Safety and Efficacy of Riluzole in Traumatic Spinal Cord Injury: A Systematic Review With Meta-Analyses.

IF 1.8 Q3 CLINICAL NEUROLOGY
Neurotrauma reports Pub Date : 2024-02-19 eCollection Date: 2024-01-01 DOI:10.1089/neur.2023.0114
Luke J Weisbrod, Thomas T Nilles-Melchert, Judith R Bergjord, Daniel L Surdell
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Abstract

Traumatic spinal cord injury (SCI) is a cause of significant morbidity, often resulting in long-term disability. We aimed to compare outcomes after riluzole versus patients who received placebo or standard of care with no specific intervention. MEDLINE, Embase, Scopus, and Cochrane Library database searches yielded 92 records, and five met the study inclusion criteria. Fixed-effect and random-effects models were used to establish odds ratios (ORs) and mean difference (MD) with 95% confidence intervals (CIs) for each outcome. The results of the pooled analysis showed that in patients with acute traumatic SCI, riluzole resulted in increased American Spinal Injury Association (ASIA) motor scores at 3 months (MD 0.26, 95% CI [-0.10,0.61], I2 = 0%; p = 0.157) and 6 months (MD 0.21, 95% CI [-0.17,0.60], I2 = 0%; p = 0.280) and change in ASIA Impairment Scale (AIS) at 3 months (OR 0.59, 95% CI [-0.12,1.30], I2 = 0%, p = 0.101) and 6 months (OR 0.28, 95% CI [-0.50,1.06], I2 = 0%, p = 0.479) in comparison to the control groups, though not to a level of statistical significance. Riluzole resulted in fewer adverse events than the control groups (OR -0.12, 95% CI [-1.59,1.35], I2 = 0%, p = 0.874) and lower mortality (OR -0.20, 95% CI [-1.03,0.63], I2 = 0%, p = 0.640), though also not to a level of statistical significance. These meta-analyses suggest that riluzole for the treatment of traumatic SCI is safe and results in improved neurological outcomes when compared to controls, though not to a level of statistical significance. More robust prospective, randomized studies are necessary to help inform the safety and efficacy of riluzole for traumatic SCI.

利鲁唑治疗创伤性脊髓损伤的安全性和有效性:带 Meta 分析的系统综述。
创伤性脊髓损伤(SCI)是一种严重的发病原因,通常会导致长期残疾。我们旨在比较利鲁唑与接受安慰剂或无特定干预的标准护理的患者的治疗效果。在 MEDLINE、Embase、Scopus 和 Cochrane Library 数据库中搜索到 92 条记录,其中 5 条符合研究纳入标准。采用固定效应和随机效应模型确定了每种结果的几率比(OR)和平均差(MD),以及 95% 的置信区间(CI)。汇总分析结果显示,在急性创伤性 SCI 患者中,利鲁唑可提高 3 个月时的美国脊柱损伤协会 (ASIA) 运动评分(MD 0.26,95% CI [-0.10,0.61],I2 = 0%;P = 0.157)和 6 个月时的运动评分(MD 0.21,95% CI [-0.17,0.60],I2 = 0%)。60],I2 = 0%;p = 0.280)和 ASIA 损伤量表(AIS)在 3 个月(OR 0.59,95% CI [-0.12,1.30],I2 = 0%,p = 0.101)和 6 个月(OR 0.28,95% CI [-0.50,1.06],I2 = 0%,p = 0.479)时的变化与对照组相比,尽管没有统计学意义。与对照组相比,利鲁唑导致的不良事件较少(OR -0.12,95% CI [-1.59,1.35],I2 = 0%,p = 0.874),死亡率较低(OR -0.20,95% CI [-1.03,0.63],I2 = 0%,p = 0.640),但也未达到统计学意义水平。这些荟萃分析表明,利鲁唑治疗创伤性 SCI 是安全的,与对照组相比,利鲁唑可改善神经功能预后,但未达到统计学显著性水平。有必要开展更多可靠的前瞻性随机研究,以帮助了解利鲁唑治疗创伤性 SCI 的安全性和有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.40
自引率
0.00%
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审稿时长
8 weeks
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