Absence of Change in Corrected QT Interval in Children and Adolescents Receiving Antipsychotic Treatment: A 12 Month Study

Prescriptions of antipsychotic drugs (AP) in children and adolescents have significantly increased in Europe as well as in the United States. However, there is limited evidence of the cardiac safety of second-generation antipsychotics (SGA) in the pediatric population. The aim of the study is to eva...

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Veröffentlicht in:Journal of child and adolescent psychopharmacology 2016-06, Vol.26 (5), p.449-457
Hauptverfasser: Alda, José A, Muñoz-Samons, Daniel, Tor, Jordina, Merchán-Naranjo, Jessica, Tapia-Casellas, Cecilia, Baeza, Inmaculada, Calvo-Escalona, Rosa, Castro-Fornieles, Josefina, Martínez-Cantarero, Carmen, Andrés-Nestares, Patricia, Fernández-Avilés, Francisco, Arango, Celso
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container_end_page 457
container_issue 5
container_start_page 449
container_title Journal of child and adolescent psychopharmacology
container_volume 26
creator Alda, José A
Muñoz-Samons, Daniel
Tor, Jordina
Merchán-Naranjo, Jessica
Tapia-Casellas, Cecilia
Baeza, Inmaculada
Calvo-Escalona, Rosa
Castro-Fornieles, Josefina
Martínez-Cantarero, Carmen
Andrés-Nestares, Patricia
Fernández-Avilés, Francisco
Arango, Celso
description Prescriptions of antipsychotic drugs (AP) in children and adolescents have significantly increased in Europe as well as in the United States. However, there is limited evidence of the cardiac safety of second-generation antipsychotics (SGA) in the pediatric population. The aim of the study is to evaluate the cardiac side effects of SGA in children and adolescents, and how they are influenced by clinical, demographic, and treatment factors. This article presents a naturalistic, longitudinal, multicenter study conducted in 216 treatment-naïve or quasi-naïve children and adolescents receiving AP treatment. It analyzed the possible influence of AP treatment on variables such as corrected QT (QTc) intervals and heart rate for a period of 12 months (baseline, 3 months, 6 months, and 12 months). Differences among the three main prescribed drugs used in the sample (risperidone, quetiapine, and olanzapine) were assessed. A total of 211 received one of the three most prescribed AP (quetiapine, risperidone or olanzapine). There were no significant QTc variations in the sample during follow-up (p = 0.54). There were no differences in QTc rates between the different SGA (risperidone-olanzapine p = 0.43; risperidone-quetiapine p = 0.42; olanzapine-quetiapine p = 0.23). When demographic, clinical, or concomitant treatment variables were considered, only baseline overweight correlated with QTc prolongation (p = 0.003). The heart rate in the whole sample tended to decrease during follow-up (p = 0.054). However, patients on quetiapine showed increased heart rate compared with those on risperidone (p = 0.04). In this sample, SGA seem to have a safe heart side effect profile in the child and adolescent population. There was no observed mean increase in QTc or in heart rate.
doi_str_mv 10.1089/cap.2015.0151
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However, there is limited evidence of the cardiac safety of second-generation antipsychotics (SGA) in the pediatric population. The aim of the study is to evaluate the cardiac side effects of SGA in children and adolescents, and how they are influenced by clinical, demographic, and treatment factors. This article presents a naturalistic, longitudinal, multicenter study conducted in 216 treatment-naïve or quasi-naïve children and adolescents receiving AP treatment. It analyzed the possible influence of AP treatment on variables such as corrected QT (QTc) intervals and heart rate for a period of 12 months (baseline, 3 months, 6 months, and 12 months). Differences among the three main prescribed drugs used in the sample (risperidone, quetiapine, and olanzapine) were assessed. A total of 211 received one of the three most prescribed AP (quetiapine, risperidone or olanzapine). There were no significant QTc variations in the sample during follow-up (p = 0.54). There were no differences in QTc rates between the different SGA (risperidone-olanzapine p = 0.43; risperidone-quetiapine p = 0.42; olanzapine-quetiapine p = 0.23). When demographic, clinical, or concomitant treatment variables were considered, only baseline overweight correlated with QTc prolongation (p = 0.003). The heart rate in the whole sample tended to decrease during follow-up (p = 0.054). However, patients on quetiapine showed increased heart rate compared with those on risperidone (p = 0.04). In this sample, SGA seem to have a safe heart side effect profile in the child and adolescent population. 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There were no differences in QTc rates between the different SGA (risperidone-olanzapine p = 0.43; risperidone-quetiapine p = 0.42; olanzapine-quetiapine p = 0.23). When demographic, clinical, or concomitant treatment variables were considered, only baseline overweight correlated with QTc prolongation (p = 0.003). The heart rate in the whole sample tended to decrease during follow-up (p = 0.054). However, patients on quetiapine showed increased heart rate compared with those on risperidone (p = 0.04). In this sample, SGA seem to have a safe heart side effect profile in the child and adolescent population. 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However, there is limited evidence of the cardiac safety of second-generation antipsychotics (SGA) in the pediatric population. The aim of the study is to evaluate the cardiac side effects of SGA in children and adolescents, and how they are influenced by clinical, demographic, and treatment factors. This article presents a naturalistic, longitudinal, multicenter study conducted in 216 treatment-naïve or quasi-naïve children and adolescents receiving AP treatment. It analyzed the possible influence of AP treatment on variables such as corrected QT (QTc) intervals and heart rate for a period of 12 months (baseline, 3 months, 6 months, and 12 months). Differences among the three main prescribed drugs used in the sample (risperidone, quetiapine, and olanzapine) were assessed. A total of 211 received one of the three most prescribed AP (quetiapine, risperidone or olanzapine). There were no significant QTc variations in the sample during follow-up (p = 0.54). There were no differences in QTc rates between the different SGA (risperidone-olanzapine p = 0.43; risperidone-quetiapine p = 0.42; olanzapine-quetiapine p = 0.23). When demographic, clinical, or concomitant treatment variables were considered, only baseline overweight correlated with QTc prolongation (p = 0.003). The heart rate in the whole sample tended to decrease during follow-up (p = 0.054). However, patients on quetiapine showed increased heart rate compared with those on risperidone (p = 0.04). In this sample, SGA seem to have a safe heart side effect profile in the child and adolescent population. There was no observed mean increase in QTc or in heart rate.</abstract><cop>United States</cop><pub>Mary Ann Liebert, Inc</pub><pmid>26779966</pmid><doi>10.1089/cap.2015.0151</doi><tpages>9</tpages></addata></record>
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subjects Adolescent
Antipsychotic Agents - adverse effects
Antipsychotic Agents - therapeutic use
Benzodiazepines - adverse effects
Benzodiazepines - therapeutic use
Biomarkers, Pharmacological
Child
Child, Preschool
Children & youth
Drug therapy
Electrocardiography - drug effects
Female
Heart Rate - drug effects
Humans
Long QT Syndrome - chemically induced
Long QT Syndrome - diagnosis
Longitudinal Studies
Male
Pediatrics
Prospective Studies
Quetiapine Fumarate - adverse effects
Quetiapine Fumarate - therapeutic use
Risperidone - adverse effects
Risperidone - therapeutic use
Studies
title Absence of Change in Corrected QT Interval in Children and Adolescents Receiving Antipsychotic Treatment: A 12 Month Study
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