Correll Christoph U, Mafi Charlotte Emborg, Fagiolini Andrea, Seerden Paul, Seifritz Erich, Tiihonen Jari, Vita Antonio, Citrome Leslie
Zucker Hillside Hospital, Department of Psychiatry, Northwell Health, Glen Oaks, New York, USA.
Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Department of Psychiatry and Molecular Medicine, Hempstead, New York, USA.
Neuropsychiatr Dis Treat. 2025 Aug 29;21:1857-1883. doi: 10.2147/NDT.S539306. eCollection 2025.
Brexpiprazole is a second-generation antipsychotic with multiple indications, including the treatment of schizophrenia. As a partial dopamine agonist, brexpiprazole differs from most other antipsychotics, yet uncertainties about its full mechanism of action have led to some ambiguity among prescribers. To address this gap, an international panel of psychiatric experts was organized and convened with funding from Otsuka Pharmaceutical Europe Ltd and H. Lundbeck A/S to discuss the safe and effective use of brexpiprazole across different stages of schizophrenia treatment. Brexpiprazole's pharmacological profile-characterized by balanced binding affinities across norepinephrine, dopamine, and serotonin receptors-contributes to its efficacy in multiple symptom domains, including agitation and negative symptoms. Its tolerable safety profile, marked by minimal activation and minimal sedation and a relatively low risk of long-term cardiometabolic concerns, further supports its clinical utility. Brexpiprazole is a viable first-line therapy in both inpatient and outpatient settings when properly titrated and monitored. Brexpiprazole also serves as an option for different symptom domains in schizophrenia and for patients needing to switch antipsychotics due to inadequate symptom control or intolerable adverse events. Long-term maintenance therapy is essential for relapse prevention in schizophrenia, and when prescribed at appropriate doses for psychotic symptom control, brexpiprazole can provide sustained benefits with minimal long-term safety concerns. This report outlines the consensus panel's recommendations on the optimal initiation and administration of brexpiprazole in management of schizophrenia treatment, including a treatment algorithm, which is supported by a literature review.
布雷哌唑是一种具有多种适应症的第二代抗精神病药物,包括用于治疗精神分裂症。作为一种部分多巴胺激动剂,布雷哌唑与大多数其他抗精神病药物不同,然而其完整作用机制的不确定性导致处方医生之间存在一些困惑。为了填补这一空白,在大冢制药欧洲有限公司和H. 伦贝克公司的资助下,组织并召集了一个国际精神科专家小组,讨论布雷哌唑在精神分裂症治疗不同阶段的安全有效使用。布雷哌唑的药理学特性——其特点是对去甲肾上腺素、多巴胺和5-羟色胺受体具有平衡的结合亲和力——有助于其在多个症状领域发挥疗效,包括激越和阴性症状。其可耐受的安全性特征,表现为最小的激活作用、最小的镇静作用以及长期心脏代谢问题风险相对较低,进一步支持了其临床实用性。在进行适当的滴定和监测时,布雷哌唑在住院和门诊环境中都是一种可行的一线治疗药物。布雷哌唑也是精神分裂症不同症状领域以及因症状控制不佳或出现无法耐受的不良事件而需要更换抗精神病药物的患者的一种选择。长期维持治疗对于预防精神分裂症复发至关重要,当以适当剂量处方用于控制精神病性症状时,布雷哌唑可以提供持续的益处,且长期安全性问题最小。本报告概述了共识小组关于布雷哌唑在精神分裂症治疗管理中的最佳起始和给药方法的建议,包括一种治疗算法,该算法得到了文献综述的支持。