Tsujii Noa, Okada Takashi, Usami Masahide, Kuwabara Hidenori, Fujita Junichi, Negoro Hideki, Iida Junzo, Aoki Yumi, Takaesu Yoshikazu, Saito Takuya
Department of Child Mental Health and Development Toyama University Hospital Toyama Toyama Japan.
Department of Neuropsychiatry Kindai University Faculty of Medicine Osakasayama Osaka Japan.
PCN Rep. 2022 Nov 14;1(4):e57. doi: 10.1002/pcn5.57. eCollection 2022 Dec.
Current clinical guidelines for attention-deficit/hyperactivity disorder (ADHD) put shared decision making (SDM) at the center of care. However, there remain challenges in SDM in ADHD management, particularly regarding the decision to continue or discontinue medication after ADHD remission in adult patients. We aimed to develop a decision aid (DA) for adult patients with ADHD regarding the continuation or discontinuation of their ongoing ADHD medications after they have attained remission.
We systematically developed a DA according to the International Patient Decision Aid Standard (IPDAS). First, we created a DA prototype using the results of our previous systematic review and meta-analysis that identified the consequences of continuing and discontinuing ADHD medications. Second, we administered a mixed-method questionnaire (alpha acceptability testing) to adult patients with ADHD and healthcare providers to improve the DA prototype and develop it into a final version that is acceptable for clinical settings.
Our DA consisted of ADHD description, the option to continue or discontinue ADHD medications, the advantages and disadvantages of the consequences, as well as value clarification exercises for each option. Patients ( = 20) reported that the DA had acceptable language (85%), adequate information (75%), and a well-balanced presentation (53%). Healthcare providers ( = 19) provided favorable feedback. The final DA met all six IPDAS requisite criteria.
Our results could facilitate the SDM process between patients and healthcare providers on the continuation or discontinuation of ADHD medication following remission. Further studies should verify the effects of using the DA during the SDM process among patients across the age spectrum with ADHD and healthcare providers.
当前注意力缺陷多动障碍(ADHD)临床指南将共同决策(SDM)置于治疗核心。然而,ADHD管理中的共同决策仍存在挑战,尤其是在成年患者ADHD缓解后决定继续或停用药物方面。我们旨在为成年ADHD患者开发一种决策辅助工具(DA),用于在病情缓解后决定是否继续使用当前的ADHD药物。
我们根据国际患者决策辅助标准(IPDAS)系统地开发了一种决策辅助工具。首先,我们利用之前的系统评价和荟萃分析结果创建了一个决策辅助工具原型,该分析确定了继续和停用ADHD药物的后果。其次,我们对成年ADHD患者和医疗服务提供者进行了一项混合方法问卷调查(α可接受性测试),以改进决策辅助工具原型,并将其开发成临床环境可接受的最终版本。
我们的决策辅助工具包括ADHD描述、继续或停用ADHD药物的选项、后果的优缺点,以及每个选项的价值观澄清练习。患者(n = 20)报告说,决策辅助工具的语言可接受(85%)、信息充分(75%)且呈现平衡(53%)。医疗服务提供者(n = 19)提供了积极反馈。最终的决策辅助工具符合所有六项IPDAS必要标准。
我们的结果可能有助于患者和医疗服务提供者就缓解后ADHD药物的继续或停用进行共同决策。进一步的研究应验证在不同年龄段的ADHD患者和医疗服务提供者的共同决策过程中使用该决策辅助工具的效果。