Eberhart L H J, Büning E Kleine, Folz B, Maybauer D M, Kästner M, Kalder M, Koch T, Kranke P, Wulf H
Department of Anaesthesiology and Intensive Care, University Hospital Giessen-Marburg, Marburg, Germany.
Eur J Clin Invest. 2006 Aug;36(8):580-7. doi: 10.1111/j.1365-2362.2006.01671.x.
The corticosteroid dexamethasone and the serotonine3 -antagonist tropisetron are both effective drugs for the prophylaxis of post-operative nausea and vomiting (PONV) when given intravenously. The aim of this trial was to evaluate the oral use of both drugs as part of a routine oral premedication and to compare their single and combined effectiveness.
In this randomized, placebo-controlled, double-blind study, 320 inpatients with a moderate-high risk of PONV (> or = 40% according to two validated risk scores) received an oral premedication 1-2 h pre-operatively with placebo, a fixed dose of tropisetron 5 mg, dexamethasone 8 mg, or a combination of both drugs. A standardized general anaesthesia was performed, including benzodiazepine premedication, propofol, rocuronium, desflurane in air/O2, fentanyl or sufentanil followed by a continuous infusion of remifentanil. Post-operative analgesia and anti-emetic rescue medication were standardized. The main outcome measures were the severity of PONV within the first 24 h (rated by a standardized scoring algorithm). The incidence of PONV was used as the secondary outcome.
Data from 310 patients were analyzed. The mean severity score in the placebo-, tropisetron-, dexamethasone- and the combined-groups was 1.37, 0.8, 0.8 and 0.38, respectively. The incidence of PONV of any severity was 59.2%, 37.5%, 40% and 22.8%, respectively. The reduction of the incidence and the severity of PONV were statistically significant with all three interventions. Results from additional analyses suggested that both drugs were equally effective and that there was a simple additive effect of tropisetron and dexamethasone compared with placebo.
Oral tropisetron and dexamethasone were both equally effective in reducing the severity and incidence of post-operative nausea and vomiting. The latter could be reduced by approximately 35% in a population of moderate-high risk for PONV. Both drugs had an additive effect. However, even in the combination group there still remained an unacceptably high incidence of PONV of more than 20%. This highlighted the need for a multimodal anti-emetic approach in high-risk patients and the importance of treatment of PONV.
皮质类固醇地塞米松和5-羟色胺3拮抗剂托烷司琼静脉给药时均是预防术后恶心呕吐(PONV)的有效药物。本试验旨在评估这两种药物作为常规口服术前用药的效果,并比较它们单独使用及联合使用的有效性。
在这项随机、安慰剂对照、双盲研究中,320例中度至高度PONV风险(根据两项有效风险评分≥40%)的住院患者在术前1 - 2小时接受口服术前用药,用药分别为安慰剂、固定剂量5毫克托烷司琼、8毫克地塞米松或两种药物的组合。实施标准化全身麻醉,包括苯二氮䓬类术前用药、丙泊酚、罗库溴铵、空气/氧气中的地氟醚、芬太尼或舒芬太尼,随后持续输注瑞芬太尼。术后镇痛和止吐抢救用药标准化。主要观察指标为术后24小时内PONV的严重程度(通过标准化评分算法评定)。PONV的发生率用作次要观察指标。
分析了310例患者的数据。安慰剂组、托烷司琼组、地塞米松组和联合用药组的平均严重程度评分分别为1.37、0.8、0.8和0.38。任何严重程度的PONV发生率分别为59.2%、37.5%、40%和22.8%。所有三种干预措施在降低PONV发生率和严重程度方面均具有统计学意义。额外分析结果表明,两种药物效果相当,与安慰剂相比,托烷司琼和地塞米松具有简单的相加效应。
口服托烷司琼和地塞米松在降低术后恶心呕吐的严重程度和发生率方面同样有效。在中度至高度PONV风险人群中,后者可降低约35%。两种药物具有相加效应。然而,即使在联合用药组中,PONV发生率仍高达20%以上,令人难以接受。这凸显了高危患者采用多模式止吐方法的必要性以及治疗PONV的重要性。