Ham Sung Yeon, Shim Yon Hee, Kim Eun Ho, Son Min Ji, Park Won Sun, Lee Jeong Soo
From the Department of Anaesthesiology and Pain Medicine, Yonsei University College of Medicine (SYH, EHK), Department of Anaesthesiology and Pain Medicine, Anaesthesia and Pain Research Institute, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea (YHS, JSL), Department of Biology, Johns Hopkins University, Baltimore, Maryland, USA (MJS), and Department of Anaesthesiology and Pain Medicine, Anaesthesia and Pain Research Institute, Yongin Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea (WSP).
Eur J Anaesthesiol. 2016 Feb;33(2):90-5. doi: 10.1097/EJA.0000000000000242.
Ondansetron, a 5-HT3 receptor antagonist, and aprepitant, a neurokinin-1 receptor antagonist, block the emetic effect of serotonin and neurokinin, respectively. Aprepitant combined with ondansetron can be more effective for preventing emesis in patients at high risk of postoperative nausea and vomiting (PONV).
To investigate the prophylactic effect of combining aprepitant with ondansetron compared with ondansetron alone on PONV in patients with fentanyl-based patient-controlled analgesia (PCA) after laparoscopic gynaecological surgery.
Single-centre, double-blinded randomised controlled trial.
A major university hospital in Seoul, Korea, between July 2012 and April 2013.
One hundred and twenty-five female patients (American Society of Anesthesiologists' physical status 1 or 2) with fentanyl-based intravenous PCA after gynaecological laparoscopy were recruited to the study, and 110 completed the protocol.
Oral aprepitant 80 mg or placebo was given 1 h before anaesthesia. In all patients, ondansetron 4 mg was administered intravenously at the end of surgery and 12 mg was added to the PCA solution.
The primary outcome measure was complete response (no PONV and no rescue antiemetics) up to 48 h postoperatively.
There was no difference in the proportion of complete responses to 48 h between the groups (P = 0.05), but in the post-anaesthesia care unit and up to 24 h postoperatively, the proportion was significantly higher in the aprepitant and ondansetron group than in the ondansetron only group (76 vs. 50%, P = 0.004 and 38 vs. 16%, P = 0.011, respectively). In the aprepitant and ondansetron group, the time to first PONV was delayed (P = 0.014) and the incidence of nausea up to 24 h postoperatively was lower (P = 0.014). However, there were no differences in the incidences of retching or vomiting, the severity of nausea, use of rescue antiemetics or the incidence of side-effects.
Aprepitant 80 mg orally with ondansetron is effective in suppressing early PONV up to 24 h postoperatively and delays the time to first PONV in patients with fentanyl-based intravenous PCA after gynaecological laparoscopy. However, the combination prophylaxis with aprepitant and ondansetron failed to reach the predefined primary study outcome when compared with ondansetron alone.
Clinicaltrial.gov identifier: NCT01897337.
昂丹司琼是一种5-羟色胺3(5-HT3)受体拮抗剂,阿瑞匹坦是一种神经激肽-1(NK-1)受体拮抗剂,分别可阻断血清素和神经激肽的催吐作用。阿瑞匹坦联合昂丹司琼对预防术后恶心呕吐(PONV)高风险患者的呕吐可能更有效。
探讨与单用昂丹司琼相比,阿瑞匹坦联合昂丹司琼对接受腹腔镜妇科手术后使用芬太尼自控镇痛(PCA)患者PONV的预防效果。
单中心、双盲随机对照试验。
2012年7月至2013年4月期间,韩国首尔的一所大型大学医院。
125例妇科腹腔镜检查后接受芬太尼静脉PCA的女性患者(美国麻醉医师协会身体状况分级为1或2级)被纳入研究,110例完成试验方案。
麻醉前1小时口服80毫克阿瑞匹坦或安慰剂。所有患者在手术结束时静脉注射4毫克昂丹司琼,并在PCA溶液中添加12毫克。
主要观察指标为术后48小时内的完全缓解(无PONV且未使用补救性止吐药)。
两组至术后48小时完全缓解的比例无差异(P = 0.05),但在麻醉后护理单元及术后24小时内,阿瑞匹坦和昂丹司琼联合组的比例显著高于单用昂丹司琼组(分别为76%对50%,P = 0.004;38%对16%,P = 0.011)。在阿瑞匹坦和昂丹司琼联合组中,首次发生PONV的时间延迟(P = 0.014),术后24小时内恶心的发生率较低(P = 0.014)。然而,干呕或呕吐的发生率、恶心的严重程度、补救性止吐药的使用或副作用的发生率并无差异。
口服80毫克阿瑞匹坦联合昂丹司琼可有效抑制妇科腹腔镜检查后使用芬太尼静脉PCA患者术后24小时内的早期PONV,并延迟首次PONV的发生时间。然而,与单用昂丹司琼相比,阿瑞匹坦和昂丹司琼联合预防未能达到预先定义的主要研究结果。
Clinicaltrial.gov标识符:NCT01897337。