Efficacy of Intranasal Esketamine in Treatment-Resistant Depression: A Six-Month Real-World Follow-Up Study of Depressive Symptoms, Hopelessness, and Suicide Risk.
Maurizio Pompili, Maria Anna Trocchia, Ludovica Longhini, Eva Dispenza, Cristina Di Legge, Salvatore Sarubbi, Denise Erbuto, Isabella Berardelli
Human psychopharmacology July 1, 2025 DOI: 10.1002/hup.70008 via PubMed
Summary
AI-generated from the abstractIn a real-world outpatient setting, 21 patients with treatment-resistant depression received intranasal esketamine. Depressive symptoms, measured by clinician and self-report scales, decreased at 3-month and 6-month follow-ups. Suicidal ideation significantly declined between baseline and 6 months, and patients also reported reduced hopelessness over time. The findings suggest intranasal esketamine is associated with improvements in depressive symptoms, hopelessness, and suicidal ideation in treatment-resistant depression.
Study at a glance
| Characteristics | Observational cohort Peer reviewed |
|---|---|
| Sample size | 21 |
| Population | Patients diagnosed with treatment-resistant depression |
| Intervention | Intranasal esketamine |
| Duration | 6-month follow-up |
| Topics | Depression Esketamine |
| Keywords | Suicide prevention Suicide risk Treatment‐resistant depression |
| Citations | 3 |
| Key finding | Intranasal esketamine was associated with decreased depressive symptoms, reduced suicidal ideation, and lower hopelessness at 3-month and 6-month follow-ups in treatment-resistant depression. |
Abstract
Treatment-resistant depression is one of the most significant clinical challenges in psychiatric practice. The primary aim of the present study was to assess the efficacy and tolerability of intranasal esketamine on depressive symptoms in a real-world outpatient setting. A secondary objective was to explore the potential benefits of intranasal esketamine on hopelessness and suicide risk (suicidal ideation and suicide attempts). Twenty-one patients diagnosed with treatment-resistant depression were treated with intranasal esketamine. Depressive symptoms (MADRS and BDI), suicide risk (C-SSRS), and hopelessness (BHS) were assessed. We conducted a mixed model for repeated measures analysis to evaluate changes from baseline (T0), 3-month follow-up (T1), and 6-month follow-up (T2). Results indicated that depressive symptoms decreased over time. Specifically, both clinician and self-report measures show lower levels of depressive symptoms at 3-month and 6-month follow-up. We also found a significant decrease in the presence of suicidal ideation between T0 and T2. Finally, patients also reported a reduction in hopelessness levels over time. Our findings indicate an overall response regarding depressive symptoms, hopelessness, and suicidal ideation after esketamine in treatment-resistant depression at 3-month and 6-month follow-up assessments.