Volavka J, Cooper T B, Czobor P, Meisner M
Nathan S. Kline Institute for Psychiatric Research, Orangeburg, NY, USA.
Arch Gen Psychiatry. 1995 Oct;52(10):837-45. doi: 10.1001/archpsyc.1995.03950220047010.
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.
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).
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.
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.
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。
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)。
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。
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。