Sinha Renu, Shende Dilip, Maitra Souvik, Kumar Neeraj, Ray Bikash Ranjan, Mohan Virender Kumar
Room Number 376, Dr. R. P. Centre for Ophthalmic Sciences, AIIMS, New Delhi, India.
Room Number 374, Dr. R. P. Centre for Ophthalmic Sciences, AIIMS, New Delhi, India.
Anesthesiol Res Pract. 2016;2016:4281719. doi: 10.1155/2016/4281719. Epub 2016 Jan 26.
Aim. Efficacy of granisetron and combination of granisetron and dexamethasone was evaluated for prevention of postoperative nausea and vomiting (PONV) in children undergoing elective strabismus surgery. Methods. A total of 136 children (1-15 years) were included. Children received either granisetron (40 mcg/kg) [group G] or combination of granisetron (40 mcg/kg) and dexamethasone (150 mcg/kg) [group GD]. Intraoperative fentanyl requirement and incidence and severity of oculocardiac reflex were assessed. PONV severity was assessed for first 24 hours and if score was >2, it was treated with metoclopramide. Postoperative analgesia was administered with intravenous fentanyl and ibuprofen. Results. The demographic profile, muscles operated, and fentanyl requirement were comparable. Complete response to PONV in first 24 hours was observed in 75% (51/68) of children in group G and 76.9% (50/65) of children in group GD, which was comparable statistically (p = 0.96, Fisher exact test; OR 1.11, 95% CI 0.50, 2.46). Incidence of PONV between 0 and 24 hours was comparable. One child in group G required rescue antiemetic in first 24 hours and none of the children had severe PONV in group GD. There was no significant difference in incidence or severity of oculocardiac reflex. Conclusion. Dexamethasone did not increase efficacy of granisetron for prevention of PONV in elective pediatric strabismus surgery. Registration number of clinical trial was CTRI/2009/091/001000.
目的。评估格拉司琼以及格拉司琼与地塞米松联合用药对择期斜视手术儿童术后恶心呕吐(PONV)的预防效果。方法。共纳入136名1至15岁儿童。儿童分别接受格拉司琼(40微克/千克)[G组]或格拉司琼(40微克/千克)与地塞米松(150微克/千克)联合用药[GD组]。评估术中芬太尼需求量以及眼心反射的发生率和严重程度。对术后首24小时的PONV严重程度进行评估,若评分>2,则用甲氧氯普胺治疗。术后镇痛采用静脉注射芬太尼和布洛芬。结果。人口统计学特征、手术肌肉以及芬太尼需求量具有可比性。G组75%(51/68)的儿童和GD组76.9%(50/65)的儿童在术后首24小时对PONV完全缓解,统计学上具有可比性(p = 0.96,Fisher精确检验;OR 1.11,95% CI 0.50,2.46)。0至24小时之间PONV的发生率具有可比性。G组有1名儿童在术后首24小时需要急救止吐药,GD组无儿童发生严重PONV。眼心反射的发生率和严重程度无显著差异。结论。在择期小儿斜视手术中,地塞米松未增加格拉司琼预防PONV的疗效。临床试验注册号为CTRI/2009/091/001000。