首页> 外文期刊>Progress in Neuro-Psychopharmacology & Biological Psychiatry: An International Research, Review and News Journal >Effectiveness, safety, and tolerability of ziprasidone for treating schizophrenia patients undergoing usual care: A 12-month, open-label, flexible-dose, naturalistic observational trial
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Effectiveness, safety, and tolerability of ziprasidone for treating schizophrenia patients undergoing usual care: A 12-month, open-label, flexible-dose, naturalistic observational trial

机译:齐拉西酮治疗接受常规护理的精神分裂症患者的有效性,安全性和耐受性:一项为期12个月的开放标签,灵活剂量,自然观察性试验

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Objective: This is a first report from a long-term study aimed to evaluate efficacy, safety, tolerability, cognitive functioning, and quality of life outcomes during ziprasidone treatment of chronic schizophrenia patients in the "real-world". Method: Seventy clinically unstable schizophrenia patients with persistent symptoms or troublesome side effects were assigned to a 12-month, open-label, flexible-dose (40-160 mg/day), large-scale, naturalistic trial. Outcome measures were taken at baseline, 6, and 12 months, and included the Positive and Negative Syndrome Scale-(PANSS), the Clinical Global Impression (CGI-S) scale, the Global Assessment of Functioning Scale (GAF) scores, treatment-emergent adverse events, body weight, and drug attitude. Results: Thirty-two patients fully completed the study protocol. A discontinuation of treatment for any cause occurred in 54.3% of patients; the mean time until discontinuation was 4.4+-2.7 months. A discontinuation due to lack of clinical efficacy was more predominantly linked to patient perception (25.7%) than to physicians' conclusions alone (8.6%), adverse events (11.4%), and other reasons (8.6%). After controlling daily dose of ziprasidone, concomitant medications and sex, ANCOVA revealed improvement in PANSS factors, and global functioning among patients who had completed the study. Improvement in PANSS and GAF dimensions was evident at a 6-month visit, and it continued until the endpoint. When a cutoff of 20% improvement of PANSS total scores was used, the response rate among completers was 43.8%. Most common side effects were: fatigue, sleep disturbances, and headache. Ziprasidone did not appear to be linked to weight gain. Conclusion: This study suggests that ziprasidone may be beneficial for long-term treatment of schizophrenia patients in terms of severity of symptoms, and general functioning. Ziprasidone is well tolerated during the long-term treatment of chronic schizophrenia patients undergoing usual care.
机译:目的:这是一项长期研究的第一份报告,旨在评估在“现实世界”中使用齐拉西酮治疗慢性精神分裂症患者的有效性,安全性,耐受性,认知功能和生活质量。方法:将70例具有持续症状或不良副作用的临床不稳定型精神分裂症患者纳入一项为期12个月的开放标签,剂量灵活(40-160 mg /天)的大型自然试验。在基线,第6和第12个月时采取了指标,包括阳性和阴性综合征量表(PANSS),临床总体印象量表(CGI-S)量表,功能评估的全局量表(GAF)评分,紧急不良事件,体重和药物态度。结果:32名患者完全完成了研究方案。 54.3%的患者因任何原因停止治疗;直到停药的平均时间为4.4 + -2.7个月。由于缺乏临床疗效而中断治疗与患者的知觉(25.7%)相比,主要与仅凭医生的结论(8.6%),不良事件(11.4%)和其他原因(8.6%)相关。在控制了齐拉西酮的日剂量,伴随的药物治疗和性别之后,ANCOVA揭示了PANSS因子的改善以及完成研究的患者的整体功能。在访问了6个月后,PANSS和GAF尺寸明显改善,并且一直持续到终点。当使用PANSS总分数提高20%作为截止值时,完成者的回应率为43.8%。最常见的副作用是:疲劳,睡眠障碍和头痛。 Ziprasidone似乎与体重增加无关。结论:这项研究表明,就症状的严重程度和总体功能而言,齐拉西酮对精神分裂症患者的长期治疗可能是有益的。在长期接受常规护理的精神分裂症患者的长期治疗过程中,齐普拉西酮的耐受性良好。

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