Department of Anesthesiology and Pain Medicine, Seoul National University Bundang Hospital, 166 Kumi-ro, Bundang-gu, Seongnam-si, Kyonggi-do, 463-707, South Korea.
Surg Endosc. 2010 Apr;24(4):812-7. doi: 10.1007/s00464-009-0670-5. Epub 2009 Aug 26.
Patients undergoing general anesthesia for laparoscopic cholecystectomy are at high risk for postoperative nausea and vomiting (PONV). This study compared ramosetron and ondansetron in terms of efficacy for PONV prevention after laparoscopic cholecystectomy.
For this study, 120 patients scheduled to undergo laparoscopic cholecystectomy were randomized (in double-blind fashion) to receive 4 mg of ondansetron (group O4, n = 40), 8 mg of ondansetron (group O8, n = 40), or 0.3 mg of ramosetron (group R, n = 40) intravenously after surgery. Postoperative nausea, retching, vomiting, pain, and side effects were assessed at 2 h, 24 h, and 48 h after surgery.
No statistical differences were observed among the three groups with regard to patient characteristics and information on surgery and anesthesia. The ratio of complete response (no PONV for 2 h) was higher for groups O8 and R than for group O4 as follows: 80% (n = 32) for groups O8 and R versus 58% (n = 23) for group O4 during the first postoperative 2 h (p = 0.04), 90% (n = 36) for groups O8 and R versus 76% (n = 30) for group O4 over 24 h (2-24 h) (p = 0.09), and 98% (n = 38) for groups O4 and O8 versus 100% (n = 40) for group R over the next 24 h (24-48 h) after surgery (p = 0.36). During the first 2 h after surgery, rescue antiemetics were used for significantly fewer patients in groups O8 and R (20%) than in group O4 (42.5%) (p = 0.04). Postoperative pain and the use of rescue analgesics were comparable among the groups. There was no clinically serious adverse event due to the study drugs.
Ramosetron 0.3 mg and ondansetron 8 mg are more effective than ondansetron 4 mg for the prevention of PONV (2 h). Ramosetron 0.3 mg is as effective as ondansetron 8 mg for the prophylaxis of PONV after laparoscopic cholecystectomy.
接受腹腔镜胆囊切除术全身麻醉的患者发生术后恶心呕吐(PONV)的风险较高。本研究比较了雷莫司琼和昂丹司琼在预防腹腔镜胆囊切除术后 PONV 方面的疗效。
本研究中,120 例拟行腹腔镜胆囊切除术的患者随机(双盲)接受静脉注射 4 mg 昂丹司琼(O4 组,n=40)、8 mg 昂丹司琼(O8 组,n=40)或 0.3 mg 雷莫司琼(R 组,n=40)。术后 2 h、24 h 和 48 h 评估术后恶心、呕吐、疼痛和不良反应。
三组患者的一般特征、手术和麻醉信息均无统计学差异。O8 组和 R 组完全缓解(术后 2 h 无 PONV)的比例明显高于 O4 组,如下所示:O8 组和 R 组的完全缓解比例分别为 80%(n=32)和 90%(n=36),O4 组为 58%(n=23)(p=0.04);O8 组和 R 组在术后 24 h(2-24 h)时的完全缓解比例分别为 90%(n=36)和 98%(n=38),O4 组为 76%(n=30)(p=0.09);O8 组和 R 组在术后 24-48 h(24-48 h)时的完全缓解比例分别为 98%(n=38)和 100%(n=40),O4 组为 76%(n=30)(p=0.36)。在术后 2 h 内,O8 组和 R 组使用止吐药的患者明显少于 O4 组(20% vs 42.5%)(p=0.04)。三组患者术后疼痛和使用解救性镇痛药的情况相似。研究药物未发生临床严重不良事件。
雷莫司琼 0.3 mg 和昂丹司琼 8 mg 比昂丹司琼 4 mg 更有效预防 PONV(2 h)。雷莫司琼 0.3 mg 与昂丹司琼 8 mg 预防腹腔镜胆囊切除术后 PONV 的效果相当。