Ploner F, Kainzwaldner A
Abteilung für Anästhesie und allgemeine Intensivmedizin, Landeskrankenhaus Brixen.
Anaesthesist. 1997 Jul;46(7):583-7. doi: 10.1007/s001010050440.
To investigate the incidence of postoperative nausea and vomiting (PONV) depending on the administration time of ondansetron.
In this prospective, double-blind, parallel-group study we compared the prevention of PONV with ondansetron at two administration times versus placebo in 120 patients undergoing balanced general anaesthesia. The patients were stratified according to the type of surgery and randomly allocated to three treatment groups: 40 patients (Group A) received ondansetron 4 mg i.v. 10 min before the induction of anaesthesia and placebo 10 min before the end of surgery; 40 (Group B) received placebo 10 min before the induction of anaesthesia and ondansetron 4 mg i.v. 10 min before the end of surgery; and 40 (Group C) received placebo at both of the administrations. Data were analysed by Student's t-test and chi-square test; significance was taken at P < 0.05.
The analyses of the results showed a significantly lower incidence of PONV in treated patients (Groups A and B) than in the control group (Group C): postoperative nausea occurred in 12.5%, 27.5%, and 65% of patients in Groups A, B, and C, respectively, and was associated with vomiting in Group A in 2.5% Group B in 5%, and Group C in 55% of patients. Although the patients in Group A showed a lower incidence of PONV in comparison to those in Group B, the difference was not statistically significant.
The incidence of PONV was significantly lower in the groups with administration of 4 mg ondansetron. Ondansetron is therefore safe and affective in preventing PONV in surgical patients. The administration time does not influence the occurrence of PONV.
探讨昂丹司琼给药时间对术后恶心呕吐(PONV)发生率的影响。
在这项前瞻性、双盲、平行组研究中,我们比较了120例接受平衡全身麻醉患者中,两个给药时间点使用昂丹司琼预防PONV与使用安慰剂的效果。患者根据手术类型分层,随机分为三个治疗组:40例患者(A组)在麻醉诱导前10分钟静脉注射4毫克昂丹司琼,在手术结束前10分钟静脉注射安慰剂;40例患者(B组)在麻醉诱导前10分钟静脉注射安慰剂,在手术结束前10分钟静脉注射4毫克昂丹司琼;40例患者(C组)在两个给药时间点均静脉注射安慰剂。数据采用学生t检验和卡方检验进行分析;P<0.05为有统计学意义。
结果分析显示,治疗组(A组和B组)的PONV发生率显著低于对照组(C组):A组、B组和C组患者术后恶心的发生率分别为12.5%、27.5%和65%,A组、B组和C组患者中伴有呕吐的比例分别为2.5%、5%和55%。虽然A组患者的PONV发生率低于B组,但差异无统计学意义。
给予4毫克昂丹司琼的组中PONV发生率显著较低。因此,昂丹司琼在预防手术患者PONV方面安全有效。给药时间不影响PONV的发生。