# Standard Operating Procedure: TMS Treatment Protocol | Document ID | SOP-TMS-001 | |-------------|-------------| | Title | Transcranial Magnetic Stimulation Treatment Protocol | | Revision | 1.0 | | Effective Date | [DATE] | | Author | [AUTHOR] | | Approved By | [APPROVER] | | Department | TMS Clinic | --- ## 1. Purpose To establish standardized procedures for the safe and effective administration of Transcranial Magnetic Stimulation (TMS) therapy in accordance with FDA clearances, manufacturer guidelines, and clinical best practices. ## 2. Scope This procedure applies to all TMS treatments including: - Repetitive TMS (rTMS) for Major Depressive Disorder - rTMS for Obsessive-Compulsive Disorder - Intermittent Theta Burst Stimulation (iTBS) - Other FDA-cleared or investigational protocols ## 3. Responsibilities ### 3.1 TMS Technician/Operator - Position patient and equipment - Determine motor threshold - Administer treatment per prescription - Monitor patient during treatment - Document treatment parameters ### 3.2 Prescribing Physician - Evaluate patient eligibility - Prescribe treatment protocol - Review progress and adjust treatment - Manage adverse events - Provide medical oversight ### 3.3 Clinical Coordinator - Schedule treatments - Track treatment compliance - Coordinate patient assessments - Maintain equipment logs ## 4. Definitions | Term | Definition | |------|------------| | MT | Motor Threshold - minimum intensity to produce MEP | | MEP | Motor Evoked Potential - observable motor response | | rTMS | Repetitive Transcranial Magnetic Stimulation | | iTBS | Intermittent Theta Burst Stimulation | | DLPFC | Dorsolateral Prefrontal Cortex - common target for depression | ## 5. Equipment and Materials - TMS device (FDA-cleared) - Treatment coil (figure-8 or appropriate for indication) - Positioning chair or table - Ear protection (ear plugs) - Treatment cap or head marking system - Motor threshold determination tools - Emergency equipment (as per emergency SOP) ## 6. Procedure ### 6.1 Pre-Treatment Assessment #### 6.1.1 Initial Evaluation (First Treatment) 1. **Verify Prescription** - Diagnosis confirmed - Treatment protocol specified - Contraindications reviewed - Informed consent on file 2. **Safety Screening** Confirm absence of contraindications: - [ ] No ferromagnetic metal in head/neck - [ ] No implanted devices (pacemaker, cochlear implant, DBS) - [ ] No history of seizures (unless per protocol) - [ ] No unstable medical conditions - [ ] Current medications reviewed for seizure threshold effects - [ ] Pregnancy test negative (if applicable) 3. **Baseline Assessments** - PHQ-9 or HAM-D (depression) - Y-BOCS (OCD, if applicable) - Vital signs - Cognitive baseline if indicated #### 6.1.2 Daily Pre-Treatment Check Before each session: - [ ] Patient identity verified - [ ] Assess for new contraindications - [ ] Confirm adequate sleep (>4 hours) - [ ] Confirm no alcohol/illicit substances - [ ] Confirm no significant medication changes - [ ] Assess for current illness - [ ] Review previous session tolerance ### 6.2 Motor Threshold Determination **Required at:** - First treatment session - Any significant change in medications affecting neural excitability - If treatment efficacy changes significantly - Per physician order **Procedure:** 1. Position patient comfortably 2. Place coil over motor cortex (M1) contralateral to dominant hand 3. Begin at 30-40% machine output 4. Deliver single pulses at 10-second intervals 5. Observe for thumb/finger movement (APB) 6. Increase intensity by 5% increments 7. Record lowest intensity producing 5 MEPs in 10 trials 8. Document MT and method used | MT Parameter | Value | |--------------|-------| | Date | | | Resting Motor Threshold (%) | | | Target Muscle | | | Number of Trials | | | Determined By | | ### 6.3 Treatment Coil Positioning #### 6.3.1 Left DLPFC Targeting (Standard Depression Protocol) **5-cm Rule Method:** 1. Identify motor hotspot (from MT determination) 2. Measure 5 cm anteriorly along scalp surface 3. Mark position on treatment cap 4. Verify coil angle (45° to midline) **Neuronavigation Method (if available):** 1. Register patient to MRI 2. Identify target coordinates 3. Position coil using navigation system 4. Document coordinates and trajectory #### 6.3.2 Alternative Targets - Right DLPFC (low-frequency protocol) - Supplementary Motor Area (OCD) - Other per protocol specification ### 6.4 Treatment Administration 1. **Patient Preparation** - Seat in treatment chair - Provide ear protection - Position head comfortably - Instruct patient on what to expect 2. **Equipment Setup** - Power on device and perform calibration - Select prescribed protocol - Set treatment parameters: | Parameter | Value | |-----------|-------| | Frequency (Hz) | | | Intensity (% MT) | | | Pulses per train | | | Inter-train interval | | | Total pulses | | | Duration | | 3. **Treatment Delivery** - Position coil at marked location - Maintain consistent coil contact - Begin treatment delivery - Monitor patient continuously - Pause if patient reports concerning symptoms 4. **Patient Monitoring During Treatment** Observe for: - Facial twitching (may indicate coil drift) - Signs of distress - Seizure warning signs - Excessive discomfort ### 6.5 Standard Treatment Protocols #### Major Depressive Disorder - Standard rTMS | Parameter | Left DLPFC | |-----------|------------| | Frequency | 10 Hz | | Intensity | 120% MT | | Train duration | 4 seconds | | Inter-train interval | 26 seconds | | Trains per session | 75 | | Total pulses | 3,000 | | Session duration | ~37.5 minutes | | Total sessions | 30-36 | #### Major Depressive Disorder - iTBS | Parameter | Left DLPFC | |-----------|------------| | Pattern | 50 Hz bursts at 5 Hz | | Intensity | 120% MT | | Bursts per train | 10 (30 pulses) | | Inter-train interval | 8 seconds | | Total pulses | 600 | | Session duration | ~3 minutes | | Total sessions | 30-36 | ### 6.6 Post-Treatment 1. **Immediate Assessment** - Ask about side effects - Assess for headache, scalp pain - Evaluate mental status - Confirm safe to leave 2. **Documentation** Complete FRM-TMS-001 Treatment Log: - Date and session number - Treatment parameters used - Coil position - Patient tolerance - Any adverse effects - Operator signature 3. **Patient Instructions** - Mild headache/scalp discomfort common - OTC analgesics acceptable - Report severe/persistent symptoms - Confirm next appointment ### 6.7 Adverse Event Management | Event | Severity | Action | |-------|----------|--------| | Scalp discomfort | Mild | Adjust position, OTC analgesic | | Headache | Mild-Moderate | OTC analgesic, reduce intensity if persistent | | Syncope | Moderate | Stop treatment, lie patient down, assess vitals | | Seizure | Severe | Stop treatment, protect patient, follow seizure protocol | **Seizure Response:** 1. Stop stimulation immediately 2. Note time 3. Protect patient from injury 4. Do not restrain 5. Call for help / activate emergency protocol 6. Monitor airway and breathing 7. Time seizure duration 8. Notify physician immediately 9. Complete incident report ## 7. Outcome Monitoring | Assessment | Timing | Tool | |------------|--------|------| | Depression severity | Weekly | PHQ-9 or HAM-D | | OCD severity (if applicable) | Weekly | Y-BOCS | | Side effects | Each session | TMS side effect checklist | | Treatment response | Sessions 10, 20, 30 | Physician evaluation | | Remission assessment | End of acute course | Full clinical evaluation | ## 8. Documentation - FRM-TMS-001 TMS Treatment Log - FRM-TMS-002 Motor Threshold Record - FRM-TMS-003 Side Effect Checklist - Outcome assessment forms - Equipment maintenance logs ## 9. References - FDA clearance documentation - Manufacturer operating manual - Clinical practice guidelines (APA, CANMAT) - Peer-reviewed TMS literature --- ## Revision History | Rev | Date | Description | Author | |-----|------|-------------|--------| | 1.0 | [DATE] | Initial release | [AUTHOR] |