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Efficacy and Safety Profile of Risperidone Long-acting Injection in Adolescents in a Real-life Setting

机译:利培酮长效注射剂在现实生活中对青少年的疗效和安全性

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Objective Risperidone long-acting injection (RLAI) was shown to be an alternative option in adult patients, but there is not available data in child and adolescents about this medication. The aim of this study is to evaluate the safety and efficiency profile of RLAI in a group of adolescents. Methods Eleven cases with conduct disorder and severe aggressive behaviors were initiated treatment with risperidone oral form. All cases were then shifted to RLAI 25 mg injection in each 15 days due to poor compliance to oral risperidone treatment. Efficiency of treatment included indicators of clinical severity and improvement, which were evaluated by Clinical Global Impression-Severity (CGI-S) and Improvement (CGI-I). Safety evaluation was performed by using Extrapyramidal Symptoms Rating Scale, and by monitoring body weight. Follow-up visits were done at the treatment initiation, and 8th, 16th, and 24th weeks of first injection. Results Study included 9 girls, and 2 boys, with a mean age of 14.9±1.0 years. The CGI-S scores decreased from 6.6±0.5 at the beginning to 2.2±1.1 at the last visit ( p <0.001), which is a very significant decrease through better clinical level. The CGI-I scores were also improved significantly from 2.4±0.5 to 1.9±0.5 at 24th week ( p =0.001). Safety parameters were also showed favorable results, which there was no significant weight gain ( p =0.076), and well-tolerated extrapyramidal adverse effects. Conclusion Our results showed that RLAI is an efficient and safe medication option in the treatment of psychiatric disorders and severe behavioral problems in adolescents with low-compliance to oral treatment in our cases.
机译:目的利培酮长效注射剂(RLAI)被证明是成年患者的另一种选择,但尚无有关儿童和青少年的药物资料。这项研究的目的是评估RLAI在一群青少年中的安全性和有效性。方法对11例行为障碍和严重攻击行为的患者进行利培酮口服治疗。由于对利培酮口服治疗的依从性差,所有病例每15天转入RLAI 25 mg注射。治疗效率包括临床严重性和改善的指标,并通过临床总体印象严重度(CGI-S)和改善(CGI-1)进行了评估。通过使用锥体外系症状评定量表并通过监测体重来进行安全性评估。在治疗开始以及首次注射的第8、16和24周进行随访。结果研究包括9名女孩和2名男孩,平均年龄为14.9±1.0岁。 CGI-S评分从开始时的6.6±0.5降低到最后一次就诊时的2.2±1.1(p <0.001),这通过更好的临床水平是非常显着的。 CGI-I评分在第24周时也从2.4±0.5显着提高到1.9±0.5(p = 0.001)。安全性参数也显示出令人满意的结果,没有明显的体重增加(p = 0.076),并且锥体束外不良反应耐受性良好。结论我们的结果表明,RLAI是治疗精神病和严重行为问题的青少年的有效且安全的药物选择,我们本例的口服治疗依从性较低。

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