Department of Anesthesiology Xuanwu Hospital, Capital Medical University, No.45, Changchun Street, Beijing, 100053, China.
Department of Anesthesiology, Peking University International Hospital, Beijing, China.
BMC Anesthesiol. 2019 Jun 29;19(1):114. doi: 10.1186/s12871-019-0787-6.
BACKGROUND: Peripheral nerve block and local infiltration analgesia (LIA) provide good analgesia after knee replacement. This study evaluated the additional analgesic efficacy of continuous adductor canal block (ACB) added to single-dose LIA after medial unicondylar knee arthroplasty (UKA). We hypothesized ACB would lower pain scores and facilitate postoperative ambulation. METHODS: Forty-six patients were enrolled into this double-blind, randomized, placebo-controlled trial. UKA was performed and all patients received single-dose LIA intraoperatively. Patients were randomized into two groups: Group RP receiving 0.2% ropivacaine or Group Con receiving normal saline. A flow at 6 mL/h was administered for 48 h through a catheter in the adductor canal. Primary outcome was movement pain score at 24 h using the numeric rating scale (NRS-11). Secondary outcomes included serial postoperative pain scores, rate of patients with NRS>3 at rest and movement within 24 and 48 h postoperatively, time to breakthrough pain, quadriceps motor strength, ambulated distance, catheter related infection and patient satisfaction. RESULTS: Forty-two patients were analyzed. Pain scores with movement at 24 h postoperatively were significantly lower in Group RP than that in Group Con (3 vs. 5 NRS, P<0.001). Compared with Group Con, breakthrough pain occurred later in Group RP (18.5 vs 10.0 h, P = 0.002), serial pain scores at rest and with movement and rate of patients with NRS>3 with movement after surgery were significantly lower. Quadriceps motor strength was equivalent, however, ambulated distance on postoperative day 1 and 2 in Group Con was significant less (19.7 vs 37.3 m, P = 0.046; 33.4 vs 59.5 m, P = 0.002). CONCLUSIONS: Continuous adductor canal block added to single-dose LIA offered better analgesia and facilitated ambulation without motor weakness after medial UKA. TRIAL REGISTRATION: Clinical Trial Registration: ChiCTR-IOR-16008720 ; Registered 25 June 2016.
背景:外周神经阻滞和局部浸润镇痛(LIA)可提供膝关节置换术后良好的镇痛效果。本研究评估了内侧单髁膝关节置换术后(UKA)单次 LIA 中添加连续收肌管阻滞(ACB)的额外镇痛效果。我们假设 ACB 会降低疼痛评分并促进术后活动。
方法:本研究纳入了 46 名患者,采用双盲、随机、安慰剂对照试验。行 UKA 手术,所有患者术中接受单次 LIA。患者随机分为两组:RP 组给予 0.2%罗哌卡因,Con 组给予生理盐水。通过收肌管内的导管以 6ml/h 的流速输注 48 小时。主要结局是使用数字评分量表(NRS-11)在 24 小时时的运动疼痛评分。次要结局包括术后连续疼痛评分、术后 24 和 48 小时内休息和运动时 NRS>3 的患者比例、爆发痛出现时间、股四头肌运动力量、活动距离、导管相关感染和患者满意度。
结果:42 名患者纳入分析。术后 24 小时运动时疼痛评分在 RP 组明显低于 Con 组(3 分比 5 分,P<0.001)。与 Con 组相比,RP 组爆发痛出现时间较晚(18.5 小时比 10.0 小时,P=0.002),术后休息和运动时的连续疼痛评分以及运动时 NRS>3 的患者比例较低。股四头肌运动力量相当,但 Con 组术后第 1 天和第 2 天的活动距离明显减少(19.7 米比 37.3 米,P=0.046;33.4 米比 59.5 米,P=0.002)。
结论:在 UKA 术后单次 LIA 中添加连续收肌管阻滞可提供更好的镇痛效果,并促进活动,而不会导致股四头肌无力。
试验注册:临床试验注册:ChiCTR-IOR-16008720;注册日期:2016 年 6 月 25 日。
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