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Open AccessJournal ArticleDOI

Management of Adverse Effects of Second-generation Antipsychotics in Youth

TLDR
Short-term and long-term adverse effects of SGAs in youth populations are exposed and management recommendations for major adverse effects are provided to aid clinicians in making treatment decisions.
Abstract
Second-generation antipsychotics (SGAs) have been proven effective in treating several psychiatric conditions in children and adolescents. These atypical antipsychotic medications are being used with increasing frequency in Europe, the U.S., and Canada. We aim to expose short-term and long-term adverse effects (AEs) of SGAs in youth populations and to provide management recommendations for major adverse effects. These proposals are based on (1) an in-depth literature review of both short- and long-term studies on the use of SGAs in youth; (2) our own clinical experience in managing such treatment in this population; and (3) the work of the Canadian Alliance for Monitoring Effectiveness and Safety of Antipsychotics in Children (CAMESA). AEs are frequent in youth treated with SGAs, and include primarily weight gain, metabolic and hormonal changes, somnolence, extrapyramidal syndrome, and QT modifications. However, frequency and type of AE vary according to compound, and each compound’s AE profile is specific. Acknowledgment of these distinct profiles should aid clinicians in making treatment decisions. After an SGA is prescribed, routine monitoring of AEs is recommended, and should an AE occur, clinical management recommendations should be followed. To date, there are no clinically validated monitoring recommendations.

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Preliminary and ongoing French multicenter prospective naturalistic study of adverse events of antipsychotic treatment in naive children and adolescents

TL;DR: All adolescents experienced AE, with significant weight gain being observed in all patients who completed the 12-week follow-up, and further evidence for the necessity of national safety guidelines for AP prescription in the pediatric population is provided.
Journal ArticleDOI

Pediatric Antipsychotic Use and Outcomes Monitoring.

TL;DR: An example of the use of the HealthTracker in the CIPPRD is provided to demonstrate how it can be used for ATP-related outcome monitoring in complex neurodisability within routine clinical practice.
Journal ArticleDOI

Incidence of adverse events in antipsychotic-naïve children and adolescents treated with antipsychotic drugs: a French multicentre naturalistic study protocol (ETAPE)

TL;DR: This study will enable better characterisation of the prescription of AP drugs in an AP-naïve paediatric population named Etude de la Tolérance des AntiPsychotique chez l'Enfant (ETAPE), and help to develop quality standards and recommendations for monitoring AE during the prescriptions of AP.
References
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Bipolar Disorder

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Consensus Development Conference on Antipsychotic Drugs and Obesity and Diabetes Response to consensus statement

TL;DR: The ADA concluded that aripiprazole and ziprasidone have no effect on the risk of diabetes, solely based on data from clinical trials that did not include these two drugs in epidemiological studies.
Journal ArticleDOI

Randomized Controlled Trial of the Effect on Quality of Life of Second- vs First-Generation Antipsychotic Drugs in Schizophrenia: Cost Utility of the Latest Antipsychotic Drugs in Schizophrenia Study (CUtLASS 1)

TL;DR: In people with schizophrenia whose medication is changed for clinical reasons, there is no disadvantage across 1 year in terms of quality of life, symptoms, or associated costs of care in using FGAs rather than nonclozapine SGAs.
Journal ArticleDOI

Cardiometabolic risk of second-generation antipsychotic medications during first-time use in children and adolescents.

TL;DR: Weight gain and changes in lipid and metabolic parameters in patients without prior antipsychotic medication exposure are studied and mean levels increased significantly for total cholesterol, triglycerides, and non-high-density lipoprotein cholesterol.
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