Skriptshak Courtney, Reich Ashley
Mental Health Clinical Pharmacy Specialist, North Florida/South Georgia Veterans Health System, Lake City, Florida.
Ment Health Clin. 2021 Jul 16;11(4):259-262. doi: 10.9740/mhc.2021.07.259. eCollection 2021 Jul.
Over the past few years, intranasal esketamine has been FDA-approved for treatment-resistant depression as well as MDD with suicidal ideation. In the clinical trials leading to the recent FDA approvals, subjects with a diagnosis of bipolar disorder were excluded from participation in the trial. The manufacturer of intranasal esketamine states that it "has not been studied, and is not indicated, for patients with bipolar disorder." Antidepressants are commonly associated with having the potential to induce rapid cycling in patients with bipolar disorder, though the mechanism is not fully understood. This case report demonstrates the potential safety of intranasal esketamine in combination with mood stabilizer therapy in a patient diagnosed with bipolar disorder without recent history of manic or hypomanic episodes.
在过去几年中,鼻内用艾司氯胺酮已获美国食品药品监督管理局(FDA)批准用于治疗抵抗性抑郁症以及伴有自杀观念的重度抑郁症(MDD)。在导致近期FDA批准的临床试验中,被诊断为双相情感障碍的受试者被排除在试验参与之外。鼻内用艾司氯胺酮的制造商表示,“尚未对双相情感障碍患者进行研究,也未表明适用于该类患者”。抗抑郁药通常被认为有可能诱发双相情感障碍患者的快速循环发作,尽管其机制尚未完全明确。本病例报告展示了鼻内用艾司氯胺酮与心境稳定剂联合治疗在一名被诊断为双相情感障碍且近期无躁狂或轻躁狂发作史患者中的潜在安全性。