Potanin S S, Burminskiy D S, Morozova M A, Platova A I, Baymeeva N V, Miroshnichenko I I
Mental Health Research Centre, Moscow, Russia.
Zh Nevrol Psikhiatr Im S S Korsakova. 2015;115(11):40-46. doi: 10.17116/jnevro201511511140-46.
To study a relationship between plasma levels of antipsychotics (AP) and severity of side-effects (SE) during the treatment of inpatients with exacerbation of schizophrenia.
The study included 39 patients treated with risperidone, haloperidol, zuclopenthixol, clozapine, aripiprazole or olanzapine as monotherapy or in combination of two AP. Blood sampling to measure the AP plasma level was performed twice (at 7-10 and 26-30 day from start of treatment), the levels of prolactin and glucose were determined once (at 26-30 day from start of treatment). Patients were assessed by psychometric scales PANSS and NSA and the side-effects scale UKU.
The increased concentration of AP was noted in 33% of the patients. The high concentration of AP was significantly associated with akathisia and hyperkinesia (by UKU scale), NSA retardation factor and hyperprolactinemia. Patients with severe hyperprolactinemia were twice as likely to have a clinically significant depression. Increased blood glucose levels were observed in 18% of the patients, there was no significant association with AP plasma levels. Mental SE were most prominent, with a drift towards the neurological SE in the group with higher AP plasma levels. Chlorpromazine equivalent didn't significantly differ in the groups with normal, high and low AP concentrations.
Elevated AP plasma levels, which were associated with some clinically significant SE and some negative symptoms, were found in most patients. In this regard, therapeutic drug monitoring is a promising method for the individualization of schizophrenia exacerbation treatment in routine clinical practice.
研究精神分裂症急性加重期住院患者治疗期间抗精神病药物(AP)血浆水平与副作用(SE)严重程度之间的关系。
该研究纳入了39例接受利培酮、氟哌啶醇、氯噻吨、氯氮平、阿立哌唑或奥氮平单药治疗或两种抗精神病药物联合治疗的患者。在治疗开始后的第7 - 10天和第26 - 30天进行两次采血以测量抗精神病药物血浆水平,在治疗开始后的第26 - 30天测定一次催乳素和血糖水平。通过心理测量量表PANSS和NSA以及副作用量表UKU对患者进行评估。
33%的患者抗精神病药物浓度升高。抗精神病药物高浓度与静坐不能和运动亢进(根据UKU量表)、NSA迟缓因子及高催乳素血症显著相关。严重高催乳素血症患者出现具有临床意义的抑郁症的可能性是正常人的两倍。18%的患者血糖水平升高,与抗精神病药物血浆水平无显著关联。精神副作用最为突出,在抗精神病药物血浆水平较高的组中倾向于出现神经副作用。氯丙嗪等效剂量在抗精神病药物浓度正常、高和低的组中无显著差异。
大多数患者存在抗精神病药物血浆水平升高的情况,这与一些具有临床意义的副作用和一些阴性症状相关。在这方面,治疗药物监测是常规临床实践中精神分裂症急性加重期治疗个体化的一种有前景的方法。