Llorca P M, Lançon C, Auquier P, Bougerol T
Service de Psychiatrie d'Adultes, CHU Sainte-Marguerite, Marseille.
Encephale. 1996 Jul-Aug;22(4):287-92.
we have realized an open study in a population of chronic schizophrenic inpatients treated with clozapine. The purpose of this study was to investigate the clinical response and the effect of extrapyramidal symptoms of this atypical antipsychotic.
our sample is composed of 25 chronic hospitalized schizophrenics (18 males, 7 females; average age = 36.57, SD = 8.41) with an initial important symptomatology (average score on BPRS = 64.92, SD = 7.99). The weekly assessment was done using PANSS and EPRS during 9 weeks. After a 15-days period of treatment adjustment, each patient reached a daily dose of 400 mg. Then the dosage was adjusted according to the clinical condition of the patients (average = 429.41 mg per day).
using the PANSS, we identified a statistically significant (p < 0.05) clinical improvement from the fourth week of treatment for global score, positive, negative and general psychopathology sub-score. For EPRS a dramatic improvement (p < 0.01) occurred from the second week. We found no correlation between the improvement of negative symptoms and the improvement of extrapyramidal symptoms. We individualized a sub-group of 7 good responders who showed an improvement of 20% or more on PANSS global score at the ninth week. This group showed a statistically significant (p < 0.01) more intense initial negative symptomatology compared to non-responders.
the improvement of extrapyramidal symptoms precede the improvement of psychotic symptoms; this effect underlines the good neurological tolerance of clozapine. The clinical efficacy concerns both positive and negative symptoms. The efficacy on negative symptoms seems to be primary. In our sample, patients with intense negative symptomatology improve more than others.
我们对接受氯氮平治疗的慢性精神分裂症住院患者群体进行了一项开放性研究。本研究的目的是调查这种非典型抗精神病药物的临床反应及锥体外系症状的影响。
我们的样本由25名慢性住院精神分裂症患者组成(18名男性,7名女性;平均年龄 = 36.57,标准差 = 8.41),初始症状较为严重(简明精神病评定量表平均得分 = 64.92,标准差 = 7.99)。在9周内使用阳性和阴性症状量表(PANSS)及锥体外系反应量表(EPRS)进行每周评估。经过15天的治疗调整期后,每位患者达到每日400毫克的剂量。然后根据患者的临床状况调整剂量(平均每日 = 429.41毫克)。
使用PANSS,我们发现从治疗第四周起,总体得分、阳性、阴性及一般精神病理学亚得分在临床上有统计学显著改善(p < 0.05)。对于EPRS,从第二周起有显著改善(p < 0.01)。我们发现阴性症状的改善与锥体外系症状的改善之间没有相关性。我们确定了一个由7名良好反应者组成的亚组,他们在第九周时PANSS总体得分改善了20%或更多。与无反应者相比,该组在初始时阴性症状更为严重,具有统计学显著性(p < 0.01)。
锥体外系症状的改善先于精神症状的改善;这一效应突出了氯氮平良好的神经耐受性。临床疗效涉及阳性和阴性症状。对阴性症状的疗效似乎更为主要。在我们的样本中,阴性症状严重的患者比其他患者改善得更多。