Anesthesiology, Showa University, Tokyo, Japan
Anesthesiology, Showa University, Tokyo, Japan.
Reg Anesth Pain Med. 2019 Jun;44(6):632-636. doi: 10.1136/rapm-2018-100091. Epub 2019 Apr 3.
Lumbar plexus block (LPB) is an effective perioperative analgesic therapy for patients undergoing total hip arthroplasty (THA). However, the analgesic efficacy of intermittent administration compared with continuous infusion of LPB in patients remains unclear.
Forty adult patients who underwent THA were randomly divided into two groups: continuous infusion group (6 mL/hour continuous infusion of levobupivacaine [0.125%] in LPB, n=20) and intermittent infusion group (12 mL of levobupivacaine [0.125%] bolus delivered every 2 hours in LPB, n=20). The primary outcome was the cumulative fentanyl consumption administered for rescue analgesia during the first 48 hours after surgery. Secondary outcomes were the number of demands for rescue analgesia and successfully delivered rescue analgesia; extent of sensory blockade (cold tests); and pain score on the visual analog scale (VAS) at rest and during mobilization during the first 48 hours after surgery.
Both the cumulative fentanyl consumption administered for rescue analgesia (mean [SD]: 81.5 [58.5] μg vs 438 [101.2] μg among the intermittent infusion and the continuous infusion groups, respectively) and the number of demanded and delivered fentanyl boluses for rescue analgesia were lower in intermittent infusion group than in continuous infusion (p<0.001 for both). The extent of sensory blockade remained constant in intermittent infusion group, but gradually narrowed in continuous infusion. VAS was lower in intermittent infusion group than in continuous infusion, except at 1 and 12 hours postoperatively (p<0.05).
Greater analgesic effect was achieved using the intermittent mode than the continuous mode of LPB administration.
腰椎丛阻滞(LPB)是全髋关节置换术(THA)患者有效的围手术期镇痛治疗方法。然而,LPB 间歇性给药与连续输注在患者中的镇痛效果尚不清楚。
40 名接受 THA 的成年患者被随机分为两组:连续输注组(LPB 中以 6ml/小时的速度持续输注布比卡因[0.125%],n=20)和间歇输注组(LPB 中每 2 小时给予 12ml 布比卡因[0.125%]推注,n=20)。主要结局是术后 48 小时内用于解救镇痛的累积芬太尼消耗量。次要结局是解救镇痛的需求次数和成功给予解救镇痛的次数;感觉阻滞程度(冷试验);以及术后 48 小时内休息和活动时的视觉模拟评分(VAS)疼痛评分。
间歇输注组用于解救镇痛的累积芬太尼消耗量([均值(SD)]:81.5[58.5]μg vs 连续输注组的 438[101.2]μg)和用于解救镇痛的芬太尼推注需求次数和实际给予次数均低于连续输注组(均 p<0.001)。间歇输注组的感觉阻滞程度保持不变,但连续输注组逐渐变窄。间歇输注组的 VAS 低于连续输注组,除术后 1 小时和 12 小时外(p<0.05)。
与 LPB 连续输注模式相比,间歇输注模式具有更强的镇痛效果。