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难治性精神分裂症患者在三个血清水平范围内对氯氮平的反应。

Response of patients with treatment-refractory schizophrenia to clozapine within three serum level ranges.

作者信息

VanderZwaag C, McGee M, McEvoy J P, Freudenreich O, Wilson W H, Cooper T B

机构信息

John Umstead Hospital, Adult Admission Unit, Butner, NC 27509, USA.

出版信息

Am J Psychiatry. 1996 Dec;153(12):1579-84. doi: 10.1176/ajp.153.12.1579.

DOI:10.1176/ajp.153.12.1579
PMID:8942454
Abstract

OBJECTIVE

This study sought to determine the relationships between serum clozapine levels and therapeutic response.

METHOD

Fifty-six inpatients who met the DSM-III-R criteria for chronic schizophrenia and who had not responded to extended treatment with classical antipsychotics were randomly assigned to 12 weeks of double-blind treatment with clozapine at one of three serum level ranges: low (50-150 ng/ml), medium (200-300 ng/ml), or high (350-450 ng/ml). Baseline clinical assessments were completed before the patients' regular antipsychotic and anticholinergic drugs were discontinued. During clozapine treatment, serum levels were ascertained weekly to allow adjustment of clozapine doses so as to maintain each patient near the midpoint of his or her assigned serum level range. Clinical assessments were completed after 6 and 12 weeks of treatment.

RESULTS

The analyses of the results of treatment supported the superior efficacy of the 200-300 ng/ml and 350-450 ng/ml serum clozapine level ranges over the 50-150 ng/ml range, with no advantage for 350-450 ng/ml over 200-300 ng/ml. Sleepiness increased with increasing serum levels.

CONCLUSIONS

Serum clozapine levels per unit of daily dose were at the lower end of the range noted in previous reports, possibly reflecting the current study's dosing schedules of twice or three times a day, the 11- to 13-hour postdose sampling time, and the moderate doses given. Serum clozapine levels, if interpreted in relation to daily clozapine dosing schedules, postdose sampling time, and total daily dose, may help to guide dosing to provide adequate opportunities for therapeutic response and to limit certain side effects of clozapine treatment.

摘要

目的

本研究旨在确定血清氯氮平水平与治疗反应之间的关系。

方法

56名符合DSM-III-R慢性精神分裂症标准且对经典抗精神病药物延长治疗无反应的住院患者,被随机分配至三个血清水平范围之一,接受为期12周的氯氮平双盲治疗:低水平(50 - 150纳克/毫升)、中等水平(200 - 300纳克/毫升)或高水平(350 - 450纳克/毫升)。在患者停用常规抗精神病药物和抗胆碱能药物之前完成基线临床评估。在氯氮平治疗期间,每周测定血清水平,以便调整氯氮平剂量,使每位患者维持在其指定血清水平范围的中点附近。治疗6周和12周后完成临床评估。

结果

治疗结果分析支持血清氯氮平水平在200 - 300纳克/毫升和350 - 450纳克/毫升范围的疗效优于50 - 150纳克/毫升范围,350 - 450纳克/毫升范围并不优于200 - 300纳克/毫升范围。嗜睡随着血清水平升高而增加。

结论

每日单位剂量的血清氯氮平水平处于既往报道范围的下限,这可能反映了本研究每日两次或三次的给药方案、给药后11至13小时的采样时间以及给予的中等剂量。如果结合氯氮平每日给药方案、给药后采样时间和每日总剂量来解读血清氯氮平水平,可能有助于指导给药,以提供充分的治疗反应机会并限制氯氮平治疗的某些副作用。

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