水疱单胺转运2抑制剂的临床经验及治疗考虑。

The mental health clinician Pub Date : 2024-12-02 eCollection Date: 2024-12-01 DOI:10.9740/mhc.2024.12.304
Kayla Johnson
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引用次数: 0

摘要

水疱单胺转运蛋白2抑制剂(VMAT2i)目前已被美国食品和药物管理局批准用于治疗亨廷顿舞蹈病和迟发性运动障碍。此外,在临床实践中,它们经常用于其他多动运动障碍。由于缺乏面对面的临床试验,临床环境中VMAT2i的管理可能不明确,并依赖于从业者的临床经验。由于有限的分销模式,通常要求VMAT2i由专业药房分配,获取和开始治疗可能存在障碍。患者病例允许探索VMAT2i之间的切换,替代给药途径,在儿科和非标签条件下的使用,以及如何成功启动和监测VMAT2i治疗的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical experience and treatment considerations with vesicular monoamine transport 2 inhibitors.

Vesicular monoamine transporter 2 inhibitors (VMAT2i) are currently Food and Drug Administration-approved for the treatment of Huntington disease chorea and tardive dyskinesia. Additionally, they are often used for other hyperkinetic movement disorders in clinical practice. Due to a lack of head-to-head clinical trials, management of VMAT2i in the clinical setting may be unclear and rely on the clinical experience of the practitioner. Due to the limited distribution model, which typically requires VMAT2i to be dispensed by specialty pharmacies, access and initiation of treatment may present as barriers. Patient cases allow for the exploration of switching between VMAT2i, alternative routes of administration, utilization in pediatric and off-label conditions, and how to successfully initiate and monitor a patient on VMAT2i therapy.

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