长效抗精神病药癸酸氟哌辛醇和癸酸氟那嗪在精神分裂症维持治疗中的开放临床试验

Pharmatherapeutica Pub Date : 1989-01-01
D S Kong, S H Yeo
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引用次数: 0

摘要

对21例慢性精神分裂症患者进行了开放性临床试验,以评估贮存抗精神病药治疗的有效性和副作用。所有患者使用癸酸氟那嗪至少稳定6个月,并且在进入研究时给予继续使用该治疗或改用癸酸氟苯辛醇的选择。16例患者选择接受癸酸氟苯乙醇(40 mg),另外5例氟非那嗪(25 mg)。在12周的研究期间,每4周给药一次。临床评估每4周进行一次(第0、4、8和12周),使用简短精神病学评定量表和副作用清单,以及汉密尔顿抑郁症评定量表、受影响障碍和精神分裂症时间表-修改版和总体评估量表,在进入(第0周)和研究结束(第12周)时完成。结果表明,氟苯乙醇组患者抑郁、戒断、焦虑、精神运动迟缓症状的改善明显优于氟非那嗪组(p < 0.05)。氟哌啶醇治疗期间副作用发生率降低,治疗8周后,氟哌啶醇组副作用发生率低于氟非那嗪组。结论是,一组以抑郁症状或处方抗精神病药副作用为特征的精神分裂症患者可能从切换到氟苯硫醇治疗中受益。
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An open clinical trial with the long-acting neuroleptics flupenthixol decanoate and fluphenazine decanoate in the maintenance treatment of schizophrenia.

An open clinical trial was carried out in 21 chronic schizophrenics to assess the effectiveness and side-effects of treatment with depot neuroleptics. All patients had been stabilized on fluphenazine decanoate for at least 6 months and on entry to the study were given the choice of continuing with this treatment or changing over to flupenthixol decanoate. Sixteen patients chose to receive flupenthixol decanoate (40 mg) and the other 5 fluphenazine decanoate (25 mg). Doses were given every 4 weeks during the 12-week study period. Clinical assessments were carried out every 4 weeks (Weeks 0, 4, 8 and 12) using the Brief Psychiatric Rating Scale and a side-effects checklist, and the Hamilton Rating Scale for Depression, the Schedule for Affected Disorders and Schizophrenia--Change Version, and the Global Assessment Scale were completed on entry (Week 0) and at the end of the study (Week 12). The results indicated that symptoms of depression, withdrawal, worrying, and psychomotor retardation were improved significantly (p less than 0.05) more with flupenthixol than with fluphenazine. The frequency of side-effects decreased during treatment with flupenthixol and there was a tendency towards fewer side-effects in the flupenthixol group than in the fluphenazine group after 8 weeks of treatment. It is concluded that a group of schizophrenic patients characterized by depressive symptoms or side-effects attributable to a prescribed neuroleptic might benefit from a switch to flupenthixol treatment.

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