Benedetti Alessandra, Di Paolo Antonello, Lastella Marianna, Casamassima Francesco, Candiracci Chiara, Litta Antonella, Ciofi Laura, Danesi Romano, Lattanzi Lorenzo, Del Tacca Mario, Cassano Giovanni Battista
those Authors equally contributed to the study.
Clin Pract Epidemiol Ment Health. 2010 Jun 4;6:30-5. doi: 10.2174/1745017901006010030.
To evaluate the efficacy and safety of the augmentation of clozapine with aripiprazole in patients with treatment-resistant schizoaffective and psychotic bipolar disorders in a retrospective manner. Pharmacodynamic and pharmacokinetic interactions between the two drugs were also investigated.
Three men and 4 women (median age 36 and 40 years, respectively) who had mean scores at BPRS and CGI-Severity of 59.1+/-12.0 and 5.4+/-0.5, respectively, were treated with clozapine (mean dose 292.9+/-220.7 mg/day). Patients received an adjunctive treatment with aripiprazole (mean dose 6.8 +/- 3.7 mg/day). Clozapine, norclozapine and aripiprazole plasma levels were measured by means of a high performance liquid chromatograpy with UV detection.
Total scores at BPRS decreased significantly (from 59.1+/-12.0 to 51.1+/-15.6, p=0.007) after aripirazole augmentation. In particular, the factors "thought disorder" (from 10.4+/-4.4 to 9.0+/-4.5, p=.047) and "anergia" (from 10.0+/-2.7 to 8.0+/-2.4, p=.018) significantly improved. Concomitant administration of aripiprazole and clozapine did not result in an increase in side effects over the period of treatment. Dose-normalized plasma levels of both clozapine and norclozapine and the clozapine/norclozapine metabolic ratio in all patients did not vary as well.
The augmentation of clozapine with aripirazole was safe and effective in severe psychotic schizoaffective and bipolar disorders which failed to respond to atypical antipsychotics. A possible pharmacokinetic interaction between clozapine and aripiprazole does not account for the improved clinical benefit obtained after aripiprazole augmentation.
以回顾性方式评估阿立哌唑增强氯氮平治疗难治性分裂情感性障碍和精神病性双相情感障碍患者的疗效和安全性。同时研究两种药物之间的药效学和药代动力学相互作用。
3名男性和4名女性(年龄中位数分别为36岁和40岁),简明精神病评定量表(BPRS)平均得分59.1±12.0,临床总体印象量表严重程度(CGI-Severity)平均得分5.4±0.5,接受氯氮平治疗(平均剂量292.9±220.7毫克/天)。患者接受阿立哌唑辅助治疗(平均剂量6.8±3.7毫克/天)。采用高效液相色谱-紫外检测法测定氯氮平、去甲氯氮平和阿立哌唑的血浆水平。
阿立哌唑增强治疗后,BPRS总分显著降低(从59.1±12.0降至51.1±15.6,p = 0.007)。特别是,“思维紊乱”因子(从10.4±4.4降至9.0±4.5,p = 0.047)和“无动力”因子(从10.0±2.7降至8.0±2.4,p = 0.018)显著改善。在治疗期间,阿立哌唑与氯氮平联合使用未导致副作用增加。所有患者氯氮平和去甲氯氮平的剂量标准化血浆水平以及氯氮平/去甲氯氮平代谢率也未发生变化。
在对非典型抗精神病药物无反应的重度精神病性分裂情感性障碍和双相情感障碍中,阿立哌唑增强氯氮平治疗安全有效。氯氮平和阿立哌唑之间可能的药代动力学相互作用并不能解释阿立哌唑增强治疗后获得的临床益处改善情况。