Universidade Federal de Santa Catarina, Departamento de Cirurgia, Florianópolis, SC, Brazil.
Universidade Federal de Santa Catarina, Departamento de Cirurgia, Florianópolis, SC, Brazil.
Braz J Anesthesiol. 2023 Jul-Aug;73(4):455-466. doi: 10.1016/j.bjane.2022.08.005. Epub 2022 Sep 8.
This study evaluated the efficacy of epidurally administered magnesium associated with local anesthetics on postoperative pain control.
The study protocol was registered in PROSPERO as CRD42021231910. Literature searches were conducted on Medline, Cochrane, EMBASE, CENTRAL, and Web of Science for randomized controlled trials comparing epidural administration of magnesium added to local anesthetics for postoperative pain in elective surgical adult patients. Primary outcomes were the time to the first Postoperative (PO) Analgesic Request (TFAR), 24-hour postoperative opioid consumption, and Visual Analog Scale (VAS) scores at the first six and 24 postoperative hours. Secondary outcomes included Postoperative Nausea and Vomiting (PONV), pruritus, and shivering. Quality of evidence was assessed using GRADE criteria.
Seventeen studies comparing epidural were included. Effect estimates are described as weighted Mean Differences (MD) and 95% Confidence Intervals (95% CI) for the main outcomes: TFAR (MD = 72.4 min; 95% CI = 10.22-134.58 min; p < 0.001; I = 99.8%; GRADE: very low); opioid consumption (MD = -7.2 mg (95% CI = -9.30 - -5.09; p < 0.001; I = 98%; GRADE: very low). VAS pain scores within the first six PO hours (VAS) (MD = -1.01 cm; 95% CI = -1.40-0.64 cm; p < 0.001; I = 88%; GRADE: very low), at 24 hours (MD = -0.56 cm; 95% CI = -1.14-0.01 cm; p = 0.05; I = 97%; GRADE: very low).
Magnesium sulfate delayed TFAR and decreased 24-hour opioid consumption and early postoperative pain intensity. However, imprecision and inconsistency pervaded meta-analyses, causing very low certainty of effect estimates.
本研究评估了硬膜外给予镁联合局麻药在术后疼痛控制中的疗效。
该研究方案在 PROSPERO 中注册为 CRD42021231910。对 Medline、Cochrane、EMBASE、CENTRAL 和 Web of Science 进行文献检索,以纳入比较择期手术成年患者硬膜外给予镁联合局麻药用于术后疼痛的随机对照试验。主要结局为首次术后(PO)镇痛请求(TFAR)时间、24 小时术后阿片类药物消耗量以及术后 6 小时和 24 小时的视觉模拟评分(VAS)。次要结局包括术后恶心和呕吐(PONV)、瘙痒和寒战。使用 GRADE 标准评估证据质量。
纳入了 17 项比较硬膜外的研究。主要结局的效应估计值描述为加权均数差(MD)和 95%置信区间(95%CI):TFAR(MD=72.4 分钟;95%CI=10.22-134.58 分钟;p<0.001;I=99.8%;GRADE:极低);阿片类药物消耗量(MD=-7.2mg(95%CI=-9.30-5.09;p<0.001;I=98%;GRADE:极低)。术后 6 小时内的 VAS 疼痛评分(MD=-1.01cm;95%CI=-1.40-0.64cm;p<0.001;I=88%;GRADE:极低)和 24 小时时的 VAS 疼痛评分(MD=-0.56cm;95%CI=-1.14-0.01cm;p=0.05;I=97%;GRADE:极低)。
硫酸镁延迟了 TFAR,并减少了 24 小时阿片类药物的消耗和早期术后疼痛强度。然而,荟萃分析中存在不精确性和不一致性,导致效应估计的确定性非常低。