University of Connecticut School of Medicine, 263 Farmington Avenue, Farmington, CT 06032.
J Bone Joint Surg Am. 2013 Nov 6;95(21):1935-41. doi: 10.2106/JBJS.L.00477.
We studied the efficacy of local infiltration analgesia in surgical wounds with 0.2% ropivacaine (50 mL), ketorolac (15 mg), and adrenaline (0.5 mg) compared with that of local infiltration analgesia combined with continuous infusion of 0.2% ropivacaine as a method of pain control after total hip arthroplasty. We hypothesized that as a component of multimodal analgesia, local infiltration analgesia followed by continuous infusion of ropivacaine would result in reduced postoperative opioid consumption and lower pain scores compared with infiltration alone, and that both of these techniques would be superior to placebo.
In this prospective, double-blind, placebo-controlled study, 105 patients were randomized into three groups: Group I, in which patients received infiltration with ropivacaine, ketorolac, and adrenaline followed by continuous infusion of 0.2% ropivacaine at 5 mL/hr; Group II, in which patients received infiltration with ropivacaine, ketorolac, and adrenaline followed by continuous infusion of saline solution at 5 mL/hr; and Group III, in which patients received infiltration with saline solution followed by continuous infusion of saline solution at 5 mL/hr.All patients received celecoxib, pregabalin, and acetaminophen perioperatively and patient-controlled analgesia; surgery was performed under general anesthesia. Before wound closure, the tissues and periarticular space were infiltrated with ropivacaine, ketorolac, and adrenaline or saline solution and a fenestrated catheter was placed. The catheter was attached to a pump prefilled with either 0.2% ropivacaine or saline solution set to infuse at 5 mL/hr.The primary outcome measure was postoperative opioid consumption and the secondary outcome measures were pain scores, adverse side effects, and patient satisfaction.
There were no differences between groups in the administration of opioids in the operating room, in the recovery room, or on the surgical floor. The pain scores on recovery room admission and discharge and the floor were low and similar between groups. There were no differences in the incidence of adverse side effects among groups. Patient satisfaction with pain management was similar in all groups.
Local infiltration analgesia alone or followed by continuous infusion of ropivacaine as part of multimodal analgesia provides no additional analgesic benefit or reduction in opioid consumption compared with placebo following total hip arthroplasty.
Therapeutic level I. See Instructions for Authors for a complete description of levels of evidence.
我们研究了在手术伤口中使用 0.2%罗哌卡因(50 毫升)、酮咯酸(15 毫克)和肾上腺素(0.5 毫克)进行局部浸润镇痛的效果,与局部浸润镇痛联合 0.2%罗哌卡因持续输注相比,作为全髋关节置换术后疼痛控制的一种方法。我们假设,作为多模式镇痛的一部分,局部浸润镇痛加用罗哌卡因持续输注将导致术后阿片类药物消耗减少和疼痛评分降低,与单纯浸润相比,这两种方法都优于安慰剂。
在这项前瞻性、双盲、安慰剂对照研究中,105 名患者随机分为三组:I 组患者接受罗哌卡因、酮咯酸和肾上腺素浸润,然后以 5 毫升/小时的速度持续输注 0.2%罗哌卡因;II 组患者接受罗哌卡因、酮咯酸和肾上腺素浸润,然后以 5 毫升/小时的速度持续输注生理盐水;III 组患者接受生理盐水浸润,然后以 5 毫升/小时的速度持续输注生理盐水。所有患者均接受塞来昔布、普瑞巴林和对乙酰氨基酚围手术期治疗和患者自控镇痛;手术均在全身麻醉下进行。在伤口关闭前,用罗哌卡因、酮咯酸和肾上腺素或生理盐水对组织和关节周围间隙进行浸润,并放置一个带孔的导管。导管连接到一个预先填充有 0.2%罗哌卡因或生理盐水的泵上,设定以 5 毫升/小时的速度输注。主要观察指标为术后阿片类药物的使用情况,次要观察指标为疼痛评分、不良反应和患者满意度。
三组患者在手术室、恢复室和手术楼层的阿片类药物使用无差异。恢复室入院、出院和楼层的疼痛评分较低且相似。三组不良反应发生率无差异。各组患者对疼痛管理的满意度相似。
与安慰剂相比,单纯局部浸润镇痛或作为多模式镇痛的一部分联合罗哌卡因持续输注在全髋关节置换术后并未提供额外的镇痛益处或减少阿片类药物的消耗。
治疗水平 I. 请参阅作者说明以获取完整的证据水平描述。