Smith R C, Baumgartner R, Shvartsburd A, Ravichandran G K, Vroulis G, Mauldin M
Psychopharmacology (Berl). 1985;85(4):449-55. doi: 10.1007/BF00429663.
The relative utility of steady-state (SS), plasma (Pl), and red blood cell (RBC) haloperidol levels for predicting clinical response was evaluated in a fixed-dose study in schizophrenic inpatients. There were significant curvilinear relationships between the decrease in BPRS Psychosis Factor Scores by day 24 of haloperidol treatment and both Pl (R2 = 0.34) and RBC (R2 = 0.38) haloperidol levels. Although SS RBC haloperidol levels consistently showed a slightly stronger relationship to clinical response than Pl levels in several comparisons, the differences in R2s between Pl and RBC haloperidol were not statistically significant. Ninety percent confidence intervals for the blood level ranges associated with optimal clinical response in our sample of patients were: 6.5-16.5 ng/ml Pl haloperidol and 2.2-6.8 ng/ml RBC haloperidol.
在一项针对精神分裂症住院患者的固定剂量研究中,评估了稳态(SS)、血浆(Pl)和红细胞(RBC)中氟哌啶醇水平对预测临床反应的相对效用。在氟哌啶醇治疗第24天时,简明精神病评定量表(BPRS)精神病因子评分的降低与血浆(R2 = 0.34)和红细胞(R2 = 0.38)氟哌啶醇水平之间存在显著的曲线关系。尽管在几次比较中,稳态红细胞氟哌啶醇水平与临床反应的关系始终略强于血浆水平,但血浆和红细胞氟哌啶醇水平的R2差异无统计学意义。在我们的患者样本中,与最佳临床反应相关的血药浓度范围的90%置信区间为:血浆氟哌啶醇6.5 - 16.5 ng/ml和红细胞氟哌啶醇2.2 - 6.8 ng/ml。