Department of Anaesthesia, Toronto Western Hospital, University of Toronto, Toronto, Canada.
Anaesthesia. 2013 Feb;68(2):190-202. doi: 10.1111/j.1365-2044.2012.07337.x. Epub 2012 Nov 1.
Eighteen published trials have examined the use of neuraxial magnesium as a peri-operative adjunctive analgesic since 2002, with encouraging results. However, concurrent animal studies have reported clinical and histological evidence of neurological complications with similar weight-adjusted doses. The objectives of this quantitative systematic review were to assess both the analgesic efficacy and the safety of neuraxial magnesium. Eighteen trials comparing magnesium with placebo were identified. The time to first analgesic request increased by 11.1% after intrathecal magnesium administration (mean difference: 39.6 min; 95% CI 16.3-63.0 min; p = 0.0009), and by 72.2% after epidural administration (mean difference: 109.5 min; 95% CI 19.6-199.3 min; p = 0.02) with doses of between 50 and 100 mg. Four trials monitored for neurological complications: of the 140 patients included, only a 4-day persistent headache was recorded. Despite promising peri-operative analgesic effect, the risk of neurological complications resulting from neuraxial magnesium has not yet been adequately defined.
自 2002 年以来,已有 18 项已发表的试验研究了鞘内镁作为围手术期辅助镇痛剂的使用,结果令人鼓舞。然而,同时进行的动物研究报告了类似的体重调整剂量下具有临床和组织学证据的神经并发症。本定量系统评价的目的是评估鞘内镁的镇痛效果和安全性。共确定了 18 项比较镁与安慰剂的试验。鞘内给予镁后首次镇痛请求的时间增加了 11.1%(平均差异:39.6 分钟;95%CI 16.3-63.0 分钟;p=0.0009),硬膜外给予镁后增加了 72.2%(平均差异:109.5 分钟;95%CI 19.6-199.3 分钟;p=0.02),剂量在 50 至 100mg 之间。四项试验监测了神经并发症:在纳入的 140 名患者中,仅记录到持续 4 天的头痛。尽管围手术期镇痛效果有一定的前景,但鞘内镁引起的神经并发症的风险尚未得到充分定义。