Psychosis Centre, Department of Psychiatry and Psychotherapy, Centre for Psychosocial Medicine, University Medical Center Hamburg-Eppendorf Hamburg, Martinistreet 52, 20246 Hamburg, Germany.
Eur Psychiatry. 2010 May;25(4):220-9. doi: 10.1016/j.eurpsy.2009.09.001. Epub 2009 Nov 18.
To measure symptomatic and functional remission in patients treated with risperidone long-acting injectable (RLAI).
Stable patients with psychotic disorders requiring medication change were switched to open-label RLAI in the switch to risperidone microspheres (StoRMi) trial. In this post-hoc analysis of the trial extension, follow-up was <or=18 months. Symptomatic remission was based on improvement in positive and negative syndrome scale (PANSS) scores and global remission (best outcome) was based on symptomatic remission, functional level, and mental-health quality of life. Predictive factors were evaluated.
Among 529 patients from seven European countries, mean participation duration was 358.7+/-232.4 days, with 18 months completed by 39.9% of patients. Symptomatic remission lasting >or=6 months occurred at some point during treatment in 33% of patients; predictors included comorbid disease, country, baseline symptom severity, baseline functioning, type of antipsychotic before switching, and duration of untreated psychosis. Best outcome occurred in 21% of patients; predictors included baseline symptom severity, baseline functioning, country, schizophrenia type, and early positive treatment course.
One in three patients with stable schizophrenia switching to RLAI experienced symptomatic remission, with combined symptomatic, functional, and quality-of-life remission in one in five patients. Symptomatic remission was predicted by better baseline symptom severity and country of origin, with a significantly greater likelihood of remission occurring among patients in Estonia/Slovenia compared with Portugal. Relapse was predicted by higher mode doses of RLAI, additional use of psychoactive medications, male gender, and country of origin, with relapse occurring most frequently in France and least frequently in Portugal. RLAI dose, additional use of psychoactive medications, and country of origin predicted best outcome, with best outcome occurring most frequently in Estonia/Slovenia and least frequently in Portugal.
评估利培酮长效注射剂(RLAI)治疗患者的症状和功能缓解情况。
在 Switch to risperidone microspheres(StoRMi)试验中,需要换药的精神障碍稳定患者转为开放性 RLAI 治疗。本试验扩展的事后分析中,随访时间<或=18 个月。症状缓解基于阳性和阴性综合征量表(PANSS)评分的改善,总缓解(最佳结局)基于症状缓解、功能水平和心理健康生活质量。评估了预测因素。
在来自 7 个欧洲国家的 529 例患者中,平均参与时间为 358.7+/-232.4 天,18 个月时完成的患者占 39.9%。33%的患者在治疗过程中的某个时间点出现持续>或=6 个月的症状缓解;预测因素包括合并疾病、国家、基线症状严重程度、基线功能、转换前的抗精神病药物类型和未治疗精神病的持续时间。21%的患者出现最佳结局;预测因素包括基线症状严重程度、基线功能、国家、精神分裂症类型和早期积极治疗过程。
在转换为 RLAI 的稳定精神分裂症患者中,有 1/3 的患者出现症状缓解,1/5 的患者出现症状、功能和生活质量联合缓解。症状缓解的预测因素是更好的基线症状严重程度和原籍国,与葡萄牙相比,爱沙尼亚/斯洛文尼亚的患者缓解可能性显著更高。复发的预测因素是 RLAI 的更高模式剂量、额外使用精神活性药物、男性和原籍国,法国的复发频率最高,葡萄牙的复发频率最低。RLAI 剂量、额外使用精神活性药物和原籍国预测最佳结局,与葡萄牙相比,爱沙尼亚/斯洛文尼亚的最佳结局发生频率更高。