Palao D J, Arauxo A, Brunet M, Bernardo M, Haro J M, Ferrer J, Gonzalez-Monclus E
Department of Psychiatry, Hospital Clínic i Provincial, Barcelona, Spain.
J Clin Psychopharmacol. 1994 Oct;14(5):303-10.
Twenty-two schizophrenic inpatients were treated for 3 weeks with three randomly fixed oral doses of haloperidol (10, 20, or 30 mg). Analysis of the results by a nonlinear regression model revealed a curvilinear relationship between haloperidol levels in plasma and clinical response, as assessed on the Brief Psychiatric Rating Scale (pseudo-R2 = 0.85, F = 17.7, p < 0.001, correlation between coefficients ranged from 0.99 to -0.52). This curve defines roughly three drug level ranges (low, < 5.5 ng/ml; optimal, 5.5 to 14.4 ng/ml; and high or toxic, > 14.4 ng/ml), which are significant for clinical practice. Patients with high levels improve to a lesser extent or even worsen in negative symptoms, showing a nonstatistically significant trend to present more extrapyramidal symptoms. Our data thus support the existence of a therapeutic window for haloperidol. Schizophrenic patients with acute exacerbation and drug levels in this range would have a greater probability of global clinical improvement.
22名精神分裂症住院患者接受了为期3周的治疗,随机给予三种固定口服剂量的氟哌啶醇(10毫克、20毫克或30毫克)。通过非线性回归模型对结果进行分析发现,血浆中氟哌啶醇水平与临床反应之间存在曲线关系,这是根据简明精神病评定量表评估得出的(伪R2 = 0.85,F = 17.7,p < 0.001,系数之间的相关性范围为0.99至 -0.52)。该曲线大致定义了三个药物水平范围(低水平,< 5.5纳克/毫升;最佳水平,5.5至14.4纳克/毫升;高水平或中毒水平,> 14.4纳克/毫升),这对临床实践具有重要意义。高水平患者的阴性症状改善程度较小甚至恶化,出现更多锥体外系症状的趋势无统计学意义。因此,我们的数据支持氟哌啶醇存在治疗窗这一观点。急性加重且药物水平处于该范围内的精神分裂症患者实现整体临床改善的可能性更大。