Carmassi Claudia, Dell'Oste Valerio, Fantasia Sara, Bordacchini Andrea, Bertelloni Carlo Antonio, Scarpellini Pietro, Pedrinelli Virginia
Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Department of Biotechnology, Chemistry and Pharmacy, University of Siena, Siena, Italy.
Front Psychiatry. 2024 May 21;15:1382013. doi: 10.3389/fpsyt.2024.1382013. eCollection 2024.
Cariprazine, a third-generation antipsychotic (TGAs), has demonstrated efficacy in the treatment of schizophrenia with good tolerability profile. Actual real-world literature data are lacking, particularly when exploring its efficacy in the long term. The present study examined the effects of cariprazine treatment on specific psychopathological domains with a particular focus on outcomes and side effects in real-life experience, after a long-term treatment.
The present 12-month longitudinal naturalistic study included a sample of subjects with a DSM-5-TR diagnosis of schizophrenia, recruited in the outpatients' psychiatric services of university and community hospitals in Italy, naturally treated with cariprazine. The assessments included: a sociodemographic data sheet, the Structured Clinical Interview for the DSM-5 (SCID-5), the Positive and Negative Symptom Scale (PANSS) and the St. Hans Rating Scale (SHRS). The PANSS was also administered after 6 (T1) and 12 (T2) months of treatment with cariprazine while the SHRS at T1.
The total sample consisted of 31 patients, 15 males and 16 females. A significant decrease of the PANSS' subscales, Marder factors and total mean scores emerged at both T1 and T2 with respect to T0. Extrapyramidal symptoms occurred in a minority of patients and in mild or mild/moderate forms: no patient showed moderate forms of psychic/motor akathisia or dystonia, three subjects showed moderate parkinsonism.
This study confirms a good efficacy profile of cariprazine in both positive and negative symptoms in patients with Schizophrenia, combined with a good tolerability profile in extrapyramidal symptoms.
卡立哌嗪是一种第三代抗精神病药物(TGA),已证明在治疗精神分裂症方面有效,且耐受性良好。目前缺乏实际的真实世界文献数据,尤其是在探索其长期疗效时。本研究考察了卡立哌嗪治疗对特定精神病理学领域的影响,特别关注长期治疗后的实际生活中的疗效和副作用。
本为期12个月的纵向自然主义研究纳入了一组经DSM-5-TR诊断为精神分裂症的受试者样本,这些受试者在意大利大学和社区医院的门诊精神科接受卡立哌嗪自然治疗。评估包括:一份社会人口数据表、DSM-5结构化临床访谈(SCID-5)、阳性和阴性症状量表(PANSS)以及圣汉斯评定量表(SHRS)。在使用卡立哌嗪治疗6个月(T1)和12个月(T2)后也进行了PANSS评估,而SHRS在T1时进行评估。
总样本包括31名患者,15名男性和16名女性。与T0相比,在T1和T2时,PANSS各分量表、马德因子和总平均分均显著下降。锥体外系症状发生在少数患者中,且为轻度或轻度/中度形式:没有患者表现出中度形式的精神/运动性静坐不能或肌张力障碍,三名受试者表现出中度帕金森症。
本研究证实卡立哌嗪对精神分裂症患者的阳性和阴性症状均具有良好的疗效,同时对锥体外系症状具有良好的耐受性。