首页> 美国卫生研究院文献>Anesthesiology Research and Practice >Granisetron versus Granisetron-Dexamethasone for Prevention of Postoperative Nausea and Vomiting in Pediatric Strabismus Surgery: A Randomized Double-Blind Trial
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Granisetron versus Granisetron-Dexamethasone for Prevention of Postoperative Nausea and Vomiting in Pediatric Strabismus Surgery: A Randomized Double-Blind Trial

机译:Granisetron与Granisetron-地塞米松预防小儿斜视手术后恶心和呕吐的预防:一项随机双盲试验

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摘要

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 .
机译:目标。评估了格拉司琼以及格拉司琼与地塞米松联合使用对预防性斜视手术患儿术后恶心和呕吐(PONV)的疗效。方法。总共包括136名儿童(1至15岁)。儿童接受Granisetron(40 mcg / kg)[G组]或Granisetron(40 mcg / kg)和地塞米松(150 mcg / kg)[GD组]的组合。评估术中芬太尼的需求量以及眼心反射的发生率和严重程度。在开始的24小时内评估PONV的严重程度,如果评分> 2,则用甲氧氯普胺治疗。术后采用静脉芬太尼和布洛芬镇痛。结果。人口统计学特征,操作的肌肉和芬太尼需求量可比。 G组75%(51/68)的儿童和GD组76.9%(50/65)的儿童在开始的24小时内对PONV完全反应,这在统计学上具有可比性(p = 0.96,Fisher精确检验;或1.11,95%CI 0.50,2.46)。 PONV在0到24小时之间的发生率是可比的。 G组中的一名儿童在开始的24小时内需要服用止吐药,而GD组中没有一名儿童患有严重的PONV。眼动反射的发生率或严重程度无明显差异。结论。地塞米松在选择性小儿斜视手术中并未增加Granisetron预防PONV的疗效。临床试验注册号为。

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