Schwenk Eric S, Gandhi Kishor, Baratta Jaime L, Torjman Marc, Epstein Richard H, Chung Jaeyoon, Vaghari Benjamin A, Beausang David, Bojaxhi Elird, Grady Bernadette
Department of Anesthesiology, Thomas Jefferson University Hospital, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, USA.
Princeton University Medical Center, Princeton University, Plainsboro Township, USA.
Anesth Pain Med. 2015 Dec 5;5(6):e31111. doi: 10.5812/aapm.31111. eCollection 2015 Dec.
Continuous interscalene blocks provide excellent analgesia after shoulder surgery. Although the safety of the ultrasound-guided in-plane approach has been touted, technical and patient factors can limit this approach. We developed a caudad-to-cephalad out-of-plane approach and hypothesized that it would decrease pain ratings due to better catheter alignment with the brachial plexus compared to the in-plane technique in a randomized, controlled study.
To compare an out-of-plane interscalene catheter technique to the in-plane technique in a randomized clinical trial.
Eighty-four patients undergoing open shoulder surgery were randomized to either the in-plane or out-of-plane ultrasound-guided continuous interscalene technique. The primary outcome was VAS pain rating at 24 hours. Secondary outcomes included pain ratings in the recovery room and at 48 hours, morphine consumption, the incidence of catheter dislodgments, procedure time, and block difficulty. Procedural data and all pain ratings were collected by blinded observers.
There were no differences in the primary outcome of median VAS pain rating at 24 hours between the out-of-plane and in-plane groups (1.50; IQR, [0 - 4.38] vs. 1.25; IQR, [0 - 3.75]; P = 0.57). There were also no differences, respectively, between out-of-plane and in-plane median PACU pain ratings (1.0; IQR, [0 - 3.5] vs. 0.25; IQR, [0 - 2.5]; P = 0.08) and median 48-hour pain ratings (1.25; IQR, [1.25 - 2.63] vs. 0.50; IQR, [0 - 1.88]; P = 0.30). There were no differences in any other secondary endpoint.
Our out-of-plane technique did not provide superior analgesia to the in-plane technique. It did not increase the number of complications. Our technique is an acceptable alternative in situations where the in-plane technique is difficult to perform.
连续肌间沟阻滞可为肩部手术后提供出色的镇痛效果。尽管超声引导平面内穿刺法的安全性已得到广泛认可,但技术因素和患者因素可能会限制该方法的应用。我们开发了一种尾端至头端的平面外穿刺法,并假设在一项随机对照研究中,与平面内技术相比,该方法能使导管与臂丛神经的对齐更好,从而降低疼痛评分。
在一项随机临床试验中,比较平面外肌间沟导管技术与平面内技术。
84例接受开放性肩部手术的患者被随机分为平面内或平面外超声引导下连续肌间沟技术组。主要结局指标为术后24小时的视觉模拟评分(VAS)疼痛评分。次要结局指标包括恢复室和术后48小时的疼痛评分、吗啡用量、导管移位发生率、操作时间及阻滞难度。操作数据和所有疼痛评分均由不知情的观察者收集。
平面外组与平面内组术后24小时VAS疼痛评分中位数这一主要结局指标无差异(1.50;四分位间距,[0 - 4.38] 对比 1.25;四分位间距,[0 - 3.75];P = 0.57)。平面外组与平面内组术后麻醉恢复室(PACU)疼痛评分中位数(1.0;四分位间距,[0 - 3.5] 对比 0.25;四分位间距,[0 - 2.5];P = 0.08)以及术后48小时疼痛评分中位数(1.25;四分位间距,[1.25 - 2.63] 对比 0.50;四分位间距,[0 - 1.88];P = 0.30)也均无差异。其他次要终点指标也无差异。
我们的平面外技术并未比平面内技术提供更优的镇痛效果,也未增加并发症的数量。在平面内技术难以实施的情况下,我们的技术是一种可接受的替代方法。