Pinsornsak Piya, Teeyaphudit Mungkorn, Ruetiwarangkoon Chaivet, Chaiwuttisak Adisai
Department of Orthopaedic Surgery, Thammasat University, Khlong Luang, Pathum Thani, Thailand.
J Arthroplasty. 2017 Mar;32(3):1040-1043. doi: 10.1016/j.arth.2016.09.013. Epub 2016 Oct 8.
Spinal anesthesia with intrathecal morphine is a reliable, easy to apply, and cost effective method for controlling pain after total knee arthroplasty (TKA). However, postoperative nausea and vomiting (PONV) is a major concern. 5-Hydroxytryptamine receptor 3 (5-HT) antagonists like ondansetron and ramosetron are commonly used for preventing PONV, but the optimal choice remains unclear. We conducted a study to assess the effectiveness of ramosetron and ondansetron, hypothesizing that the longer acting ramosetron may be better than ondansetron in the first 48 hours after TKA, performed with spinal anesthesia and intrathecal morphine.
Patients were randomized preoperatively to either intravenous ondansetron (8 mg) or ramosetron (0.3 mg). The primary outcomes were the incidence rates of PONV. Secondary outcomes were the need for a rescue antiemetic (metoclopramide), pain score, patient satisfaction, and adverse drug reactions (ADRs) at 0-6, 6-12, 12-24, and 24-48 hours.
Ninety patients were evaluable; 45 patients/arm. Compared with ondansetron, ramosetron was associated with significantly lower incidence rates of nausea at: (1) 12-18 hours: 3/45 vs 11/45 (P = .016), (2) 18-24 hours: 1/45 vs 9/45 (P = .005), and vomiting at 18-24 hours: 1/45 vs 6/45 (P = .044). There were no significant differences in the use of rescue-antiemetic medicine, pain score, patient satisfaction, and ADRs.
Preoperative ramosetron provided more prolonged PONV prophylaxis than ondansetron after TKA in our setting, and had a similar ADR profile. Other trials are needed to confirm our results before ramosetron is adopted widely.
鞘内注射吗啡的脊髓麻醉是全膝关节置换术(TKA)后控制疼痛的一种可靠、易于实施且具有成本效益的方法。然而,术后恶心呕吐(PONV)是一个主要问题。5-羟色胺受体3(5-HT)拮抗剂如昂丹司琼和雷莫司琼常用于预防PONV,但最佳选择仍不明确。我们进行了一项研究以评估雷莫司琼和昂丹司琼的有效性,假设在TKA后最初48小时内,作用时间更长的雷莫司琼可能比昂丹司琼更好,该研究采用脊髓麻醉和鞘内注射吗啡。
患者在术前随机分为静脉注射昂丹司琼(8毫克)或雷莫司琼(0.3毫克)两组。主要结局是PONV的发生率。次要结局是在0 - 6、6 - 12、12 - 24和24 - 48小时时使用补救性止吐药(甲氧氯普胺)的必要性、疼痛评分、患者满意度和药物不良反应(ADR)。
90例患者可进行评估;每组45例患者。与昂丹司琼相比,雷莫司琼在以下时间点与显著更低的恶心发生率相关:(1)12 - 18小时:3/45 vs 11/45(P = .016),(2)18 - 24小时:1/45 vs 9/45(P = .005),以及在18 - 24小时时呕吐发生率:1/45 vs 6/45(P = .044)。在使用补救性止吐药、疼痛评分、患者满意度和ADR方面无显著差异。
在我们的研究中,术前使用雷莫司琼比昂丹司琼在TKA后提供了更持久的PONV预防,且药物不良反应情况相似。在雷莫司琼被广泛采用之前,还需要其他试验来证实我们的结果。