Juul Povlsen U, Noring U, Fog R, Gerlach J
Acta Psychiatr Scand. 1985 Feb;71(2):176-85. doi: 10.1111/j.1600-0447.1985.tb01268.x.
Two hundred and sixteen psychiatric patients (183 men and 33 women) hospitalized in Sct. Hans Hospital were treated with clozapine between 1971-1983. All had been treated previously with one or more neuroleptic(s) and had either failed to respond adequately, or their response was limited by side effects. Eighty-five patients were treated exclusively with clozapine, while the remaining 131 received additional medication, mainly other neuroleptic drugs. The mean clozapine dosage was 317 mg/day (range 50-1200), and the mean duration of treatment was 23/4 years (range 1/12-12). The tolerability to clozapine was determined by an evaluation of haematological changes, pronounced side effects and mortality. One patient treated with clozapine (8 months) and nitrofurantoin (8 days) developed a reversible granulocytopenia. One patient (treated with a combination of drugs) had clinically insignificant depression of the leucocytes and three of segmented granulocytes. Seven had a reduction in thrombocytes. Two patients developed cardiac insufficiency, and four epileptic seizures. None of the patients treated exclusively with clozapine developed neurological side effects. A global estimation of therapeutic effect revealed that clozapine alone or in combination with other neuroleptic drugs was significantly better than previous antipsychotic therapy, although 47-63% of the patients showed no change. It is concluded that clozapine is a potent antipsychotic drug offering particular advantages in the treatment of schizophrenic patients with a pronounced symptomatology and tendency towards developing extrapyramidal side effects. Caution is advised in patients with cardiac insufficiency and epilepsy. There appears to be a slight risk of granulocytopenia, and therefore the present monitoring of WBC should continue in order to prevent this reaction and to obtain more complete information regarding risk of granulocytopenia.
1971年至1983年间,在斯堪的纳维亚的汉斯医院住院的216名精神科患者(183名男性和33名女性)接受了氯氮平治疗。所有患者此前均接受过一种或多种抗精神病药物治疗,要么疗效不佳,要么因副作用而疗效受限。85名患者仅接受氯氮平治疗,其余131名患者还接受了其他药物治疗,主要是其他抗精神病药物。氯氮平的平均剂量为317毫克/天(范围为50 - 1200毫克),平均治疗持续时间为2又3/4年(范围为1/12 - 12年)。通过评估血液学变化、明显的副作用和死亡率来确定对氯氮平的耐受性。一名接受氯氮平治疗8个月和呋喃妥因治疗8天的患者出现了可逆性粒细胞减少。一名患者(接受联合药物治疗)白细胞和中性粒细胞轻度减少,7名患者血小板减少。2名患者出现心脏功能不全,4名患者发生癫痫发作。仅接受氯氮平治疗的患者均未出现神经方面的副作用。对治疗效果的总体评估显示,单独使用氯氮平或与其他抗精神病药物联合使用明显优于先前的抗精神病治疗,尽管47% - 63%的患者病情无变化。结论是,氯氮平是一种强效抗精神病药物,在治疗有明显症状且有发生锥体外系副作用倾向的精神分裂症患者方面具有特殊优势。对心脏功能不全和癫痫患者建议谨慎使用。似乎存在轻微的粒细胞减少风险,因此应继续目前对白细胞的监测,以预防这种反应并获取有关粒细胞减少风险的更完整信息。