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Decision aid development and its acceptability among adults with attention-deficit/hyperactivity disorders regarding treatment discontinuation after remission.
Tsujii, Noa; Okada, Takashi; Usami, Masahide; Kuwabara, Hidenori; Fujita, Junichi; Negoro, Hideki; Iida, Junzo; Aoki, Yumi; Takaesu, Yoshikazu; Saito, Takuya.
Afiliação
  • Tsujii N; Department of Child Mental Health and Development Toyama University Hospital Toyama Toyama Japan.
  • Okada T; Department of Neuropsychiatry Kindai University Faculty of Medicine Osakasayama Osaka Japan.
  • Usami M; Department of Developmental Disorders, National Institute of Mental Health National Center of Neurology and Psychiatry Kodaira Tokyo Japan.
  • Kuwabara H; Department of Child and Adolescent Psychiatry, Kohnodai Hospital National Center for Global Health and Medicine Ichikawa Chiba Japan.
  • Fujita J; Senogawa Hospital Hiroshima-shi Hiroshima Japan.
  • Negoro H; Department of Child Psychiatry Yokohama City University Hospital Yokohama Kanagawa Japan.
  • Iida J; Shigisan Hospital Herarland Shigisan Ikoma Nara Japan.
  • Aoki Y; Medical Corporation Nanfukai Manyo Clinic Child Mental Health Care Center Kizuna Kashihara Nara Japan.
  • Takaesu Y; Graduate School of Nursing St. Luke's International University Chuo-ku Tokyo Japan.
  • Saito T; Department of Neuropsychiatry, Graduate School of Medicine University of the Ryukyus Okinawa Japan.
PCN Rep ; 1(4): e57, 2022 Dec.
Article em En | MEDLINE | ID: mdl-38868662
ABSTRACT

Aim:

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.

Method:

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.

Results:

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 (n = 20) reported that the DA had acceptable language (85%), adequate information (75%), and a well-balanced presentation (53%). Healthcare providers (n = 19) provided favorable feedback. The final DA met all six IPDAS requisite criteria.

Conclusions:

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.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article