Karaman Murat, Ilhan Adem Emre, Dereci Gökçe, Tek Arman
The Department of Otorhinolaryngology at Umraniye State Hospital for Research and Training, Istanbul, Turkey.
Int J Pediatr Otorhinolaryngol. 2009 Nov;73(11):1513-5. doi: 10.1016/j.ijporl.2009.06.001. Epub 2009 Jul 10.
Our objective is to determine the optimum dosage of intraoperative single dose dexamethasone and its effect upon postoperative morbidity in pediatric tonsillectomy and adenotonsillectomy patients.
Totally 150 pediatric patients whom underwent adenotonsillectomy or tonsillectomy surgery are offered to participate in this study at otorhinolaryngology clinic between 2002 and 2003. 150 patients are divided into three randomized groups, each composed of fifty patients. Anesthesia protocol is standardized in each group and 0.2 mg/kg intraoperative dexamethasone is given to first group, 0.7 mg/kg (maximum dose 25 mg) intraoperative dexamethasone is given to second group and third group is accepted as control group without giving any intravenous dexamethasone. Each group is compared for postoperative nausea, vomiting and tolerability to take oral foods within first 24h with the same questionnaire.
There is significantly higher ratio of postoperative nausea and vomiting within first 24h in group III (80%) when compared with group I (8%) (p: 0.001; p<0.01) and group II (4%) (p: 0.001; p<0.01). Also there is significantly higher ratio of patient's tolerability to take oral semisolid/solid foods within postoperative first 24h in group II (94%) when compared with group I (58%) (p: 0.001; p<0.01) and group III (12%) (p: 0.001; p<0.01). We didn't encounter any side effect of dexamethasone in group I and II.
We thought that 0.7 mg/kg dosage of IV dexamethasone is much a preferable choice depending of its effectiveness on decreasing postoperative morbidity rather than 0.2 mg/kg dosage and beside to this advantage we didn't encounter any side effects.
我们的目的是确定小儿扁桃体切除术和腺样体扁桃体切除术患者术中单次使用地塞米松的最佳剂量及其对术后发病率的影响。
2002年至2003年期间,共有150例接受腺样体扁桃体切除术或扁桃体切除术的小儿患者在耳鼻喉科门诊被邀请参与本研究。150例患者被随机分为三组,每组50例。每组的麻醉方案标准化,第一组术中给予0.2mg/kg地塞米松,第二组术中给予0.7mg/kg(最大剂量25mg)地塞米松,第三组作为对照组,不给予任何静脉用地塞米松。使用相同的问卷对每组术后24小时内的恶心、呕吐情况以及口服食物的耐受性进行比较。
与第一组(8%)(p:0.001;p<0.01)和第二组(4%)(p:0.001;p<0.01)相比,第三组术后24小时内恶心和呕吐的发生率显著更高(80%)。此外,与第一组(58%)(p:0.001;p<0.01)和第三组(12%)(p:0.001;p<0.01)相比,第二组术后24小时内患者口服半固体/固体食物的耐受性显著更高(94%)。第一组和第二组未出现地塞米松的任何副作用。
我们认为,静脉注射地塞米松0.7mg/kg的剂量比0.2mg/kg的剂量更可取,因为它在降低术后发病率方面更有效,而且除此之外我们没有遇到任何副作用。