For referring providers
Interventional psychiatry referrals: TMS and Spravato
Cognifica Health offers TMS therapy and Spravato (esketamine) as the next clinical step for patients who have not achieved adequate response with standard antidepressant treatment. Workers compensation approved. Two locations across Long Island and Westchester.
- Multidisciplinary teamNeurology, psychiatry & care coordination
- Insurance acceptedMedicare, Tricare, most major plans
- Virtual visitsTelehealth for qualifying services
- 2 locationsLong Island and Westchester, NY
- 500+ patientsTrusted by families since 2018
When to refer
TMS referral criteria
- Major Depressive Disorder with inadequate response to two or more antidepressant trials (adequate dose and duration)
- OCD with inadequate response to first-line treatment — TMS cleared as adjunct
- Anxious depression (MDD with comorbid anxiety symptoms)
- Patients who cannot tolerate antidepressant side effects — TMS is a non-medication alternative, not only a last resort after medication failure
- Adolescents aged 15 to 21 with treatment-resistant depression (FDA cleared 2024, adjunct treatment)
- Workers compensation patients with documented depression — TMS is approved for these patients at Cognifica Health
- Patients seeking non-pharmacologic treatment
Spravato referral criteria
- Treatment-Resistant Depression (TRD): inadequate response to two or more antidepressants of different classes at adequate doses for adequate duration
- MDD with acute suicidal ideation or behavior requiring rapid reduction of depressive symptoms
- Patients who cannot tolerate or have contraindications to oral antidepressants — 2025 monotherapy approval allows Spravato without a concurrent antidepressant
- Patients who have previously responded to ketamine infusions and prefer an FDA approved and insurance-covered alternative
- High-acuity cases where speed of response is clinically important — improvement documented as early as 24 hours post-dose
TMS clinical summary
TMS uses brief magnetic pulses comparable in strength to MRI fields to stimulate targeted cortical regions. The following summarizes the evidence base and protocol as used at Cognifica Health.
Evidence base
- Real-world response rate
- 58–78% (significant symptom reduction)
- Real-world remission rate
- 30–37%
- Durability
- Approximately 68% of responders maintain improvement at 12 months post-treatment
- Seizure risk
- <0.1% — comparable to antidepressant medication risk
- Primary data source
- PMC11234753 — multi-site psychiatric group practice registry
Protocol and FDA status
- FDA status
- Cleared — MDD (adults 2008, adolescents 15-21 adjunct 2024), OCD adjunct, anxious depression
- Session length
- 20 to 40 minutes
- Treatment course
- 5 sessions per week for 4 to 6 weeks (30–36 sessions total)
- Anesthesia required
- No — patients remain fully alert and can drive
- Medication interactions
- None — TMS can be used concurrently with current medications
- Contraindications
- Non-removable conductive metal in or near the head; prior seizure history requires evaluation
Workers comp approved
Workers compensation has already approved TMS for Cognifica Health patients. Relevant for occupational medicine physicians, pain management providers, and case managers where depression is a secondary documented condition.
Two active TMS sites
TMS is available at both our Aquebogue (Long Island) and West Harrison (Westchester) locations. Geographic coverage for referrals across both service areas.
All three FDA-cleared indications
Cognifica Health treats patients under all three TMS clearances: Major Depressive Disorder, OCD (adjunct), and anxious depression. The 2024 adolescent clearance (ages 15 to 21) is also available.
Non-medication candidate pathway
TMS is appropriate not only for patients who have failed medications, but for patients who cannot tolerate medication side effects — an underserved and often overlooked referral category.
Spravato clinical summary
Spravato (esketamine) is an NMDA receptor antagonist — pharmacologically distinct from monoaminergic antidepressants. The following summarizes the evidence base, FDA status, and administrative requirements.
FDA approval history
- March 2019
- TRD in conjunction with oral antidepressant (NDA 211243)
- August 2020
- MDD with acute suicidal ideation or behavior — in conjunction with oral antidepressant
- January 2025
- TRD as monotherapy — first FDA approved antidepressant monotherapy of its mechanism class
Clinical data and REMS
- Onset of action
- Measurable improvement in MADRS total score as early as 24 hours post-dose
- Monotherapy remission (week 4)
- 22.5% vs. 7.6% placebo (NCT04599855)
- Relapse prevention
- SUSTAIN-1: significantly delayed relapse in responders vs. placebo
- REMS requirement
- Certified healthcare setting only; 2-hour post-dose observation mandatory
- Administration
- Patient self-administers under direct provider supervision; prescriber must be licensed APRN, PA, or physician
- Common adverse effects
- Dissociation, dizziness, nausea, sedation, hypertension — typically resolve within the observation period
REMS certified treatment site
Cognifica Health is a REMS certified Spravato treatment site — a federal requirement for any practice administering esketamine. Not all psychiatric practices qualify.
2025 monotherapy approval
The January 2025 FDA approval allows Spravato to be used without a concurrent oral antidepressant. Patients who have failed or cannot tolerate oral antidepressants now have a monotherapy pathway.
Rapid onset for high-acuity cases
Clinical data show measurable improvement in depressive symptoms as early as 24 hours after the first dose. Spravato is also approved for MDD with acute suicidal ideation or behavior, making it relevant for patients requiring rapid clinical response.
Supervised in-office administration
All Spravato sessions are supervised by Susan Mogan, PMHNP, under the oversight of Dr. John Abrahams, MD. Patients remain on-site for a minimum of two hours per session.
Workers compensation pathway
TMS approved for workers comp patients at Cognifica Health
Workers compensation has already approved TMS for patients at Cognifica Health. This is a meaningful clinical pathway for occupational medicine physicians, pain management providers, and workers compensation case managers.
Depression as a secondary condition following workplace injury is well documented in the literature and is routinely underdiagnosed and undertreated in workers comp populations. TMS offers an evidence-based, non-medication intervention that workers comp carriers have recognized as appropriate treatment.
B2B referral targets
Provider categories that have referred successfully to Cognifica Health for TMS and Spravato:
- →Primary care physicians
- →Occupational medicine physicians
- →Pain management specialists
- →Neurologists
- →Psychologists (non-prescribing)
- →Licensed clinical social workers
- →Workers compensation case managers
- →Substance use treatment programs
Referral process
Contact our office
Call (914) 948 3008 (Westchester) or (631) 388 7624 (Long Island) to discuss a referral. Our clinical coordinator will confirm candidacy criteria and insurance before the patient is scheduled.
Send referral packet
Include: diagnosis, prior medication trials with doses and durations, relevant medical history, current medication list, and any prior neuropsychological testing. Fax or coordinate directly with our office.
Patient intake
Your patient completes a one-hour intake with Susan Mogan, PMHNP. No pre-screening call is required. Intake can be in-person or via telehealth.
Communication back to you
With patient authorization, we send clinical updates at intake, treatment initiation, and course completion. We are available for consultation throughout the treatment period.
Insurance accepted
Confirmed in-network
- Medicare
- Workers compensation
- No-fault insurance
- United Healthcare
Pending enrollment
Blue Cross Blue Shield, Aetna, Cigna, Health First, Fidelis, Medicaid, UMR, World Trade Center benefit fund
Out-of-network patients can receive a super bill. TMS and Spravato are HSA and FSA eligible expenses.
Contact for clinical questions
Dr. John Abrahams, MD and Susan Mogan, PMHNP
For clinical questions about a specific patient, call our office directly. We are available for provider-to-provider consultation.
- Westchester: (914) 948 3008
- Long Island: (631) 388 7624
Start a referral
Send us a referral inquiry
Fill in your contact details and what you are referring for. Our clinical coordinator will follow up within one business day to confirm candidacy and next steps. No patient information is collected here.
Prefer to call?
- Westchester: (914) 948 3008
- Long Island: (631) 388 7624
Provider-to-provider consultations available by phone.
Provider questions
Sources and References
- FDA 510(k) K083538 — NeuroStar TMS Clearance (2008)
- Utilization and outcomes of TMS and usual care for MDD — PMC11234753
- Clinical TMS Society Consensus Review — PMC5612370
- FDA NDA 211243 — Spravato (esketamine) Approval History
- Spravato Monotherapy Approval — J&J Press Release (January 2025)
- Spravato HCP Prescribing Information