Agarkar Sandip, Chatterjee Aparna S
Department of Anesthesia, Critical Care and Pain, Tata Memorial Hospital, Parel, Mumbai, Maharashtra, India.
Indian J Anaesth. 2015 Apr;59(4):222-7. doi: 10.4103/0019-5049.154999.
Post-operative nausea and vomiting (PONV) has an 80% incidence in high-risk patients. This is despite the availability of several antiemetic drugs. Selective 5-hydroxytryptamine type 3 (5-HT3) receptor antagonists are considered first-line for prophylaxis, ondansetron being the most commonly used agent. Ramosetron, another selective 5-HT3 receptor antagonist, is more potent and longer acting than ondansetron. This study was conducted to evaluate the antiemetic efficacy of ramosetron in comparison with ondansetron in patients at a high risk of PONV.
This was a prospective randomised double-blind study carried out over a 6-month period in which 206 patients with at least two risk factors for PONV were randomised to receive ramosetron 0.3 mg or ondansetron 8 mg, 30 min before the end of surgery. The incidence of PONV, severity of nausea and need for rescue antiemetic were recorded over the next 24 h. Primary outcome was the incidence of PONV. Secondary outcomes included severity of nausea and need for rescue. The data were analysed using the Predictive Analytics Software (PASW, version 18: Chicago, IL, USA).
The incidence of PONV was found to be 35% in the ramosetron group as opposed to 43.7% in the ondansetron group (P = 0.199). Need for rescue antiemetic was 23.3% in the ramosetron group and 32% in the ondansetron group (P = 0.156) in the 24 h following surgery.
Ramosetron 0.3 mg and ondansetron 8 mg were equally effective in reducing the incidence of PONV in high risk patients.
术后恶心呕吐(PONV)在高危患者中的发生率为80%。尽管有多种止吐药物可供使用。选择性5-羟色胺3型(5-HT3)受体拮抗剂被认为是预防的一线用药,昂丹司琼是最常用的药物。雷莫司琼,另一种选择性5-HT3受体拮抗剂,比昂丹司琼更有效且作用时间更长。本研究旨在评估雷莫司琼与昂丹司琼相比对PONV高危患者的止吐疗效。
这是一项前瞻性随机双盲研究,为期6个月,206例至少有两个PONV危险因素的患者在手术结束前30分钟被随机分为接受0.3毫克雷莫司琼或8毫克昂丹司琼治疗。在接下来的24小时内记录PONV的发生率、恶心的严重程度以及使用抢救性止吐药的需求。主要结局是PONV的发生率。次要结局包括恶心的严重程度和使用抢救性药物的需求。使用预测分析软件(PASW,版本18:美国伊利诺伊州芝加哥)对数据进行分析。
雷莫司琼组PONV的发生率为35%,而昂丹司琼组为43.7%(P = 0.199)。术后24小时内,雷莫司琼组使用抢救性止吐药的需求为23.3%,昂丹司琼组为32%(P = 0.156)。
0.3毫克雷莫司琼和8毫克昂丹司琼在降低高危患者PONV发生率方面同样有效。