Worravitudomsuk Tarvit, Charuluxananan Somrat, Sukumpanumet Wasin, Sriprajittichai Pin
From the Department of Anesthesiology, Faculty of Medicine, Chulalongkorn University, King Chulalongkorn Memorial Hospital, Bangkok, Thailand.
Anesth Analg. 2025 Mar 1;140(3):628-635. doi: 10.1213/ANE.0000000000007091. Epub 2024 Oct 30.
Spinal anesthesia is the preferred anesthetic technique for cesarean deliveries. Postoperative nausea and vomiting (PONV) and pruritus occur in up to 80% and 83% of patients, respectively, after cesarean delivery with intrathecal opioids. Ondansetron is the recommended medication for PONV prophylaxis, but palonosetron, a second-generation 5-HT3 receptor antagonist, has a higher receptor affinity and a longer half-life. However, studies on palonosetron use in cesarean deliveries are limited. This study aimed to determine whether palonosetron was more effective than ondansetron in preventing intrathecal morphine-induced PONV and pruritus in cesarean deliveries.
Parturients who underwent cesarean delivery under spinal anesthesia were randomized into 3 groups: P (palonosetron 0.075 mg), O (ondansetron 4 mg), and N (normal saline). The study drug was intravenously administered after the umbilical cord was clamped. The primary outcome measures were the 48-hour incidence of PONV and pruritus. The secondary outcome measures were the PONV and pruritus scores at the postanesthesia care unit (PACU) and ward, rescue medications, satisfaction scores, and adverse events. Ordinal data were analyzed using the Kruskal-Wallis test. Continuous and categorical data were analyzed using a 1-way analysis of variance, Kruskal-Wallis test, and Pearson's χ 2 test, respectively. A value of P < .05 was considered significant. Post hoc analysis pairwise comparisons with Bonferroni correction were also performed.
Overall, 300 parturients were enrolled, and 297 parturients completed the study. One patient in the P group and 2 in the O group were excluded because of conversion to general anesthesia after failed spinal anesthesia. The baseline patient characteristics were comparable between the groups. The PONV incidence rates in the P, O, and N groups were 26.3% (95% confidence interval [CI], 17.4-35.1), 34.7% (95% CI, 25.1-44.3), and 50.0% (95% CI, 40.0-59.9), respectively ( P = .002). The incidence rates of pruritus in the P, O, and N groups were 69.7% (95% CI, 60.5-78.9), 76.5% (95% CI, 67.9-85.1), and 87.0% (95% CI, 80.3-93.7), respectively ( P = .013). Pairwise comparisons revealed significantly lower incidences of PONV and pruritus in the P group than in the N group ( P < .001 and P = .003, respectively). However, no significant differences were observed between the P and O groups or between the O and N groups. Additionally, the P group required significantly less nalbuphine rescue for pruritus than the N group ( P = .004 and P = .005 for the PACU and ward, respectively). PONV rescue, satisfaction scores, and adverse events were not significantly different among the 3 groups.
Palonosetron effectively prevents intrathecal morphine-induced PONV and pruritus during cesarean delivery. However, the efficacy of palonosetron is not significantly different from that of ondansetron.
脊髓麻醉是剖宫产的首选麻醉技术。剖宫产术中使用鞘内阿片类药物后,术后恶心呕吐(PONV)和瘙痒的发生率分别高达80%和83%。昂丹司琼是预防PONV的推荐药物,但第二代5 - HT3受体拮抗剂帕洛诺司琼具有更高的受体亲和力和更长的半衰期。然而,关于帕洛诺司琼在剖宫产中应用的研究有限。本研究旨在确定帕洛诺司琼在预防剖宫产中鞘内注射吗啡引起的PONV和瘙痒方面是否比昂丹司琼更有效。
接受脊髓麻醉下剖宫产的产妇被随机分为3组:P组(帕洛诺司琼0.075 mg)、O组(昂丹司琼4 mg)和N组(生理盐水)。研究药物在脐带结扎后静脉注射。主要观察指标为PONV和瘙痒的48小时发生率。次要观察指标为麻醉后恢复室(PACU)和病房的PONV和瘙痒评分、解救药物、满意度评分及不良事件。有序数据采用Kruskal - Wallis检验进行分析。连续数据和分类数据分别采用单因素方差分析、Kruskal - Wallis检验和Pearson卡方检验进行分析。P < 0.05被认为具有统计学意义。还进行了采用Bonferroni校正的事后分析两两比较。
总体而言,共纳入300名产妇,297名产妇完成研究。P组有1例患者、O组有2例患者因脊髓麻醉失败后转为全身麻醉而被排除。各组患者的基线特征具有可比性。P组、O组和N组的PONV发生率分别为26.3%(95%置信区间[CI],17.4 - 35.1)、34.7%(95% CI,25.1 - 44.3)和50.0%(95% CI,40.0 - 59.9)(P = 0.002)。P组、O组和N组的瘙痒发生率分别为69.7%(95% CI,60.5 - 78.9)、76.⑤%(95% CI,67.9 - 85.1)和87.0%(95% CI,80.3 - 93.7)(P = 0.013)。两两比较显示,P组的PONV和瘙痒发生率显著低于N组(分别为P < 0.001和P = 0.003)。然而,P组与O组之间或O组与N组之间未观察到显著差异。此外,P组因瘙痒所需的纳布啡解救量显著少于N组(PACU和病房分别为P = 0.004和P = 0.005)。3组之间的PONV解救、满意度评分及不良事件无显著差异。
帕洛诺司琼可有效预防剖宫产术中鞘内注射吗啡引起的PONV和瘙痒。然而,帕洛诺司琼的疗效与昂丹司琼无显著差异。