Suppr超能文献

用棕榈酸帕利哌酮治疗近期病情加重的精神分裂症患者:疗效和耐受性的初步研究。

Treatment of Patients with Recently Exacerbated Schizophrenia with Paliperidone Palmitate: A Pilot Study of Efficacy and Tolerability.

作者信息

Gattaz Wagner F, Saracco-Alvarez Ricardo, Daltio Claudiane Salles, Van de Bilt Martinus T, Ortegón Jose Julian, Villaseñor-Bayardo Sergio J, Louzã Mario, Elkis Helio, Soares Bernardo, Cabrera Jaramillo Patricia, Lawson Fabio, Díaz-Galvis Leonardo

机构信息

Laboratory of Neuroscience (LIM27), Instituto de Psiquiatria do Hospital das Clinicas da Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.

Instituto Nacional de Psiquiatría Ramón de la Fuentel, México D.F., México.

出版信息

Neuropsychiatr Dis Treat. 2020 Sep 10;16:2063-2072. doi: 10.2147/NDT.S233537. eCollection 2020.

Abstract

BACKGROUND

Paliperidone palmitate is a long-acting, second-generation antipsychotic (SGA) indicated for the treatment of acute exacerbations and maintenance treatment of adults with schizophrenia. This study addressed the response to paliperidone palmitate in Latin American patients with acute symptoms and recently diagnosed schizophrenia.

OBJECTIVE

Explore the efficacy and tolerability of paliperidone palmitate administered once a month for 4 months in patients with acute phase and recent diagnosis (within 1-6 years) of schizophrenia in 3 Latin American countries.

METHODS

This was a non-randomized, open-label, multicenter study with paliperidone palmitate injected intramuscularly in the deltoid muscle at an initial loading dose of 150 mg eq. (234 mg) on day 1 and 100 mg eq. (156 mg) on day 8 (± 4 days). The recommended maintenance dose was 75 mg eq. (117 mg) from day 36 to day 92. Efficacy was evaluated with PANSS and CGI-S. The last observation carried forward (LOCF) was used for efficacy analysis for imputation of missing data; no adjustments were made for multiplicity. Adverse events were evaluated during treatment.

RESULTS

The patient retention rate was 84.0% (144 patients received study drug; 121 finished the study). The percentage of patients with a reduction of at least 30% in PANSS total score compared to baseline gradually increased during the study, and at the end, 78.4% of patients showed response. The PANSS total score and CGI-S scores decreased significantly from baseline to LOCF endpoint ( <0.0001 for both); significant reduction in PANSS total score was observed at day 8 and persisted to the end of the study. Most common adverse events were muscle rigidity (11.8%), akathisia (11.1%), injection-site pain (7.6%), weight gain (7.6%), and insomnia (7.6%).

CONCLUSION

Paliperidone palmitate was efficacious in Latin American patients studied with an acute exacerbation and recent diagnosis of schizophrenia, and no new safety signals were identified.

摘要

背景

棕榈酸帕利哌酮是一种长效第二代抗精神病药物(SGA),用于治疗成人精神分裂症的急性加重期及维持治疗。本研究探讨了棕榈酸帕利哌酮在拉丁美洲有急性症状且近期诊断为精神分裂症患者中的疗效。

目的

探讨在3个拉丁美洲国家中,急性期且近期诊断(1 - 6年)为精神分裂症的患者每月注射一次棕榈酸帕利哌酮,持续4个月的疗效和耐受性。

方法

这是一项非随机、开放标签的多中心研究,棕榈酸帕利哌酮通过肌肉注射至三角肌,第1天初始负荷剂量为150 mg当量(234 mg),第8天(±4天)为100 mg当量(156 mg)。推荐维持剂量为从第36天至第92天75 mg当量(117 mg)。采用阳性和阴性症状量表(PANSS)及临床总体印象量表 - 严重程度(CGI - S)评估疗效。末次观察结转(LOCF)用于缺失数据插补的疗效分析;未对多重性进行调整。治疗期间评估不良事件。

结果

患者保留率为84.0%(144例患者接受研究药物;121例完成研究)。与基线相比,PANSS总分至少降低30%的患者百分比在研究期间逐渐增加,最终,78.4%的患者显示有反应。从基线到LOCF终点,PANSS总分和CGI - S评分均显著降低(两者均<0.0001);在第8天观察到PANSS总分显著降低,并持续至研究结束。最常见的不良事件为肌肉强直(11.8%)、静坐不能(11.1%)、注射部位疼痛(7.6%)、体重增加(7.6%)和失眠(7.6%)。

结论

棕榈酸帕利哌酮在拉丁美洲急性加重期且近期诊断为精神分裂症的研究患者中有效,且未发现新的安全信号。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验