O'Donnell Brian D, Ryan Helen, O'Sullivan Owen, Iohom Gabrielle
Department of Anesthesia, Cork University Hospital, Wilton Rd., Cork, Ireland.
Anesth Analg. 2009 Jul;109(1):279-83. doi: 10.1213/ane.0b013e3181a3e721.
We performed a randomized, controlled trial comparing low-dose ultrasound-guided axillary block with general anesthesia evaluating anesthetic and perioperative analgesic outcomes.
Patients were randomized to either ultrasound-guided axillary block or general anesthesia. Ultrasound-guided axillary block was performed using a needle-out-of-plane approach. Up to 5 mL of local anesthetic injectate (equal parts 2% lidocaine with 1:200,000 epinephrine and 0.5% bupivacaine with 7.5 mg/mL clonidine) was injected after identifying the median, ulnar, radial, and musculocutaneous nerves. A maximum of 20 mL local anesthetic injectate was used. General anesthesia was standardized to include induction with fentanyl and propofol, maintenance with sevoflurane in an oxygen/nitrous oxide mixture. Pain scores were measured in the recovery room and at 2, 6, 24, 48 h, and 7 days. Ability to bypass the recovery room and time to achieve hospital discharge criteria were also assessed.
All ultrasound-guided axillary block patients achieved satisfactory anesthesia. The ultrasound-guided axillary block group had lower visual analog scale pain scores in the recovery room (0.3 [1.3] vs 55.8 [36.5], P < 0.001), and visual rating scale pain scores at 2 h (0.3 [1.3] vs 45 [29.6], P < 0.001), and at 6 h (1.1 [2.7] vs 4 [2.8], P < 0.01). All ultrasound-guided axillary block patients bypassed the recovery room and attained earlier hospital discharge criteria (30 min vs 120 min 30/240 P < 0.0001 median [range]).
Ultrasound-guided axillary brachial plexus block with 20 mL local anesthetic mixture provided satisfactory anesthesia and superior analgesia after upper limb trauma surgery when compared with general anesthesia.
我们进行了一项随机对照试验,比较低剂量超声引导下腋路阻滞与全身麻醉,并评估麻醉和围手术期镇痛效果。
患者被随机分为超声引导下腋路阻滞组或全身麻醉组。超声引导下腋路阻滞采用平面外进针方法。在识别正中神经、尺神经、桡神经和肌皮神经后,注射最多5毫升局部麻醉剂注射液(2%利多卡因与1:200,000肾上腺素等份混合,以及0.5%布比卡因与7.5毫克/毫升可乐定)。最多使用20毫升局部麻醉剂注射液。全身麻醉标准化为包括用芬太尼和丙泊酚诱导、在氧气/氧化亚氮混合气体中用七氟醚维持。在恢复室以及术后2、6、24、48小时和7天测量疼痛评分。还评估了绕过恢复室的能力和达到出院标准的时间。
所有超声引导下腋路阻滞患者均获得了满意的麻醉效果。超声引导下腋路阻滞组在恢复室的视觉模拟评分疼痛得分较低(0.3 [1.3] 对比55.8 [36.5],P < 0.001),在2小时时的视觉评分量表疼痛得分较低(0.3 [1.3] 对比45 [29.6],P < 0.001),以及在6小时时的视觉评分量表疼痛得分较低(1.1 [2.7] 对比4 [2.8],P < 0.01)。所有超声引导下腋路阻滞患者都绕过了恢复室,并更早达到出院标准(30分钟对比120分钟 30/240 P < 0.0001中位数[范围])。
与全身麻醉相比,采用20毫升局部麻醉剂混合物的超声引导下腋路臂丛神经阻滞在上肢创伤手术后提供了满意的麻醉效果和更好的镇痛效果。