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Scalp block for analgesia after craniotomy: A meta-analysis

机译:开颅手术后镇痛的头皮阻滞:一项荟萃分析

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Background and Aims: A previous meta-analysis reported that scalp block had limited benefits (low-quality evidence) compared to no-scalp block modalities for analgesia after craniotomy. However, it included studies using two different pain intensity measurement scales. Therefore, we performed another meta-analysis using a single scale. Methods: We conducted the search for all randomised controlled trials evaluating the effect of scalp block on postcraniotomy pain compared to no-scalp block in Cochrane Central Register of Controlled Trials and PubMed database. We assessed the quality of included studies employing GRADE approach. We performed random-effects inverse-variance weighted meta-analysis of outcomes including pain intensity assessed by a 0--10 visual analog scale and opioid consumption during the first 24 h postoperative period using RevMan 5.3. Results: A total of 10 studies (551 patients) were included. It revealed a statistically significant mean pain intensity reduction in scalp block group when compared to no-scalp block at very early and early 24 h period (seven trials, very low-quality evidence, mean difference (MD) = ?1.37, 95% confidence interval (CI): ?2.23 to -0.05, Isup2/sup = 70%; nine trials, very low-quality evidence, MD = ?1.16, 95% CI: ?2.09 to ?0.24, Isup2/sup = 57%, respectively). There was also reduction in the opioid requirements over the first 24 h postoperatively. Conclusion: Scalp block might be useful at 6 h postcraniotomy with very-low quality evidence. Additionally, it had uncertain but moderate effect on reducing total 24 h opioid consumption. Therefore, more studies are needed to reach optimal information size.
机译:背景与目的:先前的一项荟萃​​分析报告说,与开颅手术后的无头皮镇痛方法相比,头皮阻滞的益处有限(证据质量低)。但是,它包括使用两种不同的疼痛强度测量量表进行的研究。因此,我们使用单一标度执行了另一项荟萃分析。方法:我们在Cochrane对照试验中心注册数据库和PubMed数据库中搜索了所有评估头皮阻滞对开颅术后疼痛与无头皮阻滞效果的随机对照试验。我们使用GRADE方法评估了纳入研究的质量。我们使用RevMan 5.3对术后结果进行了随机效果反方差加权荟萃分析,包括0--10视觉模拟量表评估的疼痛强度和阿片类药物的摄入量(5.3版)。结果:共纳入10项研究(551例患者)。结果显示,在24小时的早期和早期,与无头皮阻滞相比,头皮阻滞组的平均疼痛强度降低具有统计学意义(七项试验,非常低质量的证据,平均差异(MD)= 1.37,置信度为95%区间(CI):? 2.23至-0.05,I 2 = 70%;九项试验,非常低质量的证据,MD =?1.16,95%CI:?2.09至?0.24,I < sup> 2 = 57%)。术后头24小时阿片类药物的需求量也减少了。结论:头颅阻滞可能在颅骨切开术后<6 h有用,但证据质量很低。此外,它对减少24小时阿片类药物的总摄入量尚不确定但有中等作用。因此,需要更多的研究来达到最佳信息量。

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