Transcranial Magnetic Stimulation (TMS)
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Covers clinical background, FDA status, devices, and evidence for use of transcranial magnetic stimulation for behavioral health conditions (primarily major depressive disorder, OCD, and migraine with aura). Affects providers requesting coverage or prior authorization for TMS services under Providence Health Plan.
No material clinical or coverage changes in this revision.
Coverage Criteria and Positioning
Coverage rationale and criteria
Coverage and clinical positioning are informed by available evidence and device approvals; statements emphasize use in treatment‑resistant depression and specific cleared indications.
Supports use primarily where evidence and device clearance align (e.g., MDD, OCD, migraine with aura); emerging techniques without FDA approval (precuneus stimulation) are considered experimental.
See coding/device lists for FDA-cleared devices per indication.
Hayes and HTAs report mixed quality; Washington State HTA found moderate-to-high SOE for MDD while other reviews rate evidence as low to fair.
Coverage for Major Depressive Disorder (MDD)
Covered when clinical evidence and guideline recommendations are met for Major Depressive Disorder (MDD):
Based on guideline consensus (NNDC/Clinical TMS Society, VA/DoD) and evidence summaries; providers should document prior pharmacotherapy trials and treatment resistance.
Other conditions and maintenance therapy
Other indications — coverage stance informed by evidence:
Hayes assigned a 'C' rating for add‑on use; evidence insufficient for monotherapy; NICE and some reviews recommend further research.
Additional high‑quality RCTs with standardized protocols are needed.
Hayes and other payer reviews judge maintenance evidence as very limited; clinicians should justify maintenance use on a case‑by‑case basis.
No FDA‑approved devices for this technique; small studies and short follow‑up limit conclusions.
Precuneus magnetic stimulation is an MRI‑guided, EEG‑informed rTMS approach that personalizes stimulation to the precuneus — a hub of the default mode network — and is being investigated for cognitive decline and Alzheimer‑related outcomes. There are no FDA‑approved devices for precuneus magnetic stimulation, and the technique remains an emerging, non‑established treatment.
Early and experimental TMS targets, including precuneus stimulation and other novel target strategies, have only small, heterogeneous studies with short follow‑up and variable protocols. Evidence is limited and inconsistent; therefore these early/experimental targets are considered investigational pending higher‑quality, longer‑term randomized data.
All unlisted procedure codes submitted for services addressed by this policy are reviewed for medical necessity, correct coding, and pricing. If an unlisted code is submitted for a non‑covered service addressed in this policy it will be denied as not covered; for potentially covered services prior authorization is recommended to avoid post‑service denial.
FDA clearance or approval of a device is provided for informational purposes and does not by itself establish medical necessity or guarantee coverage. FDA clearance alone is not sufficient to meet medical‑necessity requirements; treatments must also be supported by the evidence and indications described in this policy.
Maintenance repetitive transcranial magnetic stimulation (rTMS) delivered to prevent recurrence of major depressive disorder has been evaluated but the evidence is very limited and of low quality. Reviews have rated the evidence very low (D) and found inconsistent results versus sham or usual care; consequently maintenance rTMS is considered investigational / not sufficiently supported for recurrence prevention at this time.
Device and Procedure Coding
| Brainsway H-Coil Deep TMS System | Deep TMS system listed for Major Depressive Disorder |
| Neurostar TMS Therapy | TMS system listed for Major Depressive Disorder |
| Horizon 3.0 TMS Therapy | TMS system listed for Major Depressive Disorder |
| MagVita TMS Therapy System w/Theta Burst Stimulation | TMS system listed for Major Depressive Disorder |
| Nextstim Navigated Brain Therapy (NBT) System 2 | Listed device for Major Depressive Disorder |
| Rapid2 Therapy System | Listed device for Major Depressive Disorder |
| Neurosoft TMS | Listed device for Major Depressive Disorder |
| Brainsway Deep Transcranial Magnetic Stimulation System | Device listed for Obsessive Compulsive Disorder |
| Cerena Transcranial Magnetic Stimulator | Device listed for Migraine with Aura |
| SpringTMS® | Device listed for Migraine with Aura |
| Precuneus magnetic stimulation | Emerging technique; no FDA-approved devices |
| 0858T | Referenced / crosswalked code in accelerated/advanced TMS procedures (document lists equivalence relationships) |
| 0889T | Accelerated, repetitive high-dose functional connectivity MRI-guided theta-burst stimulation - initial (as referenced) |
| 0891T | Personalized target development for accelerated, repetitive high-dose fcMRI-guided theta-burst stimulation (as referenced) |
| 0892T | Accelerated, repetitive high-dose fcMRI-guided theta-burst stimulation - subsequent treatment day (as referenced) |
| 0997T | Subsequent motor threshold redetermination with delivery and management, per treatment day (as referenced) |
| 0998T | Precuneus magnetic stimulation; personalized treatment delivery per day (as referenced) |
| 90867 | Therapeutic repetitive transcranial magnetic stimulation (TMS) (as referenced) |
| 0858T | listed in mapping to multiple advanced/accelerated TMS procedures in this section |
| 0889T | mapped equivalent in document for personalized target development / accelerated protocols |
| 0891T | accelerated, repetitive high-dose functional connectivity MRI-guided theta-burst stimulation, initial treatment day (mapped) |
| 0892T | accelerated, repetitive high-dose functional connectivity MRI-guided theta-burst stimulation, subsequent treatment day (mapped) |
| 0997T | subsequent motor threshold redetermination with delivery and management, per treatment day (mapped) |
| 0998T | Precuneus magnetic stimulation; treatment planning using MRI-guided neuronavigation (mapped) |
| 90867 | Therapeutic repetitive transcranial magnetic stimulation (TMS) treatment; initial, including cortical mapping, motor threshold determination, delivery and management |
| 90868 | Therapeutic repetitive transcranial magnetic stimulation (TMS) treatment; subsequent delivery and management, per session |
| 90869 | Therapeutic repetitive transcranial magnetic stimulation (TMS) treatment; subsequent motor threshold re-determination with delivery and management |
Prior Authorization, Documentation, and Billing Rules
Prior authorization depends on medical necessity and indication
Coverage and prior authorization decisions for TMS are based on demonstrated medical necessity and the specific indication; the policy lists FDA-cleared devices by indication to inform device–indication alignment during review.
- FDA clearance alone does not establish medical necessity; coverage requires demonstrated medical necessity for the indicated diagnosis.
- Providers should align requested device use with the FDA-cleared device list by indication (MDD, OCD, migraine with aura).
Prior authorization may be required for listed TMS procedure codes
Certain TMS CPT/HCPCS procedure codes are identified as affected and services billed under these codes may require prior authorization; billing rules also require physician oversight for daily TMS sessions.
Prior authorization and review recommended for unlisted codes
Unlisted procedure codes are subject to review for medical necessity, correct coding, and pricing; prior authorization is recommended for unlisted codes submitted for potentially covered services to avoid post-service denial.
- All unlisted codes are reviewed at the claim level for medical necessity, coding, and pricing.
- If an unlisted code is submitted for a potentially covered service, prior authorization is recommended to avoid post-service denial.
Document prior pharmacotherapy / treatment resistance
When requesting TMS for treatment-resistant depression, document prior pharmacologic trials or treatment resistance; the policy notes an emerging consensus to consider TMS after failure of at least two antidepressant medication trials.
- Document the history of prior antidepressant trials (failure to respond to at least two trials is the commonly cited threshold).
- Record whether TMS is being used as augmentation or primary therapy and relevant treatment timelines.
Position TMS after inadequate pharmacologic response (commonly ≥2 trials)
TMS is generally positioned after inadequate response to pharmacologic treatments for major depressive disorder; guidance and evidence commonly reference considering TMS after ≥2 antidepressant trials.
- VA/DoD guideline suggests offering rTMS for patients with partial or no response to an adequate trial of 2 or more pharmacologic treatments.
- Emerging consensus recommends considering TMS for patients who have failed to respond to at least two antidepressant medication trials.
Submit complete clinical documentation: indication, device, device–indication mapping, and prior treatments
Ensure required clinical and billing documentation is complete: document the indication, device used (or note experimental techniques), FDA-cleared device mapping to indication, and prior treatment history to support medical necessity.
- Document the patient diagnosis (e.g., MDD, OCD, migraine with aura) and whether treatment is augmentation or primary.
- Specify the device used and align it to the policy's list of FDA-cleared devices for the indicated condition; note if the technique/device is experimental (e.g., precuneus stimulation).
- Include prior treatment history (pharmacologic trials, durations, and outcomes) to substantiate treatment-resistance claims.
Supervising clinician must perform initial evaluation; operators require documented training
Initial evaluation and treatment planning must be performed by the supervising psychiatrist or psychiatric mental health nurse practitioner (PMHNP); device operators must have documented training and maintained competency.
- Supervising clinician must perform the initial evaluation and treatment planning directly and cannot delegate this responsibility.
- Operators should be trained in motor threshold assessment, coil positioning, patient monitoring, and emergency response and maintain documented competency.
Initial evaluation cannot be delegated; PA/NP billing must be 'incident to' supervising physician
For billing and provider roles: initial evaluation and treatment planning cannot be delegated; PAs/NPs may not bill independently for daily TMS sessions and such services must be billed 'incident to' a supervising physician per applicable billing guidelines.
- Initial evaluation and treatment planning must be performed directly by the supervising psychiatrist or PMHNP and cannot be delegated.
- Daily TMS session administration by PAs/NPs must be billed 'incident to' a supervising physician; PAs/NPs may not bill independently for these services.
Unlisted code review and denial risk for non-covered services
All unlisted codes submitted for services addressed by this policy are reviewed for medical necessity, coding accuracy, and pricing; submissions for non-covered services will be denied as not covered.
- Unlisted codes for potentially covered services: prior authorization is recommended to avoid post-service denial.
- If an unlisted code is submitted for a non-covered service addressed in this policy, it will be denied as not covered.
FDA clearance does not equal medical necessity — document clinical justification
FDA clearance alone does not establish medical necessity and is not sufficient for coverage; absence of documented medical necessity or insufficient evidence for the requested indication may result in denial.
- Approval or clearance by the FDA does not itself establish medical necessity or serve as a basis for coverage.
- Treatments lacking sufficient evidence for the requested indication or long-term benefit may be deemed not medically necessary.
PA/NP billing limits and daily TMS session billing guidance
Billing limitations and daily session billing guidance: PAs and NPs may not bill independently for TMS daily sessions (must be billed 'incident to'); initial evaluation/treatment planning must be done by the supervising psychiatrist or PMHNP and cannot be billed by delegation.
- Daily TMS session administration must be billed 'incident to' a supervising physician; PAs/NPs cannot bill independently for these services.
- Ensure billing codes reflect that initial evaluation and treatment planning were performed by the supervising psychiatrist or PMHNP.
Unlisted code submissions for non-covered services will be denied
Submission of an unlisted code for a non-covered service addressed by this policy will be denied as not covered; prior authorization is recommended for unlisted codes submitted for potentially covered services to avoid post-service denial.
- Unlisted codes submitted for non-covered services will be denied.
- Prior authorization is recommended when unlisted codes are used for potentially covered services.
Clinical Background and Definitions
Repetitive transcranial magnetic stimulation (rTMS) is a noninvasive neuromodulation technique that applies repeated magnetic pulses to the scalp to modulate cortical electrical activity and influence neural circuits involved in mood and cognitive function. It can be delivered as conventional rTMS, patterned protocols such as theta‑burst stimulation, or as MRI‑guided/accelerated approaches; clinical use is most extensively studied for major depressive disorder, with other indications supported by more limited evidence.
Level of Care and Setting
Outpatient — level-of-care criteria (top-level nodes present in source)
Reflects guideline recommendations for prescriber/operator qualifications and documentation of prior pharmacotherapy/trials.
Guidelines recommend monitoring and individualized maintenance planning; durability of effect is uncertain.
Outpatient — additional outpatient criteria chunk
Aligns with Clinical TMS Society/NNDC recommendations for clinician and operator qualifications.
Step therapy guidance suggests documenting ≥2 failed antidepressant trials for TRD populations.
Modalities and Techniques
TMS — primary treatment modality criteria node
See background/definitions for modality description; coding guidance applies for billing and prior authorization.
TMS / accelerated rTMS / precuneus stimulation — modality group including accelerated and precuneus approaches
Hayes evolving evidence review (2023) concluded protocols are safe but not yet supported as recommended treatments; clinical discretion required.
Small studies and short follow‑up limit conclusions; excluded from coverage absent explicit authorization.
TMS / rTMS / theta-burst — criteria group for theta-burst and rTMS variants
Some systematic reviews describe TBS as 'potentially effective' but call for longer‑term and standardized protocol studies; coding crosswalks exist for accelerated/theta‑burst procedures.
See billing/coding section for code mappings (0858T, 0889T, 0891T, 0892T, 0997T, 0998T, 90867–90869) and prior authorization guidance.
Maintenance and Visit Limit Notes
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