Spravato® (Esketamine) Therapy
in West Hartford, CT
A breakthrough nasal spray for adults with treatment-resistant depression. Administered and monitored on-site at our West Hartford office. Now FDA-approved as a standalone treatment - no concurrent oral antidepressant required.
What Is Treatment-Resistant Depression?
Treatment-resistant depression (TRD) is diagnosed when a person has tried at least two different antidepressants at adequate doses and durations without meaningful improvement. It affects an estimated 30% of people with major depressive disorder.
TRD is not a personal failure - it reflects a biological reality that standard medications don't fully address. The brain's glutamate signaling pathways, which antidepressants often don't target, may be a key factor. Esketamine works differently, acting on NMDA receptors in those pathways.
If you've been living with depression despite trying multiple medications, Spravato® may be a path forward.
How Spravato® Works
Esketamine takes a fundamentally different approach than traditional antidepressants.
Different Mechanism
Traditional antidepressants affect serotonin, norepinephrine, or dopamine. Esketamine blocks NMDA receptors and rapidly increases synaptic connections in the prefrontal cortex - areas linked to mood regulation.
Rapid Onset
Many patients report improvement within hours to days of their first session - not the 4 - 6 weeks required for most oral antidepressants. For those in acute distress, this speed matters significantly.
FDA Approved
Spravato® received initial FDA approval in 2019 as an adjunct treatment for TRD. In January 2025, the FDA expanded approval to include monotherapy use - making it the only intranasal treatment FDA-approved for treatment-resistant depression as a standalone option.
Standalone or Combined
In January 2025, the FDA approved Spravato® as the first and only monotherapy for treatment-resistant depression - meaning it can now be used on its own, without requiring a concurrent oral antidepressant. It can also be combined with an oral antidepressant for patients who benefit from both.
What to Expect at a Session
Each Spravato® session takes place entirely at our West Hartford office. You'll need to arrange a ride home - you cannot drive the day of treatment. Plan for approximately 2.5 - 3 hours total.
Who May Qualify for Spravato®
Spravato® is FDA-approved for adults who meet specific criteria. At your consultation, Dr. Heidari will review your full psychiatric and medication history to determine if you're a good candidate.
Insurance & Financial Assistance
Most major commercial insurance plans and Medicare cover Spravato®. We work with you to verify benefits before your first session.
Commercial Insurance
Most major plans - Aetna, Cigna, UnitedHealthcare, Anthem Blue Cross Blue Shield - typically cover Spravato® when TRD criteria are documented. Prior authorization is usually required; we handle that process.
Medicare & Medicaid
Medicare Part D covers Spravato® for qualifying beneficiaries. Medicaid coverage varies by state; Connecticut's Husky plan covers it in many cases. We verify your specific plan before scheduling.
Janssen CarePath Assistance
Janssen Pharmaceuticals offers the Spravato® CarePath patient assistance program for uninsured or underinsured patients. Eligible patients may pay as little as $10 per session. Ask us about enrollment.
Spravato® FAQs
Ready to Learn If Spravato® Is Right for You?
Call our West Hartford office to speak with a member of our clinical team, or book a consultation online. We typically respond within one business day.
Spravato® is a registered trademark of Janssen Pharmaceuticals. Individual results vary. This page is for informational purposes only and does not constitute medical advice.