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抗精神病药物在儿科患者中的安全性和耐受性:一项为期1年的自然主义研究数据。

Safety and Tolerability of Antipsychotic Drugs in Pediatric Patients: Data From a 1-Year Naturalistic Study.

作者信息

Cicala Giuseppe, Barbieri Maria A, Santoro Vincenza, Tata Carmela, Colucci Pia V, Vanadia Francesca, Drago Flavia, Russo Carmelita, Cutroneo Paola M, Gagliano Antonella, Spina Edoardo, Germanò Eva

机构信息

Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.

Childhood and Adolescence Neuropsychiatry, Azienda Sanitaria Provinciale 8, Syracuse, Italy.

出版信息

Front Psychiatry. 2020 Mar 24;11:152. doi: 10.3389/fpsyt.2020.00152. eCollection 2020.

Abstract

Antipsychotic drugs (APs) are increasingly used to treat a variety of psychiatric disorders in children and adolescents. However, their safety and tolerability profiles, when used in a developmental age context, show different characteristics from the ones observed in adult patients. Treatment with APs in pediatric patients is often long-term. However, the tolerability data regarding these patients mostly derive from short-term studies. Starting from April 2017, for a 1-year period, patients between 4 and 18 years of age followed by five units of developmental age neuropsychiatry, who initiated a treatment with at least an AP (ATC class N05A) were included into the study. Patient-related data have been collected at baseline and regularly thereafter, as allowed by the clinical routine. Changes to continuous variables over time have been analyzed using a linear mixed model in subsamples of our population treated with risperidone or aripiprazole. During the observation period, 158 patients were initially enrolled, but only 116 completed 12 months of therapy with an AP. Risperidone was the most used AP ( = 52) followed by aripiprazole ( = 44) and olanzapine ( = 7). For both the aripiprazole and risperidone groups, the mean body mass index (BMI) ( < 0.001 for both groups) and heart rate ( = 0.026 for aripiprazole group and < 0.001 for the risperidone one) values significantly increased over time. The mean prolactin concentration value significantly increased over time only in the risperidone group ( = 0.04). Eighty-six patients experienced at least one adverse drug reaction (ADR), accounting for a total of 238 specific reactions, with the most frequent being weight gain ( = 34), increased serum prolactin levels ( = 21), hyperphagia ( = 20), and hypercholesterolemia ( = 14). Among these, only 24 ADRs were classifiable as serious. The results of this study confirm that risperidone and aripiprazole are relatively well-tolerated therapeutic options for the treatment of a variety of psychiatric disorders in pediatric patients. However, in findings such as statistically significant increments of BMI and heart rate mean values, the variations over time in prolactin levels observed with risperidone and the differences between the two drugs remark the necessity of systematic monitoring.

摘要

抗精神病药物(APs)越来越多地用于治疗儿童和青少年的各种精神疾病。然而,在发育年龄背景下使用时,它们的安全性和耐受性特征与成年患者中观察到的不同。儿科患者使用APs进行治疗通常是长期的。然而,关于这些患者的耐受性数据大多来自短期研究。从2017年4月开始,为期1年,纳入了4至18岁、由五个发育年龄神经精神病学单位随访、开始使用至少一种AP(ATC分类N05A)进行治疗的患者。在临床常规允许的情况下,在基线时以及此后定期收集患者相关数据。使用线性混合模型对接受利培酮或阿立哌唑治疗的人群子样本中连续变量随时间的变化进行了分析。在观察期内,最初纳入了158名患者,但只有116名患者完成了12个月的AP治疗。利培酮是使用最多的AP(n = 52),其次是阿立哌唑(n = 44)和奥氮平(n = 7)。对于阿立哌唑组和利培酮组,平均体重指数(BMI)(两组均P < 0.001)和心率(阿立哌唑组P = 0.026,利培酮组P < 0.001)值随时间显著增加。仅在利培酮组中,平均催乳素浓度值随时间显著增加(P = 0.04)。86名患者经历了至少一种药物不良反应(ADR),共计238种特定反应,最常见的是体重增加(n = 34)、血清催乳素水平升高(n = 21)、食欲亢进(n = 20)和高胆固醇血症(n = 14)。其中,只有24种ADR可归类为严重不良反应。本研究结果证实,利培酮和阿立哌唑对于治疗儿科患者的各种精神疾病是耐受性相对良好的治疗选择。然而,在BMI和心率平均值有统计学显著增加、利培酮观察到的催乳素水平随时间变化以及两种药物之间的差异等研究结果中,表明了系统监测的必要性。

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