Sulaiman Ahmad Hatim, Amin Mustafa M, Ang Jin Kiat, Ho Roger, Nik Jaafar Nik Ruzyanei, Ng Chong Guan, Wibowo Nurhidayat Adhi, Paholpak Pongsatorn, Pariwatcharakul Pornjira, Sanguanvichaikul Thitima, Ung Eng Khean, Wardani Natalia Dewi, Yeo Brian
Department of Psychological Medicine, Faculty of Medicine, Universiti Malaya, Kuala Lumpur 50603, Malaysia.
Department of Psychiatry, Faculty of Medicine, Universitas Sumatera Utara, Medan 20222, Indonesia.
Healthcare (Basel). 2025 May 30;13(11):1304. doi: 10.3390/healthcare13111304.
: Cariprazine, a D3/D2 partial agonist, is one of the few recommended treatment options for bipolar 1 disorder (BP1D) in Southeast Asia. This study aims to generate insights from leading experts on the safe and effective use of cariprazine for BP1D, specifically by formulating practical recommendations not thoroughly covered in the existing literature. : A formal consensus methodology using the modified RAND/UCLA Appropriateness Method was employed to develop consensus recommendations. The methodology included a targeted literature search, creation of clinical scenarios, two rounds of rating of the appropriateness of each scenario on a nine-point Likert scale by an expert panel of psychiatrists from Southeast Asia ( = 13), and a face-to-face discussion among the expert panel between the two rounds of rating. In the absence of disagreement, scenarios were classified as appropriate (7-9), equivocal (4-6), or inappropriate (1-3) based on median scores. Clinical scenarios were subsequently converted to consensus recommendations upon approval by the expert panel. : Most experts recommended a 4-8-week trial of cariprazine for bipolar depression (85%) and 3-4 weeks for acute mania/mixed (71%). For longer treatment, 61.5% and 69% recommended >1 year for acute mania/mixed and bipolar depression, respectively. Cariprazine was also considered suitable as first-line therapy, including for first-episode bipolar depression (Mdn: 8, IQR: 7-9) and first-episode mania (Mdn: 8; IQR: 8-9). : The consensus recommendations may serve as practical guidance for clinicians to make informed decisions regarding the management of adult patients with BP1D, while considering the preferences and circumstances of individual patients.
卡立普嗪是一种D3/D2部分激动剂,是东南亚双相I型障碍(BP1D)少数推荐的治疗选择之一。本研究旨在从权威专家处获取关于卡立普嗪安全有效治疗BP1D的见解,特别是通过制定现有文献中未充分涵盖的实用建议。采用改良的兰德/加州大学洛杉矶分校适宜性方法的正式共识方法来制定共识建议。该方法包括有针对性的文献检索、创建临床场景、由来自东南亚的13位精神科医生专家小组在九点李克特量表上对每个场景的适宜性进行两轮评分,以及在两轮评分之间专家小组进行面对面讨论。在无分歧的情况下,根据中位数得分将场景分类为适宜(7 - 9)、模棱两可(4 - 6)或不适宜(1 - 3)。临床场景随后经专家小组批准后转化为共识建议。大多数专家建议对双相抑郁进行4 - 8周的卡立普嗪试验(85%),对急性躁狂/混合发作进行3 - 4周(71%)。对于更长时间的治疗,分别有61.5%和69%的专家建议急性躁狂/混合发作和双相抑郁的治疗时间>1年。卡立普嗪也被认为适合作为一线治疗,包括用于首发双相抑郁(中位数:8,四分位间距:7 - 9)和首发躁狂(中位数:8;四分位间距:8 - 9)。这些共识建议可为临床医生在管理成年BP1D患者时做出明智决策提供实用指导,同时考虑个体患者的偏好和情况。