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精神分裂症和分裂情感性障碍患者的血浆氟哌啶醇水平及临床疗效

Plasma haloperidol levels and clinical effects in schizophrenia and schizoaffective disorder.

作者信息

Volavka J, Cooper T B, Czobor P, Meisner M

机构信息

Nathan S. Kline Institute for Psychiatric Research, Orangeburg, NY, USA.

出版信息

Arch Gen Psychiatry. 1995 Oct;52(10):837-45. doi: 10.1001/archpsyc.1995.03950220047010.

Abstract

BACKGROUND

Plasma haloperidol levels between 5 and 11 ng/mL may be clinically optimal for acutely exacerbated schizophrenia, but the evidence for this therapeutic window has been inconsistent.

METHODS

Haloperidol was administered in a double-blind manner during two consecutive 3-week experimental periods to 65 patients with acutely exacerbated schizophrenia or schizoaffective disorder. Two plasma levels were targeted: "low" (2 ng/mL) and "moderate" (10 ng/mL). The subjects were randomly assigned to four treatment sequences (low-low, low-moderate, moderate-moderate, or moderate-low).

RESULTS

In the first 3 weeks, the antipsychotic efficacy of haloperidol increased with plasma levels up to approximately 12 ng/mL. In the second 3 weeks, decrease of plasma levels reduced negative symptoms.

CONCLUSION

For most patients, plasma levels not exceeding 12 ng/mL yield the best results in the first 3 weeks of treatment. Subsequent lowering of the plasma levels may improve negative symptoms.

摘要

背景

对于急性加重型精神分裂症,血浆中氟哌啶醇水平在5至11纳克/毫升之间可能在临床上最为理想,但这一治疗窗的证据并不一致。

方法

在两个连续的为期3周的实验期内,以双盲方式对65例急性加重型精神分裂症或分裂情感性障碍患者给予氟哌啶醇。设定了两个血浆水平目标:“低”(2纳克/毫升)和“中”(10纳克/毫升)。受试者被随机分配到四个治疗序列(低-低、低-中、中-中或中-低)。

结果

在最初3周内,氟哌啶醇的抗精神病疗效随着血浆水平升高至约12纳克/毫升而增强。在第二个3周内,血浆水平降低减轻了阴性症状。

结论

对于大多数患者,在治疗的前3周,血浆水平不超过12纳克/毫升可产生最佳效果。随后降低血浆水平可能会改善阴性症状。

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