Yoo Jae Hwa, Jeon In Suk, Chung Ji Won, Ryoo Jae Hoon, You Gyu Wan, Kim Soon Im
Department of Anesthesiology and Pain Medicine, Soonchunhyang University Seoul Hospital, Seoul, Korea.
Department of Anesthesiology and Pain Medicine, Soonchunhyang University Gumi Hospital, Gumi, Korea.
Anesth Pain Med (Seoul). 2020 Jan 31;15(1):28-34. doi: 10.17085/apm.2020.15.1.28.
We compared the effects of palonosetron with ondansetron for preventing postoperative nausea and vomiting (PONV) during the first 24 h after surgery in women receiving intravenous patient-controlled analgesia (IV-PCA) with fentanyl for pain control.
In this prospective, randomized, double-blinded study, 204 healthy patients who were undergoing elective surgery with general anesthesia were enrolled. In the palonosetron group (n = 102), 0.075 mg bolus was given intravenously (i.v.) 30 min before the end of surgery and 8 ml saline was added to the IV-PCA. In the ondansetron group (n = 102), 8 mg bolus i.v. was given 30 min before the end of surgery and 16 mg of ondansetron was added to the IV-PCA. The incidence of PONV, severity of nausea, and use of rescue anti-emetics were evaluated 6 and 24 h after the operation.
The incidences of nausea (55.6%) and vomiting (14.1%) in the palonosetron group did not differ from those (58.3 and 19.8%) in the ondansetron group during the first 24 h after surgery (P > 0.05). No significant differences were observed in the severity of nausea and use of rescue anti-emetics between the two groups (P > 0.05).
The effects of palonosetron in preventing PONV were not different from those of ondansetron during the first 24 h postoperatively in women receiving IV-PCA with fentanyl.
我们比较了帕洛诺司琼与昂丹司琼在接受静脉自控镇痛(IV-PCA)联合芬太尼控制疼痛的女性患者术后24小时内预防术后恶心呕吐(PONV)的效果。
在这项前瞻性、随机、双盲研究中,纳入了204例接受全身麻醉择期手术的健康患者。在帕洛诺司琼组(n = 102)中,在手术结束前30分钟静脉注射(i.v.)0.075 mg推注剂量,并在IV-PCA中加入8 ml生理盐水。在昂丹司琼组(n = 102)中,在手术结束前30分钟静脉注射8 mg推注剂量,并在IV-PCA中加入16 mg昂丹司琼。在术后6小时和24小时评估PONV的发生率、恶心的严重程度以及急救止吐药的使用情况。
术后24小时内,帕洛诺司琼组恶心(55.6%)和呕吐(14.1%)的发生率与昂丹司琼组(58.3%和19.8%)无差异(P > 0.05)。两组之间恶心的严重程度和急救止吐药的使用情况无显著差异(P > 0.05)。
在接受芬太尼IV-PCA的女性患者术后24小时内,帕洛诺司琼预防PONV的效果与昂丹司琼无差异。