
Safety Monitoring and Treatment Continuation With Esketamine in TRD
The expert psychiatrist examined safety as a layered process that begins with a trusting therapeutic relationship, continues with screening for medical contraindications and coordination with other clinicians, and extends to set, setting, and on-site emergency equipment.
Episodes in this series

In this episode, ‘Safety Monitoring and Treatment Continuation With Esketamine in TRD,’ the expert psychiatrist explores the following questions:
What does day-to-day safety monitoring for esketamine look like in treatment-resistant depression, and what are common misconceptions about the protocol?
What data support continuing esketamine therapy in treatment-resistant depression, and what most often leads patients to stop?
The expert psychiatrist examined safety as a layered process that begins with a trusting therapeutic relationship, continues with screening for medical contraindications and coordination with other clinicians, and extends to set, setting, and on-site emergency equipment. He clarified that vital signs every 5 minutes are not mandated and that monitoring should fit both the patient and the medication’s profile. Citing the SUSTAIN trials, he noted that responders who discontinue relapse after about a month on average, and listed insurance changes, moves, a wish to pause, intolerability, and inadequate response as common reasons for stopping.
Throughout the conversation, the experts provide a comprehensive reflection on the field and the factors that may shape how clinicians approach care moving forward.
The next episode in this series, ‘Building an Interventional TRD Practice: From Setup to the Patient Experience,’ features the panelists advancing their conversation on treatment-resistant depression and focusing on how they launched their practice and what treatment asks of patients.
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