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Impact of Antipsychotic Guidelines on Laboratory Monitoring in Children with Neurodevelopmental Disorders

Objectives: The Canadian Alliance for Monitoring Effectiveness and Safety of Antipsychotics in Children (CAMESA) guidelines provide monitoring recommendations for children who are treated with second-generation antipsychotics (SGAs). The objective of this study was to determine the impact of the CAM...

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Autores principales: Kara, Imaan, Penner, Melanie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc., publishers 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7891197/
https://www.ncbi.nlm.nih.gov/pubmed/33052712
http://dx.doi.org/10.1089/cap.2020.0096
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author Kara, Imaan
Penner, Melanie
author_facet Kara, Imaan
Penner, Melanie
author_sort Kara, Imaan
collection PubMed
description Objectives: The Canadian Alliance for Monitoring Effectiveness and Safety of Antipsychotics in Children (CAMESA) guidelines provide monitoring recommendations for children who are treated with second-generation antipsychotics (SGAs). The objective of this study was to determine the impact of the CAMESA guidelines on SGA monitoring in children with neurodevelopmental disorders. Methods: A retrospective chart review compared laboratory monitoring in children treated with SGAs who were referred to a tertiary psychopharmacology clinic before (2008–2011) and after (2013–2016) CAMESA publication. Chi-squared tests were used to detect changes in SGA use and monitoring between the two time periods. Results: A total of 345 charts were reviewed (n = 136 pre-CAMESA, n = 209 post-CAMESA). The proportion of children taking an SGA increased significantly (35% vs. 49%; p = 0.02) as did the duration of SGA treatment before tertiary assessment (18.6 months vs. 27.2 months; p = 0.03). SGA monitoring data were missing in 40% of charts pre-CAMESA and in 31% of charts post-CAMESA. The proportion of patients with any available laboratory monitoring did not change between the time periods (35% pre-CAMESA vs. 39% post-CAMESA; p = 0.56). Similarly, the proportion of patients with full laboratory monitoring was not significantly different between time periods (15% pre-CAMESA vs. 25% post-CAMESA; p = 0.23). Conclusions: SGA monitoring rates did not significantly improve after CAMESA guideline publication. To maximize benefit and mitigate risks of these medications, there is a need to identify barriers to SGA monitoring.
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spelling pubmed-78911972021-02-19 Impact of Antipsychotic Guidelines on Laboratory Monitoring in Children with Neurodevelopmental Disorders Kara, Imaan Penner, Melanie J Child Adolesc Psychopharmacol Brief Report Objectives: The Canadian Alliance for Monitoring Effectiveness and Safety of Antipsychotics in Children (CAMESA) guidelines provide monitoring recommendations for children who are treated with second-generation antipsychotics (SGAs). The objective of this study was to determine the impact of the CAMESA guidelines on SGA monitoring in children with neurodevelopmental disorders. Methods: A retrospective chart review compared laboratory monitoring in children treated with SGAs who were referred to a tertiary psychopharmacology clinic before (2008–2011) and after (2013–2016) CAMESA publication. Chi-squared tests were used to detect changes in SGA use and monitoring between the two time periods. Results: A total of 345 charts were reviewed (n = 136 pre-CAMESA, n = 209 post-CAMESA). The proportion of children taking an SGA increased significantly (35% vs. 49%; p = 0.02) as did the duration of SGA treatment before tertiary assessment (18.6 months vs. 27.2 months; p = 0.03). SGA monitoring data were missing in 40% of charts pre-CAMESA and in 31% of charts post-CAMESA. The proportion of patients with any available laboratory monitoring did not change between the time periods (35% pre-CAMESA vs. 39% post-CAMESA; p = 0.56). Similarly, the proportion of patients with full laboratory monitoring was not significantly different between time periods (15% pre-CAMESA vs. 25% post-CAMESA; p = 0.23). Conclusions: SGA monitoring rates did not significantly improve after CAMESA guideline publication. To maximize benefit and mitigate risks of these medications, there is a need to identify barriers to SGA monitoring. Mary Ann Liebert, Inc., publishers 2021-02-01 2021-02-11 /pmc/articles/PMC7891197/ /pubmed/33052712 http://dx.doi.org/10.1089/cap.2020.0096 Text en © Imaan Kara and Melanie Penner 2021; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons Attribution Noncommercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are cited.
spellingShingle Brief Report
Kara, Imaan
Penner, Melanie
Impact of Antipsychotic Guidelines on Laboratory Monitoring in Children with Neurodevelopmental Disorders
title Impact of Antipsychotic Guidelines on Laboratory Monitoring in Children with Neurodevelopmental Disorders
title_full Impact of Antipsychotic Guidelines on Laboratory Monitoring in Children with Neurodevelopmental Disorders
title_fullStr Impact of Antipsychotic Guidelines on Laboratory Monitoring in Children with Neurodevelopmental Disorders
title_full_unstemmed Impact of Antipsychotic Guidelines on Laboratory Monitoring in Children with Neurodevelopmental Disorders
title_short Impact of Antipsychotic Guidelines on Laboratory Monitoring in Children with Neurodevelopmental Disorders
title_sort impact of antipsychotic guidelines on laboratory monitoring in children with neurodevelopmental disorders
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7891197/
https://www.ncbi.nlm.nih.gov/pubmed/33052712
http://dx.doi.org/10.1089/cap.2020.0096
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