Fujii Y, Saitoh Y, Kobayashi N
Department of Anesthesiology, Toride Kyodo General Hospital, Tosride City, Ibaraki, Japan.
Laryngoscope. 2001 Feb;111(2):255-8. doi: 10.1097/00005537-200102000-00013.
OBJECTIVE/HYPOTHESIS: Granisetron, a selective 5-hydroxytryptamine type 3 receptor antagonist, is effective for the prevention of vomiting after tonsillectomy in children. Ramosetron (Nasea; Yamanouchi; Tokyo, Japan), another new antagonist of 5-hydroxytryptamione type 3 receptor, has more potent and longer-acting properties than granisetron (Kytril; Smith Kline Beecham, London, UK) against cisplatin-induced emesis. This study was undertaken to compare the efficacy and safety of granisetron and ramosetron for the prevention of vomiting after pediatric tonsillectomy.
Prospective, randomized, double-blinded study.
Ninety pediatric patients, aged 4 to 10 years, received intravenously granisetron 40 microg/kg or ramosetron 6 microg/kg (n = 45 each) at the end of surgery. The same standard general anesthetic technique and postoperative analgesia were used throughout. Emetic episodes and safety assessment were performed during the first 24-hour period and the next 24-hour period after anesthesia.
The rates of patients being emesis-free during the period from 0 to 24 hours after anesthesia were 89% with granisetron and 93% with ramosetron, respectively (P = .357); the corresponding rates during the period from 24 to 48 hours after anesthesia were 71% and 93%, respectively (P = .006). No clinically serious adverse events attributable to the study drugs were observed in any of the groups.
Ramosetron is a better antiemetic than granisetron for the long-term prevention of postoperative vomiting in children undergoing general anesthesia for tonsillectomy.
目的/假设:格拉司琼是一种选择性5-羟色胺3型受体拮抗剂,对预防儿童扁桃体切除术后呕吐有效。雷莫司琼(Nasea;日本山之内制药公司;东京)是另一种新型5-羟色胺3型受体拮抗剂,在对抗顺铂引起的呕吐方面比格拉司琼(Kytril;英国史克必成公司;伦敦)具有更强效和长效的特性。本研究旨在比较格拉司琼和雷莫司琼预防小儿扁桃体切除术后呕吐的疗效和安全性。
前瞻性、随机、双盲研究。
90例4至10岁的儿科患者在手术结束时静脉注射40微克/千克格拉司琼或6微克/千克雷莫司琼(每组n = 45)。整个过程采用相同的标准全身麻醉技术和术后镇痛方法。在麻醉后的前24小时和接下来的24小时内进行呕吐发作情况和安全性评估。
麻醉后0至24小时期间无呕吐患者的比例,格拉司琼组为89%,雷莫司琼组为93%(P = 0.357);麻醉后24至48小时期间相应比例分别为71%和93%(P = 0.006)。在任何一组中均未观察到归因于研究药物的临床严重不良事件。
对于接受扁桃体切除全身麻醉的儿童,雷莫司琼在长期预防术后呕吐方面比格拉司琼更有效。