Hicks Amelia J, Clay Fiona J, Hopwood Malcolm, James Amelia C, Jayaram Mahesh, Perry Luke A, Batty Rachel, Ponsford Jennie L
Monash-Epworth Rehabilitation Research Centre, Turner Institute for Brain and Mental Health, Monash University, Melbourne, VIC, Australia.
Department of Psychiatry, University of Melbourne, Melbourne, VIC, Australia.
Front Neurol. 2019 Nov 29;10:1169. doi: 10.3389/fneur.2019.01169. eCollection 2019.
Aggression is a commonly reported problem following traumatic brain injury (TBI). It may present as verbal insults or outbursts, physical assaults, and/or property destruction. Aggressive behavior can fracture relationships and impede participation in treatment as well as a broad range of vocational and social activities, thereby reducing the individual's quality of life. Pharmacological intervention is frequently used to control aggression following TBI. The aim of this systematic review was to critically evaluate the evidence regarding efficacy of pharmacological interventions for aggression following TBI in adults. We reviewed studies in English, available before December 2018. MEDLINE, PubMed, CINAHL, EMBASE, PsycINFO, and CENTRAL databases were searched, with additional searching of key journals, clinical trials registries, and international drug regulators. The primary outcomes of interest were reduction in the severity of aggression and occurrence of harms. The secondary outcomes of interest were changes in quality of life, participation, psychological health (e.g., depression, anxiety), and cognitive function. Evidence quality was assessed using the Cochrane Risk of Bias tool and the Joanna Briggs Institute Critical Appraisal Instruments. Ten studies were identified, including five randomized controlled trials (RCTs) and five case series. There were positive, albeit mixed, findings for the RCTs examining the use of amantadine in reducing irritability ( = 2) and aggression ( = 2). There were some positive findings favoring methylphenidate in reducing anger ( = 1). The evidence for propranolol was weak ( = 1). Individual analysis revealed differential drug response across individuals for both methylphenidate and propranolol. The less rigorous studies administered carbamazepine ( = 2), valproic acid ( = 1), quetiapine ( = 1), and sertraline ( = 1), and all reported reductions in aggression. However, given the lack of a control group, it is difficult to discern treatment effects from natural change over time. This review concludes that a recommendation for use of amantadine to treat aggression and irritability in adults following TBI is appropriate. However, there is a need for further well-designed, adequately powered and controlled studies of pharmacological interventions for aggression following TBI.
攻击行为是创伤性脑损伤(TBI)后常见的问题。它可能表现为言语侮辱或爆发、身体攻击和/或财产破坏。攻击性行为会破坏人际关系,阻碍参与治疗以及广泛的职业和社交活动,从而降低个人生活质量。药物干预常用于控制TBI后的攻击行为。本系统评价的目的是严格评估关于成人TBI后攻击行为的药物干预疗效的证据。我们检索了2018年12月之前可用的英文研究。检索了MEDLINE、PubMed、CINAHL、EMBASE、PsycINFO和CENTRAL数据库,并额外检索了关键期刊、临床试验注册库和国际药品监管机构。感兴趣的主要结局是攻击严重程度的降低和伤害的发生。感兴趣的次要结局是生活质量、参与度、心理健康(如抑郁、焦虑)和认知功能的变化。使用Cochrane偏倚风险工具和乔安娜·布里格斯研究所批判性评价工具评估证据质量。共识别出10项研究,包括5项随机对照试验(RCT)和5个病例系列。在研究金刚烷胺用于降低易怒性(n = 2)和攻击行为(n = 2)的RCT中,有积极但混杂的结果。有一些支持哌甲酯降低愤怒情绪的积极结果(n = 1)。普萘洛尔的证据较弱(n = 1)。个体分析显示,哌甲酯和普萘洛尔在个体间存在不同的药物反应。不太严格的研究使用了卡马西平(n = 2)、丙戊酸(n = 1)、喹硫平(n = 1)和舍曲林(n = 1),所有研究均报告攻击行为有所减少。然而,由于缺乏对照组,很难区分治疗效果与随时间的自然变化。本评价得出结论,推荐使用金刚烷胺治疗成人TBI后的攻击行为和易怒性是合适的。然而,需要进一步开展设计良好、有足够样本量和对照的TBI后攻击行为药物干预研究。