A comparative study between 1 and 3 mg of granisetron in the prevention of postoperative nausea and vomiting in strabismus ophthalmic surgeries during general anesthesia

T. Khair, M. Ahmed, A. Mohamed, I. Sayed, Tamer Saafan
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Abstract

Aims To compare the safety and efficacy of 1 and 3 mg of granisetron in the prevention of postoperative nausea and vomiting (PONV) in strabismus surgeries under general anesthesia. Settings and design This single-blinded, randomized, controlled trial was conducted at the ophthalmology operating theater of Kasr Al-Ainy Hospitals. Patients and methods We recruited 210 patients and allocated them randomly to receive either granisetron 1 mg (n=105) or 3 mg (n=105). The two groups were compared regarding demographic data, hemodynamic parameters, and percentage of patients with no complaints of PONV during the first 24 h. Results There was no statistically significant difference upon comparison of the two groups regarding PONV (P>0.05). The two doses (1 and 3 mg) provided total control of nausea and vomiting in 46.7 and 43.8% of patients during the first 24 h postoperatively, respectively. Moreover, we found no significant difference between the two groups regarding mean values of the heart rate or mean arterial pressure both preoperatively and intraoperatively (P>0.05). However, during the postoperative 24 h, both groups had significant differences regarding mean values of heart rate and mean arterial pressure at 2–4 h, 8–12 h, and 12–24 h postoperatively. Conclusions The comparison between two doses of granisetron (1 and 3 mg) showed no statistical difference regarding the total control of nausea and vomiting for 24 h postoperatively but showed a statistical difference regarding some postoperative vital sign readings.
1和3mg格拉司琼预防斜视术后全身麻醉下恶心呕吐的比较研究
目的比较1、3mg格拉司琼预防斜视手术全麻下术后恶心呕吐(PONV)的安全性和有效性。本单盲、随机、对照试验在Kasr Al-Ainy医院眼科手术室进行。患者和方法我们招募了210例患者,并将他们随机分配到格拉司琼1mg (n=105)或3mg (n=105)组。比较两组患者的人口学数据、血流动力学参数和前24小时无PONV主诉的患者百分比。结果两组PONV比较,差异无统计学意义(P>0.05)。两种剂量(1和3mg)在术后24小时内分别为46.7%和43.8%的患者提供恶心和呕吐的完全控制。两组患者术前、术中心率平均值、平均动脉压均无统计学差异(P>0.05)。然而,在术后24小时内,两组在术后2-4小时、8-12小时和12-24小时的心率和平均动脉压平均值有显著差异。结论格拉司琼1和3mg两种剂量对术后24 h恶心呕吐的总控制无统计学差异,但在术后一些生命体征指标上有统计学差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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