I bleeding events. We used our institutions’ outcomes data for level II and II bleeding events coupled with published literature reports to de- termine the noninferioritymargin of 5% for our study. We were limited in this approach because most published stud- ies did not report bleeding severity. Other potential limitations include the use of multiple surgeons and institu- tions. Standardization of procedures should have minimized the effect of this potential limitation. We did not stratify dosing of dexamethasone.We only used a single, routinely used dose that was commonly cited in the literature. Graded dexamethasone doses would have required a much larger sample size, diminishing the feasibility of com- pleting this study. In conclusion, in this prospective, randomized study of 314 children un- dergoing tonsillectomy, perioperative dexamethasone administration was not associated with more level II or III

bleeding events than placebo as shown by noninferiority. Increased subjec- tive (level I) bleeding events caused by dexamethasone could not be ex- cluded because the noninferiority threshold of 5% was crossed. Author Contributions: Drs Gallagher and Hartnick had full access to all of the data in the study and take re- sponsibility for the integrity of the data and the ac- curacy of the data analysis. Study concept and design: Gallagher, Ference, Keamy, Hartnick. Acquisition of data: Gallagher, Hill, Ojha, Keamy, Williams, Hansen, Collins, Setlur, Capra, Brigger, Hartnick. Analysis and interpretation of data: Gallagher, Hill, Ojha, Maurer, Brigger. Drafting of the manuscript: Gallagher, Ference, Collins, Setlur, Hartnick. Critical revision of the manuscript for important in- tellectual content: Gallagher, Hill, Ojha, Ference, Keamy, Williams, Hansen, Maurer, Setlur, Capra, Brigger, Hartnick. Statistical analysis: Ference, Maurer, Brigger, Hartnick. Administrative, technical, or material support: Gallagher, Hill, Ference, Collins, Setlur, Capra. Study supervision: Gallagher, Keamy, Brigger, Hartnick. Conflict of Interest Disclosures: All authors have com- pleted and submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Dr Hartnick re- ported receiving consultancy fees from Gyrus ACMI, receiving a grant from the National Institutes of Health to study voice disorders and voice therapy in children with vocal dysphonia, and receiving book royalties from Springer. No other authors reported any disclosures. Disclaimer: The views expressed in this article are those of the authors and do not necessarily reflect the offi- cial policy or position of the US Department of the Navy, US Department of Defense, or the US government. Online-Only Material: eMethods is available at http: //www.jama.com. Additional Contributions: Michael Cunningham, MD (Boston Children’s Hospital, Boston, Massachusetts), and Donna Neuberg, PhD (Harvard School of Public Health, Boston, Massachusetts), provided comments on the analysis of the manuscript; James Ware, PhD (Harvard School of Public Health, Boston, Massachu- setts), provided comments on the design of the manu- script; and Christine Finn, PhD (Massachusetts Eye and Ear Infirmary, Boston, Massachusetts), Cheryl McNeal (Naval Medical Center, San Diego, California), Van- essa DeGuzman (Massachusetts Eye and Ear Infir- mary, Boston, Massachusetts), and David Baxter (Har- vard Vanguard Associates, Boston, Massachusetts) helped with the acquisition of data. Drs Cunning- ham, Ware, and Neuberg received no compensation and Dr Finn, Ms McNeal, Ms DeGuzman, andMr Bax- ter were all compensated for their contributions. REFERENCES 1. Centers for Disease Control and Prevention. Ad- vance Data 283: Ambulatory Surgery in the United States, 1994. http://www.cdc.gov/nchs/data/ad /ad283.pdf. Accessed June 18, 2012. 2. Centers for Disease Control and Prevention. Am- bulatory Surgery in the United States, 2006. http: //www.cdc.gov/nchs/data/nhsr/nhsr011.pdf. Ac- cessed June 18, 2012. 3. Randall DA, Hoffer ME. Complications of tonsil- lectomy and adenoidectomy. Otolaryngol Head Neck Surg . 1998;118(1):61-68. 4. Kim MS, Cote´ CJ, Cristoloveanu C, et al. There is no dose-escalation response to dexamethasone (0.0625-1.0 mg/kg) in pediatric tonsillectomy or ad-

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