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

被引:7
|
作者
Kara, Imaan [1 ]
Penner, Melanie [2 ,3 ]
机构
[1] Univ Toronto, Fac Med, Toronto, ON, Canada
[2] Holland Bloorview Kids Rehabil Hosp, Bloorview Res Inst, Autism Res Ctr, 150 Kilgour Rd, Toronto, ON M4G 1R8, Canada
[3] Univ Toronto, Dept Paediat, Toronto, ON, Canada
关键词
child development disorders; autism spectrum disorders; autism; antipsychotics; psychotropic drugs; RECOMMENDATIONS; IRRITABILITY; ARIPIPRAZOLE; ADOLESCENTS; SAFETY; TRENDS; YOUTH;
D O I
10.1089/cap.2020.0096
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
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.
引用
收藏
页码:79 / 83
页数:5
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