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在门诊环境中,昂丹司琼给药时间对其作为预防性止吐药的疗效、成本效益和成本效益的影响。

The effect of timing of ondansetron administration on its efficacy, cost-effectiveness, and cost-benefit as a prophylactic antiemetic in the ambulatory setting.

作者信息

Tang J, Wang B, White P F, Watcha M F, Qi J, Wender R H

机构信息

Department of Anesthesiology and Pain Management, University of Texas Southwestern Medical Center at Dallas, 75235-9068, USA.

出版信息

Anesth Analg. 1998 Feb;86(2):274-82. doi: 10.1097/00000539-199802000-00010.

Abstract

UNLABELLED

Although ondansetron (4 mg I.V.) is effective in the prevention and treatment of postoperative nausea and vomiting (PONV) after ambulatory surgery, the optimal timing of its administration, the cost-effectiveness, the cost-benefits, and the effect on the patient's quality of life after discharge have not been established. In this placebo-controlled, double-blind study, 164 healthy women undergoing outpatient gynecological laparoscopic procedures with a standardized anesthetic were randomized to receive placebo (Group A), ondansetron 2 mg at the start of and 2 mg after surgery (Group B), ondansetron 4 mg before induction (Group C), or ondansetron 4 mg after surgery (Group D). The effects of these regimens on the incidence, severity, and costs associated with PONV and discharge characteristics were determined, along with the patient's willingness to pay for antiemetics. Compared with ondansetron given before induction of anesthesia, the administration of ondansetron after surgery was associated with lower nausea scores, earlier intake of normal food, decreased incidence of frequent emesis (more than two episodes), and increased times until 25% of patients failed prophylactic antiemetic therapy (i.e., had an emetic episode or received rescue antiemetics for severe nausea) during the first 24 h postoperatively. This prophylactic regimen was also associated with the highest patient satisfaction and lowest cost-effectiveness ratios. Compared with the placebo group, ondansetron administered after surgery significantly reduced the incidence of PONV in the postanesthesia care unit and during the 24-h follow-up period and facilitated the recovery process by reducing the time to oral intake, ambulation, discharge readiness, resuming regular fluid intake and a normal diet. When ondansetron was given as a "split dose," its prophylactic antiemetic efficacy was not significantly different from that of the placebo group. In conclusion, the prophylactic administration of ondansetron after surgery, rather than before induction, may be associated with increased patient benefits.

IMPLICATIONS

Ondansetron 4 mg I.V. administered immediately before the end of surgery was the most efficacious in preventing postoperative nausea and vomiting, facilitating both early and late recovery, and improving patient satisfaction after outpatient laparoscopy.

摘要

未标记

尽管昂丹司琼(4毫克静脉注射)在预防和治疗门诊手术后的恶心和呕吐(PONV)方面有效,但其给药的最佳时机、成本效益、成本效益以及对出院后患者生活质量的影响尚未确定。在这项安慰剂对照、双盲研究中,164名接受标准化麻醉的门诊妇科腹腔镜手术的健康女性被随机分为接受安慰剂(A组)、手术开始时给予2毫克昂丹司琼且术后给予2毫克(B组)、诱导前给予4毫克昂丹司琼(C组)或术后给予4毫克昂丹司琼(D组)。确定了这些方案对PONV的发生率、严重程度、相关成本和出院特征的影响,以及患者购买止吐药的意愿。与麻醉诱导前给予昂丹司琼相比,术后给予昂丹司琼与较低的恶心评分、更早摄入正常食物、频繁呕吐(超过两次发作)的发生率降低以及术后24小时内直到25%的患者预防性止吐治疗失败(即有呕吐发作或因严重恶心接受抢救性止吐药)的时间增加有关。这种预防方案还与最高的患者满意度和最低的成本效益比相关。与安慰剂组相比,术后给予昂丹司琼显著降低了麻醉后护理单元和24小时随访期间PONV的发生率,并通过减少口服摄入时间、下床活动时间、出院准备时间、恢复正常液体摄入和正常饮食促进了恢复过程。当昂丹司琼作为“分剂量”给药时,其预防性止吐疗效与安慰剂组无显著差异。总之,术后预防性给予昂丹司琼而非诱导前给药可能会增加患者受益。

启示

手术结束前立即静脉注射4毫克昂丹司琼在预防门诊腹腔镜术后恶心和呕吐、促进早期和晚期恢复以及提高患者满意度方面最有效。

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