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以色列退伍军人的创伤后应激障碍。苯乙肼治疗的效果。

Posttraumatic stress disorder in Israeli combat veterans. Effect of phenelzine treatment.

作者信息

Lerer B, Bleich A, Kotler M, Garb R, Hertzberg M, Levin B

机构信息

Department of Mental Health, Israel Defense Force, Tel Hashomer.

出版信息

Arch Gen Psychiatry. 1987 Nov;44(11):976-81. doi: 10.1001/archpsyc.1987.01800230056010.

DOI:10.1001/archpsyc.1987.01800230056010
PMID:3314769
Abstract

Twenty-five Israeli combat veterans fulfilling DSM-III criteria for posttraumatic stress disorder (PTSD) participated in an open, prospective trial of phenelzine sulfate administration (median daily dose, 60 mg; range, 30 to 90 mg); three patients withdrew early due to side effects. Treatment was continued for at least four weeks in 22 cases and thereafter for as long as it was felt to be of benefit. Therapeutic efficacy was rated using a new PTSD scale, the Hamilton Depression Scale, and the Hamilton Anxiety Scale administered at four weekly intervals. Six patients completed four to eight weeks of phenelzine treatment; seven patients, nine to 13 weeks; and nine patients, 14 to 18 weeks. Comparison of mean prediscontinuation scores with pretreatment ratings showed, at best, only small (23% to 38%) differences (on the PTSD and Hamilton Anxiety scales) in the group treated for nine to 13 weeks. Two patients with a concurrent diagnosis of panic disorder and two with a concurrent diagnosis of dysthymic disorder were the most improved symptomatically but fell short of clinically significant remission. Although statistically significant improvement was observed on seven of the 12 items of the PTSD scale, sleep disturbance was the only symptom showing a clinically impressive change. These results only partially support previous positive reports of phenelzine treatment of PTSD.

摘要

25名符合《精神疾病诊断与统计手册第三版》(DSM - III)创伤后应激障碍(PTSD)标准的以色列退伍军人参加了一项关于硫酸苯乙肼给药的开放性前瞻性试验(每日中位剂量为60毫克;范围为30至90毫克);3名患者因副作用提前退出。22例患者持续治疗至少四周,此后只要认为有益就继续治疗。使用一种新的PTSD量表、汉密尔顿抑郁量表和汉密尔顿焦虑量表,每隔四周进行一次评定来评估治疗效果。6名患者完成了4至8周的苯乙肼治疗;7名患者,9至13周;9名患者,14至18周。将停药前的平均评分与治疗前的评分进行比较,结果显示,在接受9至13周治疗的组中,(在PTSD和汉密尔顿焦虑量表上)最多只有微小的差异(23%至38%)。两名同时诊断为惊恐障碍的患者和两名同时诊断为心境恶劣障碍的患者在症状上改善最为明显,但未达到临床显著缓解。虽然在PTSD量表的12项中有7项观察到了统计学上的显著改善,但睡眠障碍是唯一显示出临床上令人印象深刻变化的症状。这些结果仅部分支持了先前关于苯乙肼治疗PTSD的阳性报告。

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