Which is the best analgesia treatment for total knee arthroplasty: Adductor canal block, periarticular infiltration, or liposomal bupivacaine? A network meta-analysis

内收肌管 医学 止痛药 麻醉 布比卡因 随机对照试验 可视模拟标度 直腿抬高 外科 运动范围 物理疗法 关节置换术
作者
Junheng Chen,Chunbin Zhou,Chuzhou Ma,Guoliang Sun,Lianxiong Yuan,Ziqing Hei,Chunming Guo,Weifeng Yao
出处
期刊:Journal of Clinical Anesthesia [Elsevier BV]
卷期号:68: 110098-110098 被引量:23
标识
DOI:10.1016/j.jclinane.2020.110098
摘要

To review all randomized controlled trials (RCTs) comparing the analgesic efficacy of adductor canal block (ACB), periarticular infiltration (PAI), and any other mode of these treatments in analgesia, such as PAI with liposomal bupivacaine (LB), continuous adductor canal block (cACB) or ACB + PAI, after total knee arthroplasty (TKA). Systematic review and network meta-analysis of RCTs. We searched PubMed, Embase, and the Cochrane database to detect all relevant RCTs on investigating the analgesic effects of ACB, PAI and LB for TKA published until April 2020. Use of different analgesic methods of ACB, PAI, cACB, ACB + PAI and LB. The primary endpoint was visual analog scale (VAS) score at rest and movement. The secondary endpoints were opioids consumption, length of hospitalization and knee range of motion (ROM). We used Cochrane risk of bias to assess the quality of evidence for outcomes. Forty-two studies involving 3785 patients with 5 different methods containing ACB, PAI, ACB + PAI, continuous ACB (cACB), LB, were evaluated. According to surface under the cumulative ranking curve value, 24 h resting VAS score was the lowest the ACB + PAI (88.4%), followed by cACB (73.4%); Resting VAS score at 48 h and movement VAS score at 24 h and 48 h was the lowest in the cACB (99.9%, 92% and 100%). Total opioids consumption was the least in LB (81.4%) before cACB (60.8%). ROM was the largest in the ACB + PAI (84.1%) before cACB (78.8%). Although all analgesic methods available were not evaluated, and further studies are needed to establish our results, the 24 h resting VAS score was lowest in ACB + PAI and 48 h resting and movement VAS score was lowest in cACB. Clinical trial registration: PROSPERO (CRD 42020168102).
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