抗精神病药物对创伤性脑损伤患者认知和运动功能的影响:临床前研究的系统回顾》。

IF 1.8 Q3 CLINICAL NEUROLOGY
Neurotrauma reports Pub Date : 2024-03-05 eCollection Date: 2024-01-01 DOI:10.1089/neur.2023.0108
Gabrielle Cataford, Laurie-Anne Monton, Stephanie Karzon, Camille Livernoche-Leduc, Mar Saavedra-Mitjans, Marie-Julie Potvin, Francis Bernard, Lisa Burry, Caroline Arbour, David R Williamson
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引用次数: 0

摘要

创伤性脑损伤(TBI)幸存者经常会出现激动行为,并很可能会接受药物治疗。选择一种不会干扰神经系统恢复的最佳安全治疗方法仍存在争议。通过干扰多巴胺能回路,抗精神病药物可能会阻碍对认知恢复非常重要的过程。尽管抗精神病药物经常被使用,但目前还没有关于抗精神病药物治疗急性创伤性脑损伤恢复期躁动行为的大型随机对照研究。我们对评估创伤后抗精神病药物对认知和运动恢复影响的临床前研究进行了系统回顾和荟萃分析。对MEDLINE和Embase数据库的检索截止到2023年8月2日。研究考虑了评估抗精神病药物对创伤后认知和运动功能影响的临床前研究。使用实验室动物实验系统回顾中心(SYRCLE)工具对偏倚风险进行了评估。我们确定了 15 项研究,共涉及 1188 只啮齿类动物,这些研究大多以雄性 Sprague-Dawley 大鼠为对象,使用了皮层撞击损伤的方法。分析结果显示,氟哌啶醇对运动功能没有一致的影响,但利培酮与损伤后第 5 天运动功能的显著损害有关(7.05 秒;95% 置信区间 [CI]:1.47,12.62;I2 = 92%)。其他非典型抗精神病药物不会导致运动功能受损。在评估认知功能时,与对照组相比,氟哌啶醇(23.00 秒;95% 置信区间:17.42-28.59;I2 = 7%)和利培酮(24.27 秒;95% 置信区间:16.18-32.36;I2 = 0%)治疗的大鼠的认知功能持续受损。在评估非典型抗精神病药物的研究中,未观察到任何损害。临床医生应避免经常使用氟哌啶醇和利培酮,今后应使用非典型抗精神病药物进行人体研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cognitive and Motor Function Effects of Antipsychotics in Traumatic Brain Injury: A Systematic Review of Pre-Clinical Studies.

Traumatic brain injury (TBI) survivors often suffer from agitated behaviors and will most likely receive pharmacological treatments. Choosing an optimal and safe treatment that will not interfere with neurological recovery remains controversial. By interfering with dopaminergic circuits, antipsychotics may impede processes important to cognitive recovery. Despite their frequent use, there have been no large randomized controlled studies of antipsychotics for the management of agitated behaviors during the acute TBI recovery period. We conducted a systematic review and meta-analysis of pre-clinical studies evaluating the effects of antipsychotics post-TBI on both cognitive and motor recovery. MEDLINE and Embase databases were searched up to August 2, 2023. Pre-clinical studies evaluating the effects of antipsychotics on cognitive and motor functions post-TBI were considered. Risk of bias was evaluated with the Systematic Review Centre for Laboratory Animal Experimentation (SYRCLE) tool. We identified 15 studies including a total of 1188 rodents, mostly conducted in male Sprague-Dawley rats using cortical impact injury. The analysis revealed no consistent effect of haloperidol on motor functions, but risperidone was associated with a significant impairment in motor function on day 5 post-injury (7.05 sec; 95% confidence interval [CI]: 1.47, 12.62; I2 = 92%). Other atypical antipsychotics did not result in impaired motor function. When evaluating cognitive function, haloperidol- (23.00 sec; 95% CI: 17.42-28.59; I2 = 7%) and risperidone-treated rats (24.27 sec; 95% CI: 16.18-32.36; I2 = 0%) were consistently impaired when compared to controls. In studies evaluating atypical antipsychotics, no impairments were observed. Clinicians should avoid the regular use of haloperidol and risperidone, and future human studies should be conducted with atypical antipsychotics.

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