Choi-Kwon Smi, Han Sung W, Kwon Sun U, Kang Dong-Wha, Choi Ji M, Kim Jong S
College of Nursing, Seoul National University, Seoul, Korea.
Stroke. 2006 Jan;37(1):156-61. doi: 10.1161/01.STR.0000190892.93663.e2. Epub 2005 Nov 23.
The efficacy and safety of the selective serotonin reuptake inhibitor fluoxetine have rarely been studied in the treatment of poststroke emotional disturbances.
Stroke patients (152) who had poststroke depression (PSD), emotional incontinence (PSEI), or anger proneness (PSAP) were studied. PSD was evaluated by Beck Depression Inventory and Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, PSEI by Kim's criteria, and PSAP was assessed by Spielberger Trait Anger Scale. Subjects were randomly given either fluoxetine 20 mg/day (n=76) or placebo (n=76) for 3 months. Follow-up evaluations were done 1, 3, and 6 months after the beginning of the treatment. The primary outcome measurement was the scores of emotional disturbances at each follow-up assessment. The secondary outcome measurements were the percentage changes of the scores and the subjective responses of the patients.
Although patients in the fluoxetine group more often dropped out because of adverse effects, fluoxetine administration was generally safe. Fluoxetine significantly improved PSEI and PSAP, whereas no definitive improvement of PSD was found. Improvement of PSAP was noted even at 3 months after the discontinuation of the treatment.
Fluoxetine is efficacious in the treatment of PSEI and PSAP. Its effect on PSD is not solidly confirmed.
选择性5-羟色胺再摄取抑制剂氟西汀治疗卒中后情绪障碍的疗效和安全性鲜有研究。
对152例患有卒中后抑郁(PSD)、情绪失禁(PSEI)或易怒倾向(PSAP)的卒中患者进行研究。PSD采用贝克抑郁量表及《精神疾病诊断与统计手册》第四版进行评估,PSEI采用金氏标准评估,PSAP采用斯皮尔伯格特质愤怒量表评估。受试者被随机给予氟西汀20mg/天(n = 76)或安慰剂(n = 76),为期3个月。在治疗开始后的1、3和6个月进行随访评估。主要结局指标是每次随访评估时的情绪障碍评分。次要结局指标是评分的百分比变化及患者的主观反应。
尽管氟西汀组患者因不良反应而退出研究的情况更为常见,但氟西汀的使用总体上是安全的。氟西汀显著改善了PSEI和PSAP,而未发现PSD有明确改善。即使在停药3个月后仍观察到PSAP有所改善。
氟西汀对PSEI和PSAP的治疗有效。其对PSD的疗效尚未得到确凿证实。