Department of Anesthesiology, Duke University Medical Center, CB 3094, Durham, NC 27710, USA.
Anesth Analg. 2011 Apr;112(4):804-12. doi: 10.1213/ANE.0b013e31820886c3. Epub 2011 Mar 8.
Postoperative nausea and vomiting (PONV) are common complications after surgery. Neurokinin-1 (NK(1)) receptor antagonists have been shown to be safe and effective for the prevention and treatment of PONV in humans. Rolapitant is a potent, selective NK1 receptor antagonist that is rapidly absorbed, has a remarkably long half-life (up to180 hours), and appears to have a low potential for drug-drug interactions. We evaluated the dose response for rolapitant for the prevention of PONV in subjects at high risk for this condition, and rolapitant's effects on preventing delayed PONV were explored up to 5 days after surgery.
A randomized, multicenter, double-blind, dose-ranging study of rolapitant was conducted with placebo and active control groups. Six hundred nineteen adult women undergoing open abdominal surgery were randomly assigned in equal ratios to 1 of 6 study arms: oral rolapitant in 5-mg, 20-mg, 70-mg, or 200-mg doses; IV ondansetron 4 mg; or placebo, stratified by history of PONV or motion sickness. The primary study endpoint was absence of emetic episodes, regardless of use of rescue medication, at 24 hours after extubation.
Groups assigned to rolapitant 20-mg, 70-mg, and 200-mg had a higher incidence of no emesis in comparison with placebo at 24 hours after surgery. A linear relationship between rolapitant dose and primary outcome was seen. The probability of an emetic episode was significantly lower in the rolapitant 70-mg and 200-mg groups in comparison with placebo (P ≤ 0.001 based on the log-rank test). No significant differences were noted between rolapitant and the active control (ondansetron) at 24 hours after surgery, but there was a higher incidence of no emesis (regardless of rescue medication use) in the rolapitant 200- and 70-mg groups at 72 and 120 hours, respectively.
Rolapitant is superior to placebo in reducing emetic episodes after surgery and reduces the incidence of vomiting in a dose-dependent manner. No differences in side effect profile were observed between rolapitant and placebo.
术后恶心和呕吐(PONV)是手术后常见的并发症。神经激肽-1(NK(1))受体拮抗剂已被证明在预防和治疗人类 PONV 方面是安全有效的。罗哌丁是一种有效的、选择性的 NK1 受体拮抗剂,吸收迅速,半衰期极长(长达 180 小时),并且似乎药物相互作用的潜力很低。我们评估了罗哌丁预防高危人群 PONV 的剂量反应,并探讨了罗哌丁对预防手术后 5 天内迟发性 PONV 的作用。
一项随机、多中心、双盲、剂量范围研究对罗哌丁进行了安慰剂和阳性对照的研究。619 名接受开腹手术的成年女性按比例随机分配至 6 个研究臂中的 1 个:口服罗哌丁 5mg、20mg、70mg 或 200mg 剂量;IV 昂丹司琼 4mg;或安慰剂,按 PONV 或运动病史分层。主要研究终点为拔管后 24 小时内无论是否使用解救药物,均无呕吐发作。
与安慰剂相比,接受罗哌丁 20mg、70mg 和 200mg 治疗的组在手术后 24 小时内的呕吐发生率更高。罗哌丁剂量与主要结局之间存在线性关系。与安慰剂相比,罗哌丁 70mg 和 200mg 组发生呕吐的概率显著降低(基于对数秩检验,P≤0.001)。与手术后 24 小时的阳性对照(昂丹司琼)相比,罗哌丁无显著差异,但在 72 小时和 120 小时,罗哌丁 200mg 和 70mg 组分别出现更多的无呕吐发作(无论是否使用解救药物)。
罗哌丁在减少手术后呕吐发作方面优于安慰剂,并呈剂量依赖性降低呕吐发生率。在副作用方面,罗哌丁与安慰剂无差异。