急性功能性精神病:用盐酸夏绿戊硫醇片治疗。

Pharmatherapeutica Pub Date : 1987-01-01
S N Bhattacharyya, J Ghoshal, S K Sharma, N Halstead, B John, M A Launer, P K Mukherjee, A S Zigmond
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引用次数: 0

摘要

在一项开放的多中心研究中,对63例患者进行了二盐酸zuclopenthixol片治疗急性精神病发作的疗效和耐受性评估。大多数患者在进入研究之前已经接受了其他抗精神病药物,但效果不足。在为期10周的研究中,可调整盐酸zuclopenthixol片的剂量,以获得最佳的临床疗效。在研究开始时,大多数患者每天服用20至75毫克(范围为每天10至150毫克),后来,对于大多数成功治疗的患者,剂量为每天20至55毫克。治疗前和治疗期间的评估采用了BPRS和CGI评分量表以及副作用检查表。50例精神分裂症或精神分裂样精神病患者中有70%对治疗有成功反应,13例躁狂或轻躁狂患者中有69%对治疗有成功反应。几乎一半(30)的研究患者在开始治疗的4周内成功缓解,有些患者仅在治疗1周后就成功缓解。除1名患者外,所有患者要么没有副作用,要么副作用没有明显影响表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acute functional psychoses: treatment with zuclopenthixol dihydrochloride ('Clopixol') tablets.

An assessment of the efficacy and tolerability of zuclopenthixol dihydrochloride tablets in the treatment of acute psychotic episodes was undertaken in 63 patients in an open multi-centre study. Most patients prior to entering the study had received other neuroleptic drugs, but with inadequate effect. During the 10-week study, the dosage of zuclopenthixol dihydrochloride tablets could be adjusted to obtain optimum clinical benefit. The majority of patients received 20 to 75 mg daily (range 10 to 150 mg daily) at the start of the study and later, for most of those patients successfully treated, the dosage was 20 to 55 mg daily. Assessments before and during treatment utilized the BPRS and CGI rating scales and a check-list of side-effects. A successful response to treatment was achieved in 70% of 50 patients with schizophrenia or schizophreniform psychoses and in 69% of 13 patients with mania or hypomania. Almost half (30) of the patients studied had a successful response within 4 weeks of starting treatment and some after only 1 week of treatment. All patients but 1 had either no side-effects or side-effects not overtly affecting performance.

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