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Clinical guidance on the use of esketamine nasal spray for patients with treatment resistant depression: A European Delphi consensus report

delete2026-07-17
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OA
AI
A
Allan H. Young *
B
Bernhard T. Baune
B
Beatrice Benatti
D
Djamila Bennabi
S
Sven Estercam
P
Philip Gorwood
L
Luís Gutiérrez-Rojas
V
Vassilis Martiadis
P
Patricio Molero
C
Claus Normann
R
Richard Perry
W
William Pitchot
A
Andreas Reif
G
Gianluca Rosso
E
Eduard Vieta
A
Andrea Fagiolini
DOI:10.1016/j.euroneuro.2026.112907delete
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Abstract

Abstract

En 中文
Esketamine nasal spray (NS) is an established treatment for patients with treatment resistant depression (TRD). To further optimise real-world outcomes, consensus is needed regarding strategies to enhance patient outcomes and decision-making factors for pivotal timepoints in esketamine NS treatment. This modified Delphi panel (3 rounds) established expert consensus (≥80% agreement) from 30 European psychiatrists experienced in management of patients with TRD receiving esketamine NS. During the acute phase (4–12 weeks), modest/subjective reductions in core symptoms important to both patients and physicians supported esketamine NS continuation, especially with long disease course/resistance to multiple therapies. Consensus was reached that such a modest improvement during the acute phase should justify esketamine NS continuation (and supplementation of other treatment modalities with esketamine NS). Esketamine NS dose/frequency maximisation (84 mg weekly) was advocated for, to enhance acute phase outcomes, alongside strategies reflective of individual clinical characteristics. Monitoring in the continuation phase (6–9 months) should prioritise residual/fluctuating symptoms, changes in symptom severity, functional recovery status and comorbidity management/emergence. Should residual symptoms persist, dose/frequency escalation, among other all-phase options, were supported. Prolonging maintenance phase treatment (≥12 months) depended on the degree of clinical worsening when tapering, the risks/consequences of relapse, chronicity of the last depressive episode, residual symptoms and recurrence history. Across all phases, recommended treatment plans included integration of psychotherapy, optimisation of concomitant antidepressants/augmentation strategies, comorbidity management and strengthening support networks. Overall, the consensus advocated for an approach reflective of TRD complexities, prioritising meaningful outcomes for individual patients.
Keywords:
Delphi method
Assessment (patient outcome)
Decision-making (shared)
Treatment resistant depression
Esketamine nasal spray
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European Neuropsychopharmacology cover
European Neuropsychopharmacology
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