Grover Sandeep, Singla Himanshu, Chakrabarti Subho, Avasthi Ajit
Department of Psychiatry, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Indian J Psychol Med. 2020 Mar 9;42(2):162-167. doi: 10.4103/IJPSYM.IJPSYM_269_19. eCollection 2020 Mar-Apr.
Little is known from India about the experience of using olanzapine long-acting antipsychotic injectables (LAI). In this background, this study aimed to evaluate the clinical profile of patients suffering from schizophrenia who were prescribed olanzapine LAI and to evaluate the usefulness and acceptability of olanzapine LAI among these patients.
In this retrospective study, data of all the patients with schizophrenia receiving olanzapine pamoate, was extracted.
40 patients (males-55%; mean [SD] age- 36.2 (12) years; mean duration of illness (SD) prior to depot-143.3 (115.9) months) were included in the study. Olanzapine LAI was invariably prescribed in patients with a past history of non-compliance. Data was available for a mean (SD) follow-up duration of 17 (10.8) months. The most frequently used dose of olanzapine LAI used was 300 mg every two weeks (55%). This was followed by 405 mg every four weeks in (32.5%). Mean Clinical Global Impression (CGI) Severity score prior to starting of olanzapine LAI was 5.8 (0.7), which reduced to 2.7 (1.1) at the time of last follow-up or the last use of olanzapine LAI, and this was a statistically significant improvement (paired -test value = 16.41; < 0.001). Only one (2.5%) patient experienced Post injection Delirium/Sedation Syndrome during the study period. Only one patient was hospitalized after starting depot olanzapine.
Olanzapine LAI is mostly used in patients with a history of non-compliance. Olanzapine LAI is associated with a significant reduction in the severity of illness.
在印度,关于使用奥氮平长效抗精神病注射剂(LAI)的经验知之甚少。在此背景下,本研究旨在评估接受奥氮平LAI治疗的精神分裂症患者的临床特征,并评估奥氮平LAI在这些患者中的有效性和可接受性。
在这项回顾性研究中,提取了所有接受帕莫酸奥氮平治疗的精神分裂症患者的数据。
40名患者(男性占55%;平均[标准差]年龄为36.2(12)岁;长效注射剂治疗前的平均病程[标准差]为143.3(115.9)个月)纳入研究。奥氮平LAI总是开给有不依从病史的患者。平均(标准差)随访时间为17(10.8)个月。最常用的奥氮平LAI剂量是每两周300毫克(55%)。其次是每四周405毫克(32.5%)。开始使用奥氮平LAI前的平均临床总体印象(CGI)严重程度评分为5.8(0.7),在最后一次随访或最后一次使用奥氮平LAI时降至2.7(1.1),这是具有统计学意义的改善(配对t检验值 = 16.41;P < 0.001)。在研究期间,只有一名(2.5%)患者出现注射后谵妄/镇静综合征。开始使用长效奥氮平后只有一名患者住院。
奥氮平LAI主要用于有不依从病史的患者。奥氮平LAI与疾病严重程度的显著降低有关。