Szarvas Szilvia, Chellapuri Ramesh S, Harmon Dominic C, Owens John, Murphy Damian, Shorten George D
Department of Anesthesia and Intensive Care Medicine, Cork University Hospital and University College Cork, Ireland.
Anesth Analg. 2003 Jul;97(1):259-63, table of contents. doi: 10.1213/01.ane.0000066310.49139.2a.
In a prospective, double-blinded, randomized trial, we evaluated the efficacy of IV (a) dexamethasone 8 mg, (b) ondansetron 8 mg, and (c) dexamethasone 8 mg plus ondansetron 4 mg for the prevention of postoperative nausea, vomiting (PONV), and pruritus in 130 (ASA physical status I to III) patients undergoing elective major orthopedic surgery after spinal anesthesia with hyperbaric 0.5% bupivacaine and intrathecal morphine. After spinal anesthesia, patients were randomized to one of three groups. Failure of PONV prophylaxis in the 24-h postoperative period occurred more frequently in patients who received dexamethasone alone (29 of 40; 73%) compared with those who received either ondansetron alone (23 of 47; 49%) (P = 0.02) or dexamethasone plus ondansetron together (19 of 43; 44%)(P = 0.01). There was no difference in the incidence of failure of prophylaxis of pruritus (70%, 72%, and 70% in dexamethasone 8 mg, ondansetron 8 mg, and dexamethasone 8 mg plus ondansetron 4 mg, respectively) (P > 0.1) in the 24-h postoperative period. We conclude that the administration of dexamethasone 8 mg with ondansetron 4 mg has no added benefit compared with ondansetron 8 mg alone in the prophylaxis of PONV and pruritus.
Postoperative nausea and vomiting (PONV) and pruritus are common side effects after spinal opioid administration. In this study, dexamethasone 8 mg plus ondansetron 4 mg was as effective as ondansetron 8 mg. The administration of dexamethasone alone was associated with a frequent incidence of PONV, demonstrating a lack of efficacy. This has important cost implications.
在一项前瞻性、双盲、随机试验中,我们评估了静脉注射(a)8毫克地塞米松、(b)8毫克昂丹司琼以及(c)8毫克地塞米松加4毫克昂丹司琼对130例(美国麻醉医师协会身体状况分级为I至III级)接受0.5%重比重布比卡因脊髓麻醉和鞘内注射吗啡的择期大型骨科手术患者术后恶心、呕吐(PONV)及瘙痒的预防效果。脊髓麻醉后,患者被随机分为三组。术后24小时内,单独接受地塞米松治疗的患者PONV预防失败的发生率(40例中的29例;73%)高于单独接受昂丹司琼治疗的患者(47例中的23例;49%)(P = 0.02)或接受地塞米松加昂丹司琼联合治疗的患者(43例中的19例;44%)(P = 0.01)。术后24小时内,瘙痒预防失败的发生率在8毫克地塞米松组、8毫克昂丹司琼组和8毫克地塞米松加4毫克昂丹司琼组中分别为70%、72%和70%,差异无统计学意义(P > 0.1)。我们得出结论,在预防PONV和瘙痒方面,8毫克地塞米松与4毫克昂丹司琼联合使用相比单独使用8毫克昂丹司琼并无额外益处。
术后恶心呕吐(PONV)和瘙痒是脊髓给予阿片类药物后的常见副作用。在本研究中,8毫克地塞米松加4毫克昂丹司琼与8毫克昂丹司琼效果相同。单独使用地塞米松与PONV的高发生率相关,表明其缺乏疗效。这具有重要的成本意义。