Reding M J, Orto L A, Winter S W, Fortuna I M, Di Ponte P, McDowell F H
Arch Neurol. 1986 Aug;43(8):763-5. doi: 10.1001/archneur.1986.00520080011011.
Twenty-seven inpatients participating in a stroke rehabilitation program were randomized to receive either placebo or trazodone hydrochloride (Desyrel) beginning a mean (+/- SEM) of 44 +/- 4 days after stroke. The target dosage was 200 mg/d. Patients with either a clinical diagnosis of depression or abnormal Zung depression scores showed a consistent trend toward greater improvement in Barthel activities of daily living (ADL) scores with trazodone than with placebo. An abnormal dexamethasone suppression test result was associated with significant improvement in the Barthel ADL scores of patients receiving trazodone (38 +/- 6 vs 20 +/- 6 for placebo). Patients with stroke and evidence of depression are therefore likely to benefit from treatment with trazodone.
27名参加中风康复计划的住院患者被随机分组,自中风后平均(±标准误)44±4天起,分别接受安慰剂或盐酸曲唑酮(安适定)治疗。目标剂量为200毫克/天。临床诊断为抑郁症或Zung抑郁评分异常的患者,与接受安慰剂治疗相比,接受曲唑酮治疗的患者在Barthel日常生活活动(ADL)评分上有持续更大幅度改善的趋势。地塞米松抑制试验结果异常与接受曲唑酮治疗患者的Barthel ADL评分显著改善相关(安慰剂组为20±6,曲唑酮组为38±6)。因此,患有中风且有抑郁症证据的患者可能会从曲唑酮治疗中获益。