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 |
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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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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.</description><identifier>ISSN: 1044-5463</identifier><identifier>EISSN: 1557-8992</identifier><identifier>DOI: 10.1089/cap.2015.0151</identifier><identifier>PMID: 26779966</identifier><language>eng</language><publisher>United States: Mary Ann Liebert, Inc</publisher><subject>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</subject><ispartof>Journal of child and adolescent psychopharmacology, 2016-06, Vol.26 (5), p.449-457</ispartof><rights>(©) Copyright 2016, Mary Ann Liebert, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c354t-d003027125e6b0a661a33d16dedf502c6b316c6d2763ec7ff7df951282b300fa3</citedby><cites>FETCH-LOGICAL-c354t-d003027125e6b0a661a33d16dedf502c6b316c6d2763ec7ff7df951282b300fa3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27907,27908</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26779966$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Alda, José A</creatorcontrib><creatorcontrib>Muñoz-Samons, Daniel</creatorcontrib><creatorcontrib>Tor, Jordina</creatorcontrib><creatorcontrib>Merchán-Naranjo, Jessica</creatorcontrib><creatorcontrib>Tapia-Casellas, Cecilia</creatorcontrib><creatorcontrib>Baeza, Inmaculada</creatorcontrib><creatorcontrib>Calvo-Escalona, Rosa</creatorcontrib><creatorcontrib>Castro-Fornieles, Josefina</creatorcontrib><creatorcontrib>Martínez-Cantarero, Carmen</creatorcontrib><creatorcontrib>Andrés-Nestares, Patricia</creatorcontrib><creatorcontrib>Fernández-Avilés, Francisco</creatorcontrib><creatorcontrib>Arango, Celso</creatorcontrib><title>Absence of Change in Corrected QT Interval in Children and Adolescents Receiving Antipsychotic Treatment: A 12 Month Study</title><title>Journal of child and adolescent psychopharmacology</title><addtitle>J Child Adolesc Psychopharmacol</addtitle><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.</description><subject>Adolescent</subject><subject>Antipsychotic Agents - adverse effects</subject><subject>Antipsychotic Agents - therapeutic use</subject><subject>Benzodiazepines - adverse effects</subject><subject>Benzodiazepines - therapeutic use</subject><subject>Biomarkers, Pharmacological</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Children & youth</subject><subject>Drug therapy</subject><subject>Electrocardiography - drug effects</subject><subject>Female</subject><subject>Heart Rate - drug effects</subject><subject>Humans</subject><subject>Long QT Syndrome - chemically induced</subject><subject>Long QT Syndrome - diagnosis</subject><subject>Longitudinal Studies</subject><subject>Male</subject><subject>Pediatrics</subject><subject>Prospective Studies</subject><subject>Quetiapine Fumarate - adverse effects</subject><subject>Quetiapine Fumarate - therapeutic use</subject><subject>Risperidone - adverse effects</subject><subject>Risperidone - therapeutic use</subject><subject>Studies</subject><issn>1044-5463</issn><issn>1557-8992</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqF0c1rHCEYwGEpDU2a5phrEXrpZbZ-jDr2NixNG0gJSTfnwdF3shNmdaNOYPvXx81HD7n0IAo-vCg_hE4pWVDS6G_WbBeMULEoi75DR1QIVTVas_flTOq6ErXkh-hjSneEUC6J_IAOmVRKaymP0N-2T-At4DDg5dr4W8Cjx8sQI9gMDl-t8LnPEB_M9HSxHicXwWPjHW5dmCBZ8Dnha7AwPoz-Frc-j9u0s-uQR4tXEUzeFPIdt5gy_Dv4vMZ_8ux2n9DBYKYEJy_7Mbo5-7Fa_qouLn-eL9uLynJR58oRwglTlAmQPTFSUsO5o9KBGwRhVvacSisdU5KDVcOg3KAFZQ3rOSGD4cfo6_PcbQz3M6Tcbcby6mkyHsKcOtoIXTei1ur_VGnVyIbIPf3yht6FOfrykScldOnBiqqelY0hpQhDt43jxsRdR0m379eVft2-X7fvV_znl6lzvwH3T78G449tlpRb</recordid><startdate>201606</startdate><enddate>201606</enddate><creator>Alda, José A</creator><creator>Muñoz-Samons, Daniel</creator><creator>Tor, Jordina</creator><creator>Merchán-Naranjo, Jessica</creator><creator>Tapia-Casellas, Cecilia</creator><creator>Baeza, Inmaculada</creator><creator>Calvo-Escalona, Rosa</creator><creator>Castro-Fornieles, Josefina</creator><creator>Martínez-Cantarero, Carmen</creator><creator>Andrés-Nestares, Patricia</creator><creator>Fernández-Avilés, Francisco</creator><creator>Arango, Celso</creator><general>Mary Ann Liebert, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QG</scope><scope>7RV</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>201606</creationdate><title>Absence of Change in Corrected QT Interval in Children and Adolescents Receiving Antipsychotic Treatment: A 12 Month Study</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c354t-d003027125e6b0a661a33d16dedf502c6b316c6d2763ec7ff7df951282b300fa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adolescent</topic><topic>Antipsychotic Agents - adverse effects</topic><topic>Antipsychotic Agents - therapeutic use</topic><topic>Benzodiazepines - adverse effects</topic><topic>Benzodiazepines - therapeutic use</topic><topic>Biomarkers, Pharmacological</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Children & youth</topic><topic>Drug therapy</topic><topic>Electrocardiography - drug effects</topic><topic>Female</topic><topic>Heart Rate - drug effects</topic><topic>Humans</topic><topic>Long QT Syndrome - chemically induced</topic><topic>Long QT Syndrome - diagnosis</topic><topic>Longitudinal Studies</topic><topic>Male</topic><topic>Pediatrics</topic><topic>Prospective Studies</topic><topic>Quetiapine Fumarate - adverse effects</topic><topic>Quetiapine Fumarate - therapeutic use</topic><topic>Risperidone - adverse effects</topic><topic>Risperidone - therapeutic use</topic><topic>Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Alda, José A</creatorcontrib><creatorcontrib>Muñoz-Samons, Daniel</creatorcontrib><creatorcontrib>Tor, Jordina</creatorcontrib><creatorcontrib>Merchán-Naranjo, Jessica</creatorcontrib><creatorcontrib>Tapia-Casellas, Cecilia</creatorcontrib><creatorcontrib>Baeza, Inmaculada</creatorcontrib><creatorcontrib>Calvo-Escalona, Rosa</creatorcontrib><creatorcontrib>Castro-Fornieles, Josefina</creatorcontrib><creatorcontrib>Martínez-Cantarero, Carmen</creatorcontrib><creatorcontrib>Andrés-Nestares, Patricia</creatorcontrib><creatorcontrib>Fernández-Avilés, Francisco</creatorcontrib><creatorcontrib>Arango, Celso</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Psychology</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of child and adolescent psychopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Alda, José A</au><au>Muñoz-Samons, Daniel</au><au>Tor, Jordina</au><au>Merchán-Naranjo, Jessica</au><au>Tapia-Casellas, Cecilia</au><au>Baeza, Inmaculada</au><au>Calvo-Escalona, Rosa</au><au>Castro-Fornieles, Josefina</au><au>Martínez-Cantarero, Carmen</au><au>Andrés-Nestares, Patricia</au><au>Fernández-Avilés, Francisco</au><au>Arango, Celso</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Absence of Change in Corrected QT Interval in Children and Adolescents Receiving Antipsychotic Treatment: A 12 Month Study</atitle><jtitle>Journal of child and adolescent psychopharmacology</jtitle><addtitle>J Child Adolesc Psychopharmacol</addtitle><date>2016-06</date><risdate>2016</risdate><volume>26</volume><issue>5</issue><spage>449</spage><epage>457</epage><pages>449-457</pages><issn>1044-5463</issn><eissn>1557-8992</eissn><abstract>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.</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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