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THE IMPACT OF INTRANASAL ESKETAMINE ON TREATMENT-RESISTANT DEPRESSION: A SYSTEMATIC REVIEW

Wojciech Kotlarski, Klaudia Magdalena Kotlarska, Tomasz Stanisław Mainka, Emil Sergejuk

International Journal of Innovative Technologies in Social Science June 25, 2026 DOI: 10.31435/ijitss.2(50).2026.5523 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Systematic review Randomized Qualitative Peer reviewed
Population Adults with treatment-resistant depression
Intervention Intranasal esketamine
Topics Depression Ketamine Esketamine
Keywords Adverse effect Nasal administration Systematic review Randomized controlled trial Depression economics Clinical trial Meta-analysis Nausea Medline Tolerability Anesthesia
Key findings Intranasal esketamine is associated with greater symptom improvement and higher response rates than control in TRD, but with more frequent adverse events such as dizziness and nausea.

Abstract

Introduction: Treatment-resistant depression (TRD) is a major public health and societal challenge, associated with persistent symptoms, functional impairment, and increased healthcare and economic burden. Intranasal esketamine has emerged as a rapid-acting adjunctive therapy with a distinct glutamatergic mechanism of action. This systematic review summarizes current evidence on its effectiveness and implementation-relevant outcomes in TRD.

Methods: A systematic literature review was conducted in accordance with PRISMA 2020. PubMed/MEDLINE and EMBASE were searched for English-language systematic reviews and meta-analyses published between 2010 and 2026 using database-specific but equivalent Boolean strategies combining intranasal esketamine terms with TRD terms. Titles/abstracts were screened and eligible records underwent full-text assessment. Five studies were included in qualitative synthesis. The last search was conducted on 5 March 2026.

Results: Meta-analytic evidence from randomized trials reported greater symptom improvement with intranasal esketamine versus control (MADRS SMD = −3.88; 95% CI −5.71 to −2.05) and higher response rates (RR = 1.99; 95% CI 1.28–3.10), alongside improvements in disability (SDS SMD = −3.01) and patient-reported symptoms (PHQ-9 SMD = −2.32). Adverse events were more frequent, including dizziness (RR = 3.55) and nausea (RR = 3.88). Real-world data showed substantial symptom reduction (Hedges’ g = −1.98) and higher remission likelihood at three months (OR = 5.1), with high overall adverse-event prevalence (82%) and dissociation commonly reported (49%).

Conclusions: Intranasal esketamine shows clinically relevant benefits in TRD with convergent trial and real-world signals, but requires supervised delivery and sustained follow-up. Further research should clarify long-term outcomes, clinical meaningfulness, and health-system cost-effectiveness.

Comparable studies

Other systematic reviews and meta-analyses on esketamine for depression, most cited first.

Study Year Design Participants
Comparative efficacy of racemic ketamine and esketamine for depression: a systematic review and meta-analysis Adults with unipolar or bipolar major depression 2020 Systematic review and meta-analysis n = 1,877
The acute antisuicidal effects of single-dose intravenous ketamine and intranasal esketamine in individuals with major depression and bipolar disorders: A systematic review and meta-analysis. Participants in randomized controlled trials of ketamine for suicidal ideation 2020 Systematic review and meta-analysis n = 197
Efficacy of Esketamine Augmentation in Major Depressive Disorder Patients with major depressive disorder who are treatment-resistant or acutely suicidal 2020 Systematic review and meta-analysis n = 774
Esketamine Treatment for Depression in Adults: A PRISMA Systematic Review and Meta-Analysis. Patients with treatment-resistant major depressive disorder 2025 Systematic review and meta-analysis
EFFICACY AND SAFETY OF RACEMIC KETAMINE AND ESKETAMINE FOR DEPRESSION: A SYSTEMATIC REVIEW AND META-ANALYSIS Adults with unipolar or bipolar major depression 2022 Systematic review and meta-analysis n = 2,903

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