Kirch D G, Bigelow L B, Korpi E R, Wagner R L, Zalcman S, Wyatt R J
Neuropsychiatry Branch, NIMH, Neuropsychiatric Research Hospital at Saint Elizabeths, Washington, DC 20032.
Schizophr Bull. 1988;14(2):283-9. doi: 10.1093/schbul/14.2.283.
Previous studies have reported a therapeutic window (i.e., a curvilinear relationship between clinical response and drug level) for haloperidol concentrations in serum or plasma. The authors treated 30 acutely decompensated schizophrenic inpatients with a fixed dose of haloperidol (.4 mg/kg/day). After 6 weeks there was no statistically significant correlation between clinical improvement and serum haloperidol concentration. Fifteen subjects with serum concentrations of 5-15 ng/ml did not differ in clinical improvement compared with 15 subjects who had concentrations above 15 ng/ml. These data are consistent with a therapeutic plateau, rather than a window, and suggest that in most cases there is no clinical advantage to the use of haloperidol doses greater than approximately 30 mg/day in schizophrenic patients.
先前的研究报道了血清或血浆中氟哌啶醇浓度的治疗窗(即临床反应与药物水平之间的曲线关系)。作者用固定剂量的氟哌啶醇(0.4毫克/千克/天)治疗了30名急性失代偿的精神分裂症住院患者。6周后,临床改善与血清氟哌啶醇浓度之间无统计学显著相关性。血清浓度为5 - 15纳克/毫升的15名受试者与浓度高于15纳克/毫升的15名受试者在临床改善方面没有差异。这些数据与治疗平台期而非治疗窗一致,表明在大多数情况下,精神分裂症患者使用大于约30毫克/天的氟哌啶醇剂量并无临床优势。