Ittichaikulthol Wichai, Prachanpanich Naruemol, Kositchaiwat Chutima, Intapan Theerayut
Department of Anesthesiology, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
J Med Assoc Thai. 2010 Aug;93(8):937-42.
Nonsteroidal antiinflammatory drugs (NSAIDs) in combination with opioids is a model of multimodal analgesia. NSAIDs have the oral and parenteral forms.
The aim of the present study was to evaluate the efficacy of celecoxib compared with placebo and parecoxib after total hip or knee arthroplasty.
A total of 120, ASA 1-2, aged 18-75 years, patients were randomly assigned to receive one of the three groups: Group I (control) received placebo (n=40), group II received 400 mg celecoxib orally (n=40) and group III received 40 mg parecoxib intravenously (n=40). The present study medication was administered I hour before surgery. All patients had access to patient-controlled analgesia (PCA) with intravenous morphine. Patients were studied at 0, 1, 6, 12 and 24 hours postoperatively for verbal numerical rating scale (VNRS), morphine consumption, satisfaction score and side effects.
The intraoperatively fentayl requirement were similar among the three groups (p < 0.00). Celecoxib and parecoxib significantly decreased the amount of morphine requirement after total hip or knee arthroplasty compared to placebo at 1, 6, 12 and 24 hours (p < 0.00). The celecoxib group required more morphine than the parecoxib group at 1, 6, 12 and 24 hours (p < 0.00). The VNRS score in parecoxib group was significantly lower than the celecoxib and control groups at 1, 6, 12 but not at 24 hours. The VNRS score was lower in the celecoxib group compared to the control group at I and 6 hours postoperatively (p = 0.01, p < 0. 01 respectively). The placebo group had a higher sedation score (p = 0.008) but not for nausea vomiting (p = 0.36) and pruritus (p = 0.12) compared to the treatment groups.
Within 12 hours after total hip and knee arthroplasty, pre-operative administration of parenteral parecoxib 40 mg was more effective than oral celecoxib 400 mg and placebo in terms of morphine consumption and VNRS score.
非甾体抗炎药(NSAIDs)与阿片类药物联合使用是一种多模式镇痛的模式。NSAIDs有口服和肠胃外给药两种形式。
本研究的目的是评估塞来昔布与安慰剂及帕瑞昔布在全髋关节或膝关节置换术后的疗效。
总共120例年龄在18 - 75岁、ASA分级为1 - 2级的患者被随机分配到三组中的一组:第一组(对照组)接受安慰剂(n = 40),第二组口服400 mg塞来昔布(n = 40),第三组静脉注射40 mg帕瑞昔布(n = 40)。本研究药物在手术前1小时给药。所有患者均可使用静脉注射吗啡的患者自控镇痛(PCA)。在术后0、1、6、12和24小时对患者进行言语数字评定量表(VNRS)、吗啡用量、满意度评分及副作用的研究。
三组术中芬太尼需求量相似(p < 0.00)。与安慰剂相比,塞来昔布和帕瑞昔布在全髋关节或膝关节置换术后1、6、12和24小时显著降低了吗啡需求量(p < 0.00)。在1、6、12和24小时,塞来昔布组比帕瑞昔布组需要更多的吗啡(p < 0.00)。帕瑞昔布组在1、6、12小时的VNRS评分显著低于塞来昔布组和对照组,但在24小时时并非如此。塞来昔布组在术后1小时和6小时的VNRS评分低于对照组(分别为p = 0.01,p < 0.01)。与治疗组相比,安慰剂组的镇静评分更高(p = 0.008),但恶心呕吐(p = 0.36)和瘙痒(p = 0.12)方面则不然。
在全髋关节和膝关节置换术后12小时内,术前静脉注射40 mg帕瑞昔布在吗啡用量和VNRS评分方面比口服400 mg塞来昔布和安慰剂更有效。