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锁骨下臂丛神经阻滞用于下臂的区域麻醉。

Infraclavicular brachial plexus block for regional anaesthesia of the lower arm.

作者信息

Chin Ki Jinn, Alakkad Husni, Adhikary Sanjib D, Singh Mandeep

机构信息

Department of Anesthesia, University of Toronto, Toronto Western Hospital, 399 Bathurst Street, Toronto, Ontario, Canada, M5T 2S8.

出版信息

Cochrane Database Syst Rev. 2013 Aug 28;2013(8):CD005487. doi: 10.1002/14651858.CD005487.pub3.

DOI:10.1002/14651858.CD005487.pub3
PMID:23986434
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11666099/
Abstract

BACKGROUND

Several approaches exist to produce local anaesthetic blockade of the brachial plexus. It is not clear which is the technique of choice for providing surgical anaesthesia of the lower arm, although infraclavicular blockade (ICB) has several purported advantages. We therefore performed a systematic review of ICB compared to the other brachial plexus blocks (BPBs). This review was originally published in 2010 and was updated in 2013.

OBJECTIVES

The objective of this review was to evaluate the efficacy and safety of infraclavicular block (ICB) compared to other approaches to the brachial plexus in providing regional anaesthesia for surgery on the lower arm.

SEARCH METHODS

We searched the Cochrane Central Register of Controlled Trials (CENTRAL) in The Cochrane Library (2013, Issue 5); MEDLINE (1966 to June 2013) via OvidSP; and EMBASE (1980 to June 2013) via OvidSP. We also searched conference proceedings (from 2004 to 2012) and the www.clinicaltrials.gov trials registry. The searches for the original review were performed in September 2008.

SELECTION CRITERIA

We included any randomized controlled trials (RCTs) that compared ICB with other BPBs as the sole anaesthetic technique for surgery on the lower arm.

DATA COLLECTION AND ANALYSIS

The primary outcome was adequate surgical anaesthesia within 30 minutes of block completion. Secondary outcomes included sensory block of individual nerves, tourniquet pain, onset time of sensory blockade, block performance time, block-associated pain and complications related to the block.

MAIN RESULTS

In our original review we included 15 studies with 1020 participants and excluded two. In this updated review we included seven new studies and excluded six, bringing the total number of included studies to 22 and involving 1732 participants. The control group intervention was the axillary block in 14 studies, supraclavicular block in six studies, mid-humeral block in two studies, and parascalene block in one study. One study compared ICB to both axillary and supraclavicular blocks. Nine studies employed ultrasound-guided ICB. The risk of failed surgical anaesthesia 30 minutes after block completion was similar for ICB and all other BPBs (11.4% versus 12.9%, risk ratio (RR) 0.88, 95% CI 0.51 to 1.52, P = 0.64), but tourniquet pain was less likely with ICB (11.9% versus 18.0%; RR of experiencing tourniquet pain 0.66, 95% CI 0.47 to 0.92, P = 0.02). Subgroup analysis by method of nerve localization, and by control group intervention, did not show any statistically significant differences in the risk of failed surgical anaesthesia. However when compared to a single-injection axillary block, ICB was better at providing complete sensory block of the musculocutaneous nerve (RR for failure 0.46, 95% CI 0.27 to 0.60, P < 0.0001). ICB had a slightly longer sensory block onset time (mean difference (MD) 1.9 min, 95% CI 0.2 to 3.6, P = 0.03) but was faster to perform than multiple-injection axillary (MD -2.7 min, 95% CI -3.4 to -2.0, P < 0.00001) or mid-humeral (MD -4.8 min, 95% CI -6.0 to -3.6, P < 0.00001) blocks.

AUTHORS' CONCLUSIONS: ICB is as safe and effective as any other BPBs, regardless of whether ultrasound or neurostimulation guidance is used. The advantages of ICB include a lower likelihood of tourniquet pain during surgery, more reliable blockade of the musculocutaneous nerve when compared to a single-injection axillary block, and a significantly shorter block performance time compared to multi-injection axillary and mid-humeral blocks.

摘要

背景

目前有多种方法可实现臂丛神经的局部麻醉阻滞。虽然锁骨下阻滞(ICB)据称有诸多优势,但对于为下臂手术提供麻醉而言,哪种技术是首选并不明确。因此,我们对锁骨下阻滞与其他臂丛神经阻滞(BPB)进行了系统评价。本评价最初发表于2010年,并于2013年更新。

目的

本评价的目的是评估锁骨下阻滞(ICB)与臂丛神经其他阻滞方法相比,在为下臂手术提供区域麻醉方面的有效性和安全性。

检索方法

我们检索了Cochrane图书馆(2013年第5期)中的Cochrane对照试验中心注册库(CENTRAL);通过OvidSP检索MEDLINE(1966年至2013年6月);通过OvidSP检索EMBASE(1980年至2013年6月)。我们还检索了会议论文集(2004年至2012年)以及www.clinicaltrials.gov试验注册库。最初的评价检索于2008年9月进行。

入选标准

我们纳入了任何将锁骨下阻滞与其他臂丛神经阻滞作为下臂手术唯一麻醉技术进行比较的随机对照试验(RCT)。

数据收集与分析

主要结局是阻滞完成后30分钟内手术麻醉充分。次要结局包括各神经的感觉阻滞、止血带疼痛、感觉阻滞的起效时间、阻滞操作时间、阻滞相关疼痛以及与阻滞相关的并发症。

主要结果

在我们最初的评价中,我们纳入了15项研究,共1020名参与者,排除了2项研究。在本次更新的评价中,我们纳入了7项新研究,排除了6项,纳入研究总数达到22项,涉及1732名参与者。对照组干预措施在14项研究中为腋路阻滞,6项研究中为锁骨上阻滞,2项研究中为肱骨中段阻滞,1项研究中为斜角肌间阻滞。1项研究将锁骨下阻滞与腋路和锁骨上阻滞进行了比较。9项研究采用了超声引导下的锁骨下阻滞。阻滞完成后30分钟手术麻醉失败的风险在锁骨下阻滞与所有其他臂丛神经阻滞中相似(11.4%对12.9%,风险比(RR)0.88,95%置信区间0.51至1.52,P = 0.64),但锁骨下阻滞时止血带疼痛的可能性较小(11.9%对18.0%;经历止血带疼痛的RR为0.66,95%置信区间0.47至0.92,P = 0.02)。按神经定位方法和对照组干预措施进行的亚组分析未显示手术麻醉失败风险有任何统计学上的显著差异。然而,与单次注射腋路阻滞相比,锁骨下阻滞在提供肌皮神经完全感觉阻滞方面更好(失败的RR为0.46,95%置信区间0.27至0.60,P < 0.0001)。锁骨下阻滞的感觉阻滞起效时间略长(平均差(MD)1.9分钟,95%置信区间0.2至3.6,P = 0.03),但操作比多次注射腋路阻滞(MD -2.7分钟,95%置信区间 -3.4至 -2.0,P < 0.00001)或肱骨中段阻滞(MD -4.8分钟,95%置信区间 -6.0至 -3.6,P < 0.00001)更快。

作者结论

无论使用超声还是神经刺激引导,锁骨下阻滞与其他任何臂丛神经阻滞一样安全有效。锁骨下阻滞的优势包括手术期间止血带疼痛的可能性较低,与单次注射腋路阻滞相比,对肌皮神经的阻滞更可靠,以及与多次注射腋路和肱骨中段阻滞相比,阻滞操作时间显著更短。

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