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An Implementation Science Assessment of Intranasal Esketamine's Limited Integration into Mainstream Psychiatric
Benjamin Anderson1, Megan O'Grady2
1Institute of Living, Hartford Hospital, Hartford, CT, USA. Benjamin.anderson@hhchealth.org.
The Journal of Behavioral Health Services & Research
|October 19, 2025
Summary
Treatment resistant depression (TRD) affects many, but intranasal esketamine, approved in 2019, is underutilized. This review examines implementation barriers using CFIR and proposes solutions to improve patient access to this vital treatment.
Area of Science:
- Psychiatry
- Pharmacology
- Implementation Science
Background:
- Major Depressive Disorder (MDD) is a prevalent global mental illness.
- Treatment-resistant depression (TRD) describes patients unresponsive to standard antidepressant therapies.
- Intranasal esketamine received FDA approval in 2019 for TRD, offering a new therapeutic avenue.
Purpose of the Study:
- To analyze the limited real-world implementation of intranasal esketamine for TRD.
- To identify barriers to esketamine's adoption in psychiatric settings.
- To propose strategies for enhancing treatment accessibility.
Main Methods:
- Review of intranasal esketamine's real-world effectiveness studies.
- Application of the Consolidated Framework for Implementation Research (CFIR).
- Analysis of factors influencing clinical practice adoption.
Main Results:
- Despite proven efficacy, intranasal esketamine is not widely available in psychiatric settings.
- Implementation barriers exist across various domains, including policy, organizational, and individual levels.
- Limited accessibility hinders treatment for patients with TRD.
Conclusions:
- Addressing implementation barriers is crucial for equitable access to intranasal esketamine.
- Strategic interventions are needed to integrate esketamine into routine psychiatric care.
- Improved access can significantly benefit patients suffering from treatment-resistant depression.
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