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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mary Ann Liebert, Inc., publishers
2021
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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. |
format | Online Article Text |
id | pubmed-7891197 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Mary Ann Liebert, Inc., publishers |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT karaimaan impactofantipsychoticguidelinesonlaboratorymonitoringinchildrenwithneurodevelopmentaldisorders AT pennermelanie impactofantipsychoticguidelinesonlaboratorymonitoringinchildrenwithneurodevelopmentaldisorders |