Use of amantadine in traumatic brain injury: an updated meta-analysis of randomized controlled trials.

IF 2.8 3区 医学 Q2 CLINICAL NEUROLOGY Frontiers in Neurology Pub Date : 2025-01-21 eCollection Date: 2024-01-01 DOI:10.3389/fneur.2024.1444623
João Félix, Luísa Araújo, Antônio Henriques, Ana Pereira, Saul Carneiro
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Abstract

Introduction: Amantadine has been shown to accelerate cognitive and functional brain recovery after cerebrovascular accidents. However, the efficacy of this drug in TBI patients remains poorly defined.

Methods: We performed a systematic review and meta-analysis of randomized trials (RCTs) evaluating the effects of amantadine in TBI patients. The Cochrane, Embase, and PubMed databases were systematically searched for trials published up to March 24, 2024. Data from previous RCTs were extracted and quality assessed according to Cochrane recommendations. Means and standard deviations with 95% confidence intervals were aggregated across studies. The primary outcomes assessed were Glasgow Coma Scale (GCS), Mini Mental State Examination (MMSE) and the Disability Rating Scale (DRS).

Results: From 1,292 database results, 6 studies with 426 patients were included, of which 205 received amantadine (48.12%). The Glasgow Coma Scale score on day 7 (MD 1.50; 95% CI 0.08-2.92; p = 0.038; I 2 = 68%) was significantly higher in patients treated with amantadine than those treated with placebo. The Mini Mental State Examination (MD 3.23; 95% CI 0.53-5.94; p = 0.019; I 2 = 0%) was also better in patients treated with amantadine. No significant differences in Disability Rating Scale, day 3 GCS, Glasgow Outcome Scale (GOS), length of hospital stay, or duration of mechanical ventilation were observed between amantadine and placebo groups.

Conclusion: In our analysis, TBI patients benefit from the use of amantadine in the day 7 GCS score and show better results in the MMSE test, but placebo patients benefit from not using amantadine in the DRS between weeks 3 and 4. No other statistically significant results were found related to the use of this medication.Systematic review registration: https://www.crd.york.ac.uk/prospero/display_ record.php?ID=CRD42024538110, CRD42024538110.

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金刚烷胺在创伤性脑损伤中的应用:一项随机对照试验的最新荟萃分析。
金刚烷胺已被证明能加速脑血管事故后大脑认知和功能的恢复。然而,该药在TBI患者中的疗效仍不明确。方法:我们对随机试验(rct)进行了系统回顾和荟萃分析,评估金刚烷胺对TBI患者的影响。我们系统地检索了Cochrane、Embase和PubMed数据库,检索了截止到2024年3月24日发表的试验。从以前的随机对照试验中提取数据,并根据Cochrane推荐进行质量评估。95%置信区间的均值和标准差在研究中汇总。评估的主要结果是格拉斯哥昏迷量表(GCS)、迷你精神状态检查(MMSE)和残疾评定量表(DRS)。结果:从1292个数据库结果中,纳入6项研究,426例患者,其中205例接受金刚烷胺治疗,占48.12%。第7天格拉斯哥昏迷评分(MD 1.50;95% ci 0.08-2.92;p = 0.038;I 2 = 68%),金刚烷胺治疗组的患者明显高于安慰剂治疗组。简易精神状态检查(MD 3.23;95% ci 0.53-5.94;p = 0.019;i2 = 0%),金刚烷胺治疗组疗效更好。金刚烷胺组和安慰剂组在残疾评定量表、第3天GCS、格拉斯哥结局量表(GOS)、住院时间或机械通气时间方面均无显著差异。结论:在我们的分析中,TBI患者受益于在第7天的GCS评分中使用金刚烷胺,并且在MMSE测试中显示出更好的结果,但安慰剂患者受益于在第3周至第4周的DRS中不使用金刚烷胺。没有其他统计上显著的结果与使用这种药物有关。系统评审注册:https://www.crd.york.ac.uk/prospero/display_ record.php?ID = CRD42024538110 CRD42024538110。
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来源期刊
Frontiers in Neurology
Frontiers in Neurology CLINICAL NEUROLOGYNEUROSCIENCES -NEUROSCIENCES
CiteScore
4.90
自引率
8.80%
发文量
2792
审稿时长
14 weeks
期刊介绍: The section Stroke aims to quickly and accurately publish important experimental, translational and clinical studies, and reviews that contribute to the knowledge of stroke, its causes, manifestations, diagnosis, and management.
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