Clarity and applicability of adverse drug reaction-related monitoring instructions in clinical practice guidelines for children and adolescents treated with antipsychotic drugs: a review of six clinical practice guidelines

被引:2
|
作者
Minjon, Lenneke [1 ]
Aarts, Juul W. [1 ]
van den Ban, Els [2 ]
Egberts, Toine C. G. [1 ,3 ]
Heerdink, Eibert R. [1 ,4 ]
机构
[1] Univ Utrecht, Fac Sci, Utrecht Inst Pharmaceut Sci, Div Pharmacoepidemiol & Clin Pharmacol, Utrecht, Netherlands
[2] Altrecht, Dept Child & Adolescent Psychiat, Utrecht, Netherlands
[3] Univ Med Ctr Utrecht, Dept Clin Pharm, Utrecht, Netherlands
[4] HU Univ Appl Sci Utrecht, Res Grp Innovat Pharmaceut Care, Utrecht, Netherlands
来源
BMJ OPEN | 2022年 / 12卷 / 03期
关键词
child & adolescent psychiatry; adverse events; protocols & guidelines; 2ND-GENERATION ANTIPSYCHOTICS; RECOMMENDATIONS; QUALITY;
D O I
10.1136/bmjopen-2021-058940
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives Monitoring instructions related to adverse drug reactions (ADRs) are not always clearly described in clinical practice guidelines (CPGs) and not always easily applicable in daily clinical practice. The aim of this study was to assess the clarity of presentation and the applicability of ADR-related monitoring instructions in CPGs for children and adolescents treated with antipsychotic drugs. Setting Guidelines from different countries were selected, and monitoring instructions for 13 ADR-related parameters were assessed. Primary and secondary outcome measures To assess the clarity and the applicability of the sections concerning monitoring instructions in each CPG, the Appraisal of Guidelines for Research and Evaluation instrument was used. To assess the clarity and the applicability of the monitoring instructions for each ADR-related parameter, the Systematic Information for Monitoring score was used. Results Six CPGs were included. Overall, the presentation of the monitoring instructions in the different CPGs was clear; three CPGs scored >75%. All CPGs scored lower on applicability, as, for example, the barriers and facilitators were poorly described. The number of ADR-related parameters included in the CPGs varied between 8 and 13. Why and what to monitor was always described for each parameter. When to start monitoring was also often described (90.2%), but when to stop monitoring was less frequently described (37.4%). Conclusions The CPGs differed on the parameters that needed to be monitored. Overall, the monitoring instructions were clearly presented, but improvement in their applicability is required. By improving the monitoring instructions, CPGs can provide better guidance on monitoring ADRs in daily clinical practice.
引用
收藏
页数:9
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