Rama Raj Palaniraj, Lewis Matthew, Macfarlane Stephen
Monash University, Clayton, Victoria, Australia.
Department of Aged Psychiatry, Caulfield Hospital, Caulfield, Victoria, Australia.
BMJ Case Rep. 2015 Aug 26;2015:bcr2015212149. doi: 10.1136/bcr-2015-212149.
We present detailed data on the efficacy and safety profile of paliperidone palmitate once-monthly long acting injectable (PP1M-LAI) in the treatment of schizophrenia in an elderly Caucasian woman. PP1M-LAI was initiated with starting doses of 150 and 100 mg on treatment days 1 and 8, respectively. Subsequent 100 mg doses of PP1M-LAI were then administered at 4-weekly intervals. The primary efficacy variable was the change in Positive and Negative Syndrome Scale (PANSS) total score from baseline. Safety assessment variables included assessment of treatment emergent adverse events, clinical laboratory tests, vital sign measurements, ECG, Calgary Depression Scale for Schizophrenia (CDSS), mini-mental status examination, Abnormal Involuntary Movement Scale (AIMS), Barnes Akathisia Rating Scale (BARS), Simpson-Angus Scale for the Assessment of Extrapyramidal Side Effects (SAS) and WHO Quality of Life-BREF (WHO-QOL-BREF). The aforementioned variables were all monitored for changes from baseline over a period of 28 weeks. A reduction of PANSS total score was noted over the 28 weeks, demonstrating the efficacy of PP1M-LAI for the treatment of schizophrenia in our patient. Improvements were also noted in the BARS score, SAS score and WHO-QOL-BREF. Negative findings were observed with regard to several pre-established safety variables such as blood glucose levels, prolactin levels, QTC intervals and weight. Overall, the addition of PP1M-LAI to the treatment regime improved the control of psychotic symptoms. However, iatrogenic consequences arising from the use of PP1M-LAI need to be considered and balanced against the primary efficacy of the medication.
我们展示了关于棕榈酸帕利哌酮每月一次长效注射剂(PP1M-LAI)治疗一名老年白人女性精神分裂症的疗效和安全性的详细数据。PP1M-LAI分别在治疗第1天和第8天以150毫克和100毫克的起始剂量开始使用。随后每隔4周给予100毫克的PP1M-LAI剂量。主要疗效变量是阳性和阴性症状量表(PANSS)总分相对于基线的变化。安全性评估变量包括对治疗中出现的不良事件的评估、临床实验室检查、生命体征测量、心电图、精神分裂症卡尔加里抑郁量表(CDSS)、简易精神状态检查、异常不自主运动量表(AIMS)、巴恩斯静坐不能评定量表(BARS)、用于评估锥体外系副作用的辛普森-安格斯量表(SAS)以及世界卫生组织生活质量简表(WHO-QOL-BREF)。在28周的时间里,对上述所有变量相对于基线的变化进行了监测。在28周内观察到PANSS总分有所降低,证明了PP1M-LAI对我们患者精神分裂症的治疗效果。BARS评分、SAS评分和WHO-QOL-BREF也有改善。在一些预先设定的安全变量方面,如血糖水平、催乳素水平、QTC间期和体重,观察到了阴性结果。总体而言,在治疗方案中添加PP1M-LAI改善了对精神病症状的控制。然而,使用PP1M-LAI产生的医源性后果需要加以考虑,并与该药物的主要疗效进行权衡。