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本文引用的文献

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Cannabinoids in traumatic brain injury and related neuropathologies: preclinical and clinical research on endogenous, plant-derived, and synthetic compounds.创伤性脑损伤及相关神经病理学中的大麻素:内源性、植物源和合成化合物的临床前和临床研究。
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2
Current Clinical Trials in Traumatic Brain Injury.创伤性脑损伤的当前临床试验
Brain Sci. 2022 Apr 21;12(5):527. doi: 10.3390/brainsci12050527.
3
Neuroinflammation as a pathophysiological factor in the development and maintenance of functional seizures: A hypothesis.神经炎症作为功能性癫痫发生和维持的病理生理因素:一种假说。
Epilepsy Behav Rep. 2021 Oct 26;16:100496. doi: 10.1016/j.ebr.2021.100496. eCollection 2021.
4
Cannabidiol (CBD) and cognition in epilepsy.大麻二酚(CBD)与癫痫中的认知
Epilepsy Behav. 2021 Sep 23;124:108316. doi: 10.1016/j.yebeh.2021.108316.
5
Admission Glasgow Coma Scale Score as a Predictor of Outcome in Patients Without Traumatic Brain Injury.格拉斯哥昏迷量表入院评分作为非创伤性脑损伤患者预后的预测指标
Am J Crit Care. 2021 Sep 1;30(5):350-355. doi: 10.4037/ajcc2021163.
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Editorial: Evidence-Based Anti-Inflammatory, Anti-Hypoperfusion and Anti-Anxiety/Insomnia Therapies Show Promises for TBI-Induced Post-Traumatic Symptoms and Cognitive Deficits: Advances in Diagnosis and Treatment of TBI-Induced Neurodegeneration and Cognitive Deficits.社论:基于证据的抗炎、抗低灌注和抗焦虑/失眠疗法对创伤性脑损伤所致创伤后症状和认知缺陷显示出前景:创伤性脑损伤所致神经退行性变和认知缺陷的诊断与治疗进展
Front Neurol. 2021 Aug 11;12:695629. doi: 10.3389/fneur.2021.695629. eCollection 2021.
7
Cannabis Use and Car Crashes: A Review.大麻使用与汽车撞车事故:一项综述。
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8
Assessing the Severity of Traumatic Brain Injury-Time for a Change?评估创伤性脑损伤的严重程度——是时候做出改变了吗?
J Clin Med. 2021 Jan 4;10(1):148. doi: 10.3390/jcm10010148.
9
Use of Medical Cannabis to Treat Traumatic Brain Injury.医用大麻治疗创伤性脑损伤。
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10
Understanding neurodegeneration after traumatic brain injury: from mechanisms to clinical trials in dementia.创伤性脑损伤后神经退行性变的理解:从机制到痴呆症的临床试验。
J Neurol Neurosurg Psychiatry. 2019 Nov;90(11):1221-1233. doi: 10.1136/jnnp-2017-317557. Epub 2019 Sep 21.

使用消遣性大麻后的创伤性脑损伤结果

Traumatic Brain Injury Outcomes After Recreational Cannabis Use.

作者信息

Szaflarski Jerzy P, Szaflarski Magdalena

机构信息

Department of Neurology, University of Alabama at Birmingham (UAB), Heersink School of Medicine, Birmingham, AL, USA.

Department of Sociology, University of Alabama at Birmingham (UAB), Birmingham, AL, USA.

出版信息

Neuropsychiatr Dis Treat. 2024 Apr 3;20:809-821. doi: 10.2147/NDT.S453616. eCollection 2024.

DOI:10.2147/NDT.S453616
PMID:38586307
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10999198/
Abstract

PURPOSE

Basic science data indicate potential neuroprotective effects of cannabinoids in traumatic brain injury (TBI). We aimed to evaluate the effects of pre-TBI recreational cannabis use on TBI outcomes.

PATIENTS AND METHODS

We used i2b2 (a scalable informatics framework; www.i2b2.org) to identify all patients presenting with acute TBI between 1/1/2014 and 12/31/2016, then conducted a double-abstraction medical chart review to compile basic demographic, urine drug screen (UDS), Glasgow Coma Scale (GCS), and available outcomes data (mortality, modified Rankin Scale (mRS), duration of stay, disposition (home, skilled nursing facility, inpatient rehabilitation, other)) at discharge and at specific time points thereafter. We conducted multivariable nested ordinal and logistic regression analyses to estimate associations between cannabis use, other UDS results, demographic factors, and selected outcomes.

RESULTS

i2b2 identified 6396 patients who acutely presented to our emergency room with TBI. Of those, 3729 received UDS, with 22.2% of them testing positive for cannabis. Mortality was similar in patients who tested positive vs negative for cannabis (3.9% vs 4.8%; p = 0.3) despite more severe GCS on admission in the cannabis positive group (p = 0.045). Several discharge outcome measures favored the cannabis positive group who had a higher rate of discharge home vs other care settings (p < 0.001), lower discharge mRS (p < 0.001), and shorter duration of hospital stay (p < 0.001) than the UDS negative group. Multivariable analyses confirmed mostly independent associations between positive cannabis screen and these post-TBI short- and long-term outcomes.

CONCLUSION

This study adds evidence about the potentially neuroprotective effects of recreational cannabis for short- and long-term post-TBI outcomes. These results need to be confirmed via prospective data collections.

摘要

目的

基础科学数据表明大麻素对创伤性脑损伤(TBI)具有潜在的神经保护作用。我们旨在评估创伤性脑损伤前使用娱乐性大麻对TBI预后的影响。

患者与方法

我们使用i2b2(一个可扩展的信息学框架;www.i2b2.org)来识别2014年1月1日至2016年12月31日期间所有出现急性TBI的患者,然后进行双份病历审查,以汇总基本人口统计学、尿液药物筛查(UDS)、格拉斯哥昏迷量表(GCS)以及出院时和此后特定时间点的可用预后数据(死亡率、改良Rankin量表(mRS)、住院时间、出院处置情况(回家、专业护理机构、住院康复、其他))。我们进行了多变量嵌套有序和逻辑回归分析,以估计大麻使用、其他UDS结果、人口统计学因素与选定预后之间的关联。

结果

i2b2识别出6396例急性到我们急诊室就诊的TBI患者。其中,3729例接受了UDS检测,其中22.2%的患者大麻检测呈阳性。大麻检测呈阳性与阴性的患者死亡率相似(3.9%对4.8%;p = 0.3),尽管大麻阳性组入院时GCS评分更严重(p = )。与UDS阴性组相比,大麻阳性组在几个出院预后指标方面表现更好,回家出院率更高(p < 0.001),出院时mRS更低(p < 0.001),住院时间更短(p < 0.001)。多变量分析证实,大麻筛查阳性与这些TBI后短期和长期预后之间大多存在独立关联。

结论

本研究补充了关于娱乐性大麻对TBI后短期和长期预后可能具有神经保护作用的证据。这些结果需要通过前瞻性数据收集来证实。 (注:原文中“p = 0.045”处括号内缺少具体数字,“p = ”处也缺少具体数字,翻译时保留原文格式)