Department of Anesthesiology and Pain Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Yonsei Med J. 2010 Jan;51(1):88-92. doi: 10.3349/ymj.2010.51.1.88. Epub 2009 Dec 29.
We compared the prophylactic effects of intravenously administered azasetron (10 mg) and ondansetron (8 mg) on postoperative nausea and vomiting (PONV) in patients undergoing gynecological laparoscopic surgery under general anesthesia.
We studied 98 ASA physical status I or II 20-65 years old, female patients, in this prospective, randomized, double blind study. Patients were randomly divided into two groups and received ondansetron 8 mg (group O) or azasetron 10 mg (group A) 5 min before the end of surgery. The incidence of PONV, Visual Analogue Scale (VAS) for pain, need for rescue antiemetic and analgesics, and adverse effects were checked at 1, 6, 12, 24, and 48 h postoperatively.
The overall incidence of PONV was 65% in group O and 49% in group A. The incidence of PONV was significantly higher in group O than in group A at 12-24 h postoperatively (nausea; 24% vs. 45%, p = 0.035, vomiting; 2% vs. 18%, p = 0.008), but there were no significant differences at 0-1, 1-6, 6-12 or 24-48 h.
In conclusion, azasetron (10 mg) produced same incidence of PONV as ondansetron (8 mg) in patients undergoing general anesthesia for gynecological laparoscopic surgery. Azasetron was more effective, in the intermediate post-operative period, between 12 and 24 h.
我们比较了静脉给予阿扎司琼(10mg)和昂丹司琼(8mg)对全麻下妇科腹腔镜手术患者术后恶心和呕吐(PONV)的预防作用。
我们前瞻性、随机、双盲研究了 98 例 ASA 身体状况 I 或 II 级、20-65 岁的女性患者。患者随机分为两组,在手术结束前 5 分钟分别接受昂丹司琼 8mg(O 组)或阿扎司琼 10mg(A 组)。在术后 1、6、12、24 和 48 小时检查 PONV 的发生率、疼痛视觉模拟量表(VAS)评分、需要解救性止吐药和镇痛药以及不良反应。
O 组 PONV 的总发生率为 65%,A 组为 49%。O 组在术后 12-24 小时 PONV 的发生率明显高于 A 组(恶心:24% vs. 45%,p = 0.035,呕吐:2% vs. 18%,p = 0.008),但在 0-1、1-6、6-12 或 24-48 小时时无显著差异。
总之,阿扎司琼(10mg)在全麻下妇科腹腔镜手术中引起的 PONV 发生率与昂丹司琼(8mg)相同。在术后 12-24 小时,阿扎司琼的疗效更为显著。