Efficacy and Harms of Pharmacological Interventions for Anxiety after Traumatic Brain Injury: Systematic Review

被引:2
|
作者
Hicks, Amelia J. [1 ]
Clay, Fiona J. [2 ,3 ,4 ]
Hopwood, Malcolm [2 ,3 ,4 ]
James, Amelia C. [1 ]
Perry, Luke A. [2 ]
Jayaram, Mahesh [2 ]
Batty, Rachel [2 ]
Ponsford, Jennie L. [1 ]
机构
[1] Monash Univ, Monash Epworth Rehabil Res Ctr, Turner Inst Brain & Mental Hlth, Sch Psychol Sci, Melbourne, Vic, Australia
[2] Univ Melbourne, Albert Rd Clin, Dept Psychiat, Melbourne, Vic, Australia
[3] Univ Melbourne, Albert Rd Clin, Professorial Psychiat Unit, Melbourne, Vic, Australia
[4] Monash Univ, Dept Forens Med, Southbank, Vic, Australia
关键词
anxiety; pharmacotherapy; review; traumatic brain injury; POSTTRAUMATIC-STRESS-DISORDER; OBSESSIVE-COMPULSIVE DISORDER; LONG-TERM TREATMENT; QUALITY-OF-LIFE; PSYCHIATRIC-DISORDERS; AXIS-I; BEHAVIOR DISORDERS; MAJOR DEPRESSION; SEXUAL CHANGES; RISK-FACTORS;
D O I
10.1089/neu.2020.7277
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
After a traumatic brain injury (TBI), many persons experience significant and debilitating problems with anxiety. The aim of this systematic review was to critically evaluate the evidence regarding efficacy of pharmacological interventions for anxiety after TBI. We reviewed studies published in English before July 2020 and included original research on pharmacological interventions for anxiety after TBI in adults >= 16 years of age. 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 symptoms of anxiety and occurrence of harms. The secondary outcomes of interest were changes in depression, cognition, quality of life, and participation. Data were summarized in a narrative synthesis, and evidence quality was assessed using the Cochrane Risk of Bias tool. Only a single non-peer-reviewed, randomized controlled trial of 19 male military service members with mild TBI met inclusion criteria. This study found no significant effect of citalopram on anxiety symptoms over a 12-week intervention. The trial was stopped early because of poor recruitment, and much of the study detail was not included in the report. The methodological quality of the study was difficult to assess because of the lack of detail. No recommendations could be drawn from this review. There is a critical need for adequately powered and controlled studies of pharmacological interventions for anxiety after TBI across all severities that examine side-effect profiles and consider issues of comorbidity and effects of long-term pharmacotherapy.
引用
收藏
页码:519 / 528
页数:10
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