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鞘内注射吗啡用于脊柱手术后疼痛控制的疗效和安全性:系统评价和荟萃分析。

Efficacy and safety of intrathecal morphine for pain control after spinal surgery: a systematic review and meta-analysis.

机构信息

Department of Pain, Zaozhuang Municipal Hospital, Zaozhuang, Shandong Province, P.R. China.

出版信息

Eur Rev Med Pharmacol Sci. 2021 Mar;25(6):2674-2684. doi: 10.26355/eurrev_202103_25431.

Abstract

This study aimed to assess the efficacy and safety of intrathecal (IT) morphine for postoperative pain control in adults undergoing spinal surgeries. We searched the electronic databases of PubMed, Embase, and CENTRAL up to 1st January 2021 for randomized controlled trials (RCTs) or controlled clinical trials (CCTs) comparing IT morphine with placebo or other analgesics. Twelve studies were included. Eleven were RCTs and one was a CCT. Our meta-analysis indicated a statistically significant reduction of pain scores with IT morphine at 2 hours, 4 hours, 6 hours, 8 hours, 12 hours, and 24 hours; but no significant difference at 48 hours. Meta-analysis indicated a statistically significant reduction in analgesic consumption with IT morphine as compared to control. Pooled analysis indicated that IT morphine had no statistically significant effect on length of hospital stay. Our analysis indicated no statistically significant difference in the risk of nausea, vomiting, sedation, respiratory depression, headache, and urinary retention between IT morphine and control groups. The incidence of pruritis was significantly increased in the IT morphine group. The certainty of the evidence was judged to be "moderate" for pain scores at 12 hours, 24 hours, and analgesic consumption. To conclude, our review indicates that IT morphine results in significantly better pain control in the first 24 hours after spinal surgery. The risk of pruritis is significantly increased with the use of IT morphine but not for other opioid-related adverse events. Future RCTs should focus on finding the most optimal dose of IT morphine for spinal surgeries.

摘要

本研究旨在评估鞘内(IT)吗啡在成人脊柱手术后用于术后疼痛控制的疗效和安全性。我们检索了 PubMed、Embase 和 CENTRAL 电子数据库,截至 2021 年 1 月 1 日,以比较 IT 吗啡与安慰剂或其他镇痛药的随机对照试验(RCT)或对照临床试验(CCT)。共纳入 12 项研究。其中 11 项为 RCT,1 项为 CCT。我们的荟萃分析表明,与安慰剂或其他镇痛药相比,IT 吗啡在 2 小时、4 小时、6 小时、8 小时、12 小时和 24 小时时疼痛评分显著降低;但在 48 小时时无显著差异。与对照组相比,IT 吗啡的镇痛药物消耗明显减少。汇总分析表明,IT 吗啡对住院时间无统计学意义的影响。我们的分析表明,在恶心、呕吐、镇静、呼吸抑制、头痛和尿潴留的风险方面,IT 吗啡与对照组之间无统计学意义的差异。与对照组相比,鞘内吗啡组瘙痒的发生率显著增加。我们判断证据的确定性为“中度”,即 12 小时和 24 小时的疼痛评分以及镇痛药物消耗。总之,我们的综述表明,IT 吗啡可显著改善脊柱手术后 24 小时内的疼痛控制。与 IT 吗啡相关的瘙痒风险显著增加,但其他与阿片类药物相关的不良事件风险没有增加。未来的 RCT 应侧重于寻找最适合脊柱手术的 IT 吗啡剂量。

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