Warren A E, Hamilton R M, Bélanger S A, Gray C, Gow R M, Sanatani S, Côté J-M, Lougheed J, LeBlanc J, Martin S, Miles B, Mitchell C, Gorman D A, Weiss M, Schachar R
IWK Health Centre, Dalhousie University, Halifax, Nova Scotia.
Can J Cardiol. 2009 Nov;25(11):625-30. doi: 10.1016/s0828-282x(09)70157-6.
Regulatory decisions and scientific statements regarding the management of attention-deficit hyperactivity disorder (ADHD) raise questions about the safety of medications and the appropriate pretreatment evaluation to determine suitability for treatment with medication. This is particularly true in the setting of known structural or functional heart disease. The present paper reviews the available data, including peer-reviewed literature, data from the United States Food and Drug Administration Web site on reported adverse reactions in children using stimulant medication, and Health Canada data on the same problem. A consensus-based guideline on appropriate assessment is provided, based on input from members of the Canadian Paediatric Society, the Canadian Cardiovascular Society and the Canadian Academy of Child and Adolescent Psychiatry, with specific expertise and knowledge in the areas of both ADHD and pediatric cardiology. The present statement advocates a thorough history and physical examination before starting stimulant medications, with an emphasis on the identification of risk factors for sudden death, but does not routinely recommend electrocardiographic screening or cardiac subspecialist consultation unless indicated by history or physical examination findings. A checklist for identifying children who are potentially at risk of sudden death (independent of ADHD or medications used to treat it) is provided. Although recommendations are based on the best evidence currently available, the committee further agrees that more research on this subject is necessary to optimize the approach to this common clinical scenario.
关于注意力缺陷多动障碍(ADHD)管理的监管决策和科学声明引发了有关药物安全性以及确定药物治疗适用性的适当预处理评估的问题。在已知存在结构性或功能性心脏病的情况下尤其如此。本文回顾了现有数据,包括同行评审文献、美国食品药品监督管理局网站上有关使用兴奋剂药物的儿童报告不良反应的数据以及加拿大卫生部关于同一问题的数据。基于加拿大儿科学会、加拿大心血管学会和加拿大儿童与青少年精神病学会成员的意见,提供了一份关于适当评估的基于共识的指南,这些成员在ADHD和儿科心脏病学领域具有特定的专业知识。本声明主张在开始使用兴奋剂药物之前进行全面的病史询问和体格检查,重点是识别猝死的危险因素,但除非病史或体格检查结果表明有必要,否则不常规推荐进行心电图筛查或心脏专科会诊。提供了一份识别可能有猝死风险儿童(与ADHD或用于治疗它的药物无关)的清单。尽管这些建议基于目前可得的最佳证据,但委员会进一步一致认为,有必要对该主题进行更多研究,以优化针对这一常见临床情况的处理方法。